(en)The present relation relates to a transgenic Vero cell line expressing CD4 and CCR5. The present invention encompasses the preparation and purification of immunogenic compositions which are formulated into the vaccines of the present invention.

1.ApplicationNumber: US-201715481108-A
1.PublishNumber: US-2017266272-A1
2.Date Publish: 20170921
3.Inventor: PARKS CHRISTOPHER L.
KOFF WAYNE C.

4.Inventor Harmonized: PARKS CHRISTOPHER L(US)
KOFF WAYNE C(US)

5.Country: US
6.Claims:
(en)The present relation relates to a transgenic Vero cell line expressing CD4 and CCR5. The present invention encompasses the preparation and purification of immunogenic compositions which are formulated into the vaccines of the present invention.

7.Description:
(en)INCORPORATION BY REFERENCE
This application is a continuation-in-part application of U.S. patent application Ser. No. 15/280,710 filed Sep. 29, 2016, which claims benefit of and priority to U.S. provisional patent application Ser. No. 62/236,448 filed Oct. 2, 2015.
The foregoing applications, and all documents cited therein or during their prosecution (“appln cited documents”) and all documents cited or referenced herein (“herein cited documents”), and all documents cited or referenced in herein cited documents, together with any manufacturer's instructions, descriptions, product specifications, and product sheets for any products mentioned herein or in any document incorporated by reference herein, are hereby incorporated herein by reference, and may be employed in the practice of the invention.


SEQUENCE LISTING
The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy, created on May 10, 2017, is named 43094_02_2039_SL.txt and is 57,121 bytes in size.
FIELD OF THE INVENTION
The present invention relates to a transgenic Vero cell line expressing CD4 and CCR5 for use to manufacture prophylactic and therapeutic vaccines.
BACKGROUND OF THE INVENTION
AIDS, or Acquired Immunodeficiency Syndrome, is caused by human immunodeficiency virus (HIV) and is characterized by several clinical features including wasting syndromes, central nervous system degeneration and profound immunosuppression that results in opportunistic infections and malignancies. HIV is a member of the lentivirus family of animal retroviruses, which include the visna virus of sheep and the bovine, feline, and simian immunodeficiency viruses (SIV). Two closely related types of HIV, designated HIV-1 and HIV-2, have been identified thus far, of which HIV-1 is by far the most common cause of AIDS. However, HIV-2, which differs in genomic structure and antigenicity, causes a similar clinical syndrome.
An infectious HIV particle consists of two identical strands of RNA, each approximately 9.2 kb long, packaged within a core of viral proteins. This core structure is surrounded by a phospholipid bilayer envelope derived from the host cell membrane that also includes virally-encoded membrane proteins (Abbas et al., Cellular and Molecular Immunology, 4th edition, W.B. Saunders Company, 2000, p. 454). The HIV genome has the characteristic 5′-LTR-Gag-Pol-Env-LTR-3′ organization of the retrovirus family. Long terminal repeats (LTRs) at each end of the viral genome serve as binding sites for transcriptional regulatory proteins from the host and regulate viral integration into the host genome, viral gene expression, and viral replication.
The HIV genome encodes several structural proteins. The gag gene encodes structural proteins of the nucleocapsid core and matrix. The pol gene encodes reverse transcriptase (RT), integrase (IN), and viral protease (PR) enzymes required for viral replication. The tat gene encodes a protein that is required for elongation of viral transcripts. The rev gene encodes a protein that promotes the nuclear export of incompletely spliced or unspliced viral RNAs. The vif gene product enhances the infectivity of viral particles. The vpr gene product promotes the nuclear import of viral DNA and regulates G2 cell cycle arrest. The vpu and nef genes encode proteins that down regulate host cell CD4 expression and enhance release of virus from infected cells. The env gene encodes the viral envelope glycoprotein that is translated as a 160-kilodalton (kDa) precursor (gp160) and cleaved by a cellular protease to yield the external 120-kDa envelope glycoprotein (gp120) and the transmembrane 41-kDa envelope glycoprotein (gp41), which are required for the infection of cells (Abbas, pp. 454-456). gp140 is a modified form of the Env glycoprotein, which contains the external 120-kDa envelope glycoprotein portion and the extracellular part of the gp41 portion of Env and has characteristics of both gp120 and gp41. The nef gene is conserved among primate lentiviruses and is one of the first viral genes that is transcribed following infection. In vitro, several functions have been described, including down-regulation of CD4 and MHC class I surface expression, altered T-cell signaling and activation, and enhanced viral infectivity.
HIV infection initiates with gp120 on the viral particle binding to the CD4 and chemokine receptor molecules (e.g., CXCR4, CCR5) on the cell membrane of target cells such as CD4 + T-cells, macrophages and dendritic cells. The bound virus fuses with the target cell and reverse transcribes the RNA genome. The resulting viral DNA integrates into the cellular genome, where it directs the production of new viral RNA, and thereby viral proteins and new virions. These virions bud from the infected cell membrane and establish productive infections in other cells. This process also kills the originally infected cell. HIV can also kill cells indirectly because the CD4 receptor on uninfected T-cells has a strong affinity for gp120 expressed on the surface of infected cells. In this case, the uninfected cells bind, via the CD4 receptor-gp120 interaction, to infected cells and fuse to form a syncytium, which cannot survive. Destruction of CD4 + T-lymphocytes, which are critical to immune defense, is a major cause of the progressive immune dysfunction that is the hallmark of AIDS disease progression. The loss of CD4 + T cells seriously impairs the body's ability to fight most invaders, but it has a particularly severe impact on the defenses against viruses, fungi, parasites and certain bacteria, including mycobacteria.
Research on the Env glycoprotein has shown that the virus has many effective protective mechanisms with few vulnerabilities (Wyatt & Sodroski, Science. 1998 Jun. 19; 280(5371):1884-8). For fusion with its target cells, HIV-1 uses a trimeric Env complex containing gp120 and gp41 subunits (Burton et al., Nat Immunol. 2004 March; 5(3):233-6). The fusion potential of the Env complex is triggered by engagement of the CD4 receptor and a coreceptor, usually CCR5 or CXCR4. Neutralizing antibodies seem to work either by binding to the mature trimer on the virion surface and preventing initial receptor engagement events, or by binding after virion attachment and inhibiting the fusion process (Parren & Burton, Adv Immunol. 2001; 77:195-262). In the latter case, neutralizing antibodies may bind to epitopes whose exposure is enhanced or triggered by receptor binding. However, given the potential antiviral effects of neutralizing antibodies, it is not unexpected that HIV-1 has evolved multiple mechanisms to protect it from antibody binding (Johnson & Desrosiers, Annu Rev Med. 2002; 53:499-518).
There remains a need to express immunogens that elicit broadly neutralizing antibodies. Strategies include producing molecules that mimic the mature trimer on the virion surface, producing Env molecules engineered to better present neutralizing antibody epitopes than wild-type molecules, generating stable intermediates of the entry process to expose conserved epitopes to which antibodies could gain access during entry and producing epitope mimics of the broadly neutralizing monoclonal antibodies determined from structural studies of the antibody-antigen complexes (Burton et al., Nat Immunol. 2004 March; 5(3):233-6). However, none of these approaches have yet efficiently elicited neutralizing antibodies with broad specificity.
Citation or identification of any document in this application is not an admission that such document is available as prior art to the present application.
SUMMARY OF THE INVENTION
The present invention relates to a transgenic Vero cell line that express CD4/CCR5. In an advantageous embodiment, the CD4/CCR5 is derived from either human or rhesus macaque. In an advantageous embodiment, the transgenic Vero-CD4/CCR5 cell lines support Env-dependent infection and replication by VSV- and CDV-Env chimeras, wherein the Env expressed by infected cells comprises a native conformation and antigenicity. The invention encompasses manufacturing of replicating viral vectored HIV vaccines that express functional Env immunogens. Because Vero is a FDA-approved cell substrate for human vaccine production, the transgenic Vero-CD4/CCR5 cell line is suitable for manufacturing human vaccines.
Transgenic Vero-CD4/CCR5 cells are useful for HIV vaccine production since many safety risks associated with cell substrates have been addressed for the Vero cell background. The unique CD4/CCR5 transgene design directs expression of a CCR5 and CD4 polyprotein linked by a 2A sequence (de Felipe P, Luke G A, Hughes L E, Gani D, Halpin C, Ryan M D. E unum pluribus: multiple proteins from a self-processing polyprotein. Trends Biotechnol. 2006; 24(2):68-75) that is subsequently self-cleaved resulting in 1 to 1 ratio of CD4 and CCR5 molecules.
The transgenic Vero-CD4/CCR5 cell lines are useful for producing replicating viral vectors expressing HIV or SIV Env. Their use can also be expanded for use in assays requiring cells expressing CD4 and CCR5.
As the expression cassette proved effective with CD4 and CCR5, it is useful for making cell lines expressing other polypeptides.
Accordingly, it is an object of the invention to not encompass within the invention any previously known product, process of making the product, or method of using the product such that Applicants reserve the right and hereby disclose a disclaimer of any previously known product, process, or method. It is further noted that the invention does not intend to encompass within the scope of the invention any product, process, or making of the product or method of using the product, which does not meet the written description and enablement requirements of the USPTO (35 U.S.C. §112, first paragraph) or the EPO (Article 83 of the EPC), such that Applicants reserve the right and hereby disclose a disclaimer of any previously described product, process of making the product, or method of using the product.
It is noted that in this disclosure and particularly in the claims and/or paragraphs, terms such as “comprises”, “comprised”, “comprising” and the like can have the meaning attributed to it in U.S. patent law; e.g., they can mean “includes”, “included”, “including”, and the like; and that terms such as “consisting essentially of” and “consists essentially of” have the meaning ascribed to them in U.S. patent law, e.g., they allow for elements not explicitly recited, but exclude elements that are found in the prior art or that affect a basic or novel characteristic of the invention.
These and other embodiments are disclosed or are obvious from and encompassed by, the following Detailed Description.



BRIEF DESCRIPTION OF THE DRAWINGS
The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.
The following detailed description, given by way of example, but not intended to limit the invention solely to the specific embodiments described, may best be understood in conjunction with the accompanying drawings, in which:
FIGS. 1A-1C . Recombinant VSVΔG-Env. A) A linear map of the VSV genome, which contains 5 gene regions encoding the Nucleocapsid protein (N), the Phosphoprotein (P) RNA-dependent RNA polymerase subunit, Matrix protein (M), Glycoprotein (G), and the catalytic subunit of the polymerase (Large protein or L). The 11-kb RNA genome is single-stranded, nonsegmented, and negative-sense. A single promoter at the 3′ end controls mRNA synthesis. Transcription initiated at the 3′ end terminates and reinitiates at each gene boundary. Because reinitiation is not 100% efficient, gene regions distal to the promoter are transcribed less efficiently generating a protein expression gradient. Changing the gene order, particularly when N is placed downstream, attenuates virus replication. A schematic of the VSV particle is show next to the genome map. B) Genome of the VSVΔG-Env.BG505 chimera in which the G gene is replaced with sequence encoding HIV Env.BG505. C) Map of the VSVΔG-Env genomic clone. The VSV (Indiana serotype) genomic sequence was derived from a lab-adapted virus. The Env.BG505 gene sequence is optimized to reflect VSV codon usage and relatively A+T-rich nucleotide content. To support rescue of recombinant virus, the T7 bacteriophage promoter is positioned to transcribe a positive-sense genome copy precursor and subsequent cleavage by cis-acting ribozymes generate precise termini.
FIGS. 2A-2D . Summary of VSVΔG-Env.BG505 rescue and vaccine preparation. Steps in the process are summarized along with virus particle illustrations that show glycoprotein composition at different stages. Chimeric virus rescue is initiated by electroporating DNA (A) into Vero or VeroCD4/CCR5 cells. Virus that buds from electroporated cells then is expanded using VeroCD4/CCR5 cells before conducting 3 rounds of clonal isolation (B). Clonal isolates are characterized, and candidates are selected for seed virus amplification and storage. Conducting these steps using CD4+/CCR5+ ensures that the vector is genetically stable and will propagate efficiently using Env. When a pseudotyped vaccine preparation is produced (C), virus infection is performed using VeroCD4/CCR5 cells electroporated with DNA encoding G. Replication in vivo (D) produces virus particles that lack the G glycoprotein.
FIGS. 3A-3B . Improvement of Env spike surface expression. A) Flow cytometry conducted with transfected 293T cells expressing modified Envs. Monoclonal bnAbs used for detection are indicated at the right. Notably, antibodies PG16, PGT151, and PGT145 preferentially react with epitopes that are formed by well-ordered trimers. A linear illustration of an Env monomer and corresponding Env-G hybrids (B) is shown below the flow cytometry data in Part A. SP, signal peptide, which is cleaved during translational processing; TM, transmembrane; CT, cytoplasmic tail; MPER, the Env membrane proximal external region; G stem; membrane proximal external region of G.
FIGS. 4A-4C . Antigenicity of Env.BG505 trimers delivered with VSVΔG-Env.BG505. Chimeric virus particles containing Env.BG505 only (A) were used for analyses in panels C-D. In B, infected VeroCD4/CCR5 were analyzed by flow cytometry using antibodies listed on the X-axis. In C, purified virus was adsorbed to alum after which the alum-virus complexes were reacted with mAbs and analyzed by flow cytometry. The asterisks in B and C highlight antibodies that preferentially recognized well order trimers.
FIGS. 5A-5C . Immunogenicity of a prototype VSVΔG-SIV-GagEnv chimera in rhesus macaques. A) Genome map of the VSVΔG-SIV-GagEnv chimera, which contains the SIV Gag and Env genes. The C-terminus of Env was truncated leaving a six-amino acid cytoplasmic domain. This was required to improve express of SIV Env by the VSV vector. B) Three groups of animals (3 per group) were vaccinated with VSVΔG-SIV-GagEnv, VSVΔG-SIV-GagEnv prepared with a G pseudotype, or a negative control, which was live recombinant VSV. Animals were vaccinated twice (0 and 6 weeks) with 2×10 8 pfus. Live virus in buffered solution was administered in drops applied to the nasal and oral cavities (1×10 8 pfu per site). C) Anti-SIV Env serum antibody titers were quantified by bioplex assay. To the right side of the chart, the peak antibody titer elicited in an earlier study with a DNA-SIV Env prime (electroporation) and Ad5-SIV Env boost is indicated with a dotted line for comparison. Assay background is subtracted from the data presented in the graph.
FIGS. 6A-6C . Genome maps comparing VSVΔG-Env.BG505 and an alternative vector design, VSV-G6-Env.BG505. A) The VSVΔG-Env.BG505 chimera genome contains 5 genes with Env.BG505 coding sequence inserted in place of G (position 4, also see FIG. 1 ). Gene expression declines with increasing distance from the transcriptional promoter located at the left end (yellow arrow, and see FIG. 1 ). The VSVΔG-Env.BG505 particle is illustrated with only Env incorporated on the surface, which is representative of the progeny virus particles that will be produced as the vector replicates in the vaccinee. B) In the VSV-G6-EnvBG505 vector, the G gene was reintroduced, but placed in position 6, which down-regulates G expression and enables stable coexpression of both glycoproteins. C) VSV schematic for comparison to the two vectors illustrated above.
FIG. 7 . Preclinical efficacy study design. Three groups of 10 Indian rhesus macaques were vaccinated according to the timeline at the top, which shows months and weeks. The three vaccine groups included: VSVΔG-Env.BG505 chimeria, VSV-G6-Env.BG505, and saline control. Vaccination and repeated rectal challenge time points are illustrated by filled triangles. Challenge was conducted with a heterologous clade B SHIV (SHIV SF162p3).
FIG. 8 . Serum antibodies elicited by vaccination. Antibody binding to Env.BG505 gp120 was quantified by ELISA over the course of the vaccination phase.
FIG. 9 . Monitoring SHIV genome copies in the blood of infected animals. SHIV genome copies in blood samples were quantified by real-time quantitative PCR (RT-qPCR). Genome copies per ml of plasma are plotted from the time infection was first detected by a qPCR signal of ≧200 genome copies per ml. Animal identifiers are located to the right of the graphs. Bold indicates infected animals through the 10th challenge.
FIG. 10 . SHIV infection rate during repetitive rectal challenge. As described in FIG. 7 , three groups of 10 animals were vaccinated with VSVΔG-Env.BG505 (red line), VSV-G6-Env.BG505 (blue line), or saline (black line). About 5 months after the third vaccination at week 48, challenge commenced using 2.2×10 4 TCID50 per rectal inoculation (TCID50: tissue culture infectious dose required to produce cytopathic effect in 50% of inoculated cell cultures). The graph shows the number of uninfected animals (Y axis) per group prior to commencing the SHIV challenge protocol. SHIV challenge 10 has been completed.
FIG. 11 . Env.BG505 binding antibody titers at time of SHIV infection in animals vaccinated with VSVΔG-Env.BG505. ELISA was conducted with Env.BG505 gp120 bound to the plate using serum samples collected from macaques at the time challenge commenced (week 48) and periodically during the challenge protocol ( FIG. 7 ). Animals 11 and 15 were infected at SHIV challenge 1 and 2, respectively. Animal 16 was infected at challenge 8, which was 19 weeks after the challenge protocol commenced. Colored arrows point to ELISA titers for animals 11, 15, and 16.
FIG. 12 . Generation of VSVΔG-Env.BG505 from DNA and summary of steps to produce a seed virus for use in vaccine manufacturing.
FIG. 13 . Preparation of VSVΔG-Env.BG505 with G pseudotype. The schematic summarizes a procedure for preparing pseudotyped VSVΔG-Env.BG505.
FIG. 14 shows that VSVΔG-Env.BG505 is cytolytic and that it forms plaques after an overnight incubation on GHOST cells.
FIG. 15 shows that three Env mutations were present in the protective VSVΔG-Env.BG505 vaccine. Adaptive mutations emerged in Env during vector rescue and propagation that increased Env-dependent replication in VeroCD4/CCR5 cells (human CD4/CCR5). The substitutions are stable and were included in vaccine vector tested in macaques. The ‘adapted Env’ gene was incorporated into a new VSVDG-Env.BG505 genomic DNA clone that allowed rescue of a recombinant virus containing these mutations.
FIGS. 16A-16B show dependence of VSVΔG-EnvG.BG505 infection on CD4 and CCR5. The virus used in this experiment contained three adaptive amino substitutions in Env.BG505: K169T, I307T, and W672R. (A) VERO or VERO-CD4/CCR5 cell lines were infected with 1 plaque-forming unit per cell (PFU/cell) of VSVΔG-Env.BG505 or a mock control. Cytopathic effect caused by VSVΔG-Env.BG505 infection is evident only VERO-CD4/CCR5 cells. (B) HOS cells expressing CD4, CCR5 or both were infected with 0.1 PFU/cell of VSVΔG-Env.BG505 or a mock control. Cytopathic effect produced by infection is only evident on cells expressing both CD4 and CCR5.
FIG. 17A-17B shows results from a maximal tolerated dose study conducted by intracranial injection in mice. Three VSVΔG-Env.BG505 vaccine preparations were analyzed: VSVΔG-Env.BG505 with a New Jersey G-pseudotype, VSVΔG-Env.BG505 with an Indiana G-pseudotype and VSVΔG-Env.BG505. No adverse events were observed following intracranial inoculation with VSVΔG vectors. (A) No substantial weight loss in animals over the 14 days apart from a small decrease at day 1. There was 100% survival in 10̂4, 10̂5 and 10̂6 pfu groups. (B) No mortality and no paralysis, limb weakness or loss of coordination was observed in any of the groups.
FIG. 18 depicts an evaluation of CD4 gene copy number in a VERO-CD4/CCR5 preclinical cell line. VERO-CD4/CCR5 cells were thawed, 3 passages were produced (P1, P2 and P3), cellular genomic DNA (gDNA) was purified and RNase treated, DNA concentrations were determined by UV spectrophotometry and diluted to a stock concentration of 100 ng/ml, genetic integrity was determined by PCR/gel electrophoresis and stability was monitored by qPCR. Stability of CD4 and CCR5 genes in the VERO-CD4/CCR5 cell line is determined. Passage to passage consistency of the VERO-CD4/CCR5 cells was monitored. Three SYBR green qPCR assays (CD4, CCR5 and a reference gene β-glucuronidase) are designed. Absolute quantification is by a standard curve method. The stability of CD4 and CD4 copy number/cell is determined by the copy ratio of CD4 to β-glucuronidase and likewise CCR5 stability.
FIGS. 19A-19E . VSV-HIV vectors evaluated in Indian rhesus macaques. (A) The VSV genome map is colored to correspond with proteins in the virus particle illustration. The 11-kb single-stranded, negative-sense, nonsegmented RNA genome encodes 5 proteins: (N) Nucleocapsid; Phosphoprotein (P); Large (L) RNA-dependent RNA polymerase subunit; (M) Matrix protein; (G) Glycoprotein. A single 3′ promoter controls mRNA synthesis, with promoter-proximal genes being transcribed more frequently. The G gene was replaced with Env.BG505 sequence in VSVΔG-Env.BG505 (B) and VSV-G6-Env.BG505 (C), with G being reintroduced at the 5′ terminus (position 6) of the VSV-G6-Env.BG505 genome. Env.BG505 encoded by both vectors was modified ( FIG. 23A ) to increase incorporation into the virus particle. (D) The surface of infected VERO or VERO-CD4/CCR5 cells was analyzed by flow cytometry using monoclonal antibodies specific for: high-manose glycans (2G12); a V3 epitope composed of polypeptide and glycan (PGT121); the CD4 binding site in native spikes (VRC01 and VRC06b) or in less compact Env species (F105 and IgGb6); and, native structures formed at the interface of spike subunits (PGT145 and PGT151). (E) Purified virus particles also were analyzed with the same antibodies using alum as a carrier for flow cytometry.
FIGS. 20A-20B . Preclinical efficacy study. (A) Macaques were vaccinated three times by applying VSVΔG-EnvG505, VSV-G6-Env.BG505, or buffered solution to both intranasal (1×10 8 pfus) and intraoral mucosal surfaces (1×10 8 pfus). Intrarectal challenge with SHIV began 5 months after the final vaccination (study week 48). The SHIV SF162p3 challenge stock was prepared in macaque PBMCs and has been used in prior studies. Consensus nucleotide sequencing conducted with the challenge virus verified that the Env gene matched Genbank Accession KF042063. Macaques with SHIV genome copies ≧200 per ml on two successive blood draws were considered positive ( FIG. 26 ) and further challenge was ended. (B) Kaplan-Meier survival curves by treatment assignment. P-values are from an exact log-rank test comparing each active treatment group to the control group.
FIGS. 21A-21D . Serum antibody analysis by Western blot. Western blot membranes were prepared using purified VSVΔG-Env.BG505 as a source of Env.BG505 and VSV polypeptides. The membranes were placed in multichannel devices to allow analysis of sera from individual animals. (A) Analysis of week-43 sera from all vaccinated animals and two controls. Labeled above the blot are the vaccine groups, animal numbers (NHP, nonhuman primate), and the SHIV challenge when infection occurred. Underlined NHP numbers indicate an animal that became infected during SHIV challenge. Polypeptide identities are labeled at the left side. Bands corresponding to Env gp41 were not clearly evident until after SHIV infection ( FIG. 30 ). (B) Sera were analyzed from week 48. An independent full-length blot is included in FIG. 30A with all control animal sera. (C) Sera was analyzed from week 62 when 5 of 10 challenges were complete. Asterisks indicate animals infected after 5 challenges. Infected Control animal 31 did not produce an Env signal probably because it had a more severe progressive infection ( FIG. 26 ) that interfered with humoral responses against Env and Gag ( FIG. 27 ). (D) Analysis of sera from week 79, which was ˜1 year after the final vaccination.
FIGS. 22A-22B . Mapping Env antibody binding regions. (A) Linear map of Env Constant (C1-C5) and Variable (V1-V5) domains. The map breaks at furin cleavage site between gp120 and gp41. The transmembrane (TM) region and cytoplasmic tail (CT) are labeled in gp41. Below the map, boundaries are shown for the Env fragments fused to human serum albumin (HSA) to generate ELISA substrates. (B) Analysis of sera using capture ELISA and the HSA fusion proteins shown in (A). HSA without a fused Env sequence was included as a negative control. Env gp120 and gp140 ELISA substrates were not fused to HSA. The data from an example experiment (absorbance at 450 nm; A450) is presented as a heat map with the scale shown at the bottom adjacent to a scale showing the SHIV challenge when infection occurred.
FIGS. 23A-23F . VSV-HIV vaccine design details. (A) Both vectors express HIV Env.BG505, which was modified to increase incorporation into the VSV particle by replacing the signal sequence, transmembrane region (TM) and cytoplasmic tail (CT) with sequence from G (serotype Indiana; IND). (B) VSVΔG-Env.BG505 particles used for vaccination were pseudotyped with G. Vaccinating with pseudotyped VSVΔG-Env.BG505 launches a more robust infection, because G binds ubiquitous cellular receptors allowing the initial round of infection to be independent of Env and the limited population of CD4+/CCR5+ cells. Pseudotyped virus was prepared by conducting the final amplification of vaccine material in VERO-CD4/CCR5 cells expressing G. (D-F) These schematics summarize how early stages of VSV vector infection progresses in macaques with pseudotyped VSVΔG-Env.BG505 (B) and VSV-G6-Env.BG505 (C). Both can use G to initiate primary infection (D), but subsequent cycles of VSVΔG-Env.BG505 infection and replication are Env-dependent while VSV-G6-Env.BG505 are G dependent. Additional information on the use of G in the vaccines is provided in FIG. 24 .
FIGS. 24A-24C . VSV G serotype exchange. Because 3 vaccinations were planned and anti-G antibodies were known to develop when using VSV vectors that express G like VSV-G6-Env ( FIG. 19C ), Applicants used a G serotype exchange strategy to minimize potential effects of anti-G immunity (A) Timeline of vaccination and SHIV challenge shows how the G composition in the vaccines was varied. (B) For VSVΔG-Env.BG505, G was exchanged simply by pseudotyping with G from serotype New Jersey (NJ) or G IND. Only two different G pseudotypes were used for the three sequential vaccinations (A), because interim ELISA data showed that transient mucosal exposure to G in the pseudotyped VSVΔG-Env.BG505 particle did not elicit substantial amounts of anti-G antibodies (data not shown). (C) For sequential vaccination with VSV-G6-Env.BG505 (B), three vectors were used that differed in their G genes. The G genes came from different vesiculoviruses including VSV serotypes NJ or IND, or Maraba virus.
FIG. 25 . VSV-HIV shedding in the oral cavity. Samples were collected at 3 days after each of the three vaccinations by swabbing the oral cavity. Samples also were collected 7 days after the first vaccination. Material collected on the swabs was purified using procedures described in the Methods for detecting SHIV genomes in plasma after which qPCR was performed with an amplicon specific for the N gene. The lower limit of measurement was 50 genome copies per reaction. Low quantities of VSVΔG-EnvG.BG505 genomes were detected at 3 days following the first vaccination in 4 animals and in 3 macaques after the third vaccination. VSV-G6-Env.BG505 genomes were detected in swabs from 8 animals in greater quantities after the first vaccination and in 4 macaques following the third vaccination. These results indicated that VSVΔG-Env.BG505 shedding into the oral cavity was minimal to undetectable, while the quantity of VSV-G6-Env.BG505 genomes indicated that some virus shedding occurred although it remains to be determined whether live virus was present.
FIG. 26 . SHIV infection and virus loads. Blood was collected at one and two weeks following each challenge to assess virus loads as described in the Methods. The plots show SHIV genome copies per ml of plasma as measured by RT-qPCR using a SIV Gag-specific amplicon. Animals with ≧200 copies on two successive blood draws were considered positive after which challenge was stopped. Animal numbers are shown to the right of the plots, and those positive for the Mamu-A*01 or Mamu-A*02 MHC alleles are indicated. Each group had two animals that were positive for Mamu-A*01 and two positive Mamu-A*02, which have been associated with control of disease progression. No macaques were included in the study with Mamu-B*17 or Mamu-B*08 alleles associated with strong replication control. Two animals in the Control group (indicated with X) experienced rapid disease progression and were euthanized before the end of the study.
FIGS. 27A-27C . Analysis of anti-Gag response to SHIV infection by Western blotting. (A) SHIV challenge timeline and labeling key for the blots below. (B-C) Gag-specific serum antibodies were detected by reactivity with recombinant SIV Gag (SIVmac239, p55 Gag; Protein Sciences Corp.) on Western blot membranes. Week-62 serum (B) was collected after completing the first 5 challenges and week-79 serum (C) was collected two months after the 10th challenge. Animal numbers are indicated above each lane, and in (B), an asterisk indicates that macaques were infected by the fifth challenge. Two infected animals in the control group (31 and 40) did not have strong anti-Gag or anti-Env ( FIG. 30C ) antibody responses, which was due to rapid disease progression ( FIG. 26 ) inhibiting development of antibodies.
FIGS. 28A-28B . More detailed presentation of the SHIV infection timeline. (A) The Table supplements the survival curve shown in FIG. 20B and the antibody analysis in 3B by provides the timing of SHIV infection for each animal. (B) Boxplots showing ELISA titers during vaccination and challenge phases. The boxplots highlight the low titers in animals 11, 15, and 16 in the VSVΔG-Env.BG505 group prior to SHIV infection. Boxes show median and quartiles with whiskers extending at most 1.5 times the interquartile range.
FIG. 29 . CD4 and CD8 T cell frequencies in peripheral blood. PBMCs harvested two weeks after the third vaccination (week 31) were stimulated with peptides representing Env.BG505 gp120, gp41, or VSV N after which intracellular cytokine staining and flow cytometry was conducted to quantify CD4 and CD8 T cells. Overall, the Env-specific T cell frequencies in peripheral blood were low (measurable limit set at 0.05%). In the VSV-G6-Env.BG505 group 5 of 10 animals were positive for gp120-specific CD4 T cells secreting IFNγ. VSV N-specific CD8 T cells also were detected secreting IFNγ in 9 of 10 macaques and TNFα in 4 or 10 animals. Notably, the frequency of T cells in peripheral blood specific for Env or N were below measurable limits in the group vaccinated with VSVΔG-Env.BG505.
FIGS. 30A-30C . Additional characterization of serum antibodies by Western blot. Assays were performed as in FIG. 21 . (A) An independent week-48 Western blot, like the one in FIG. 21B , is shown with all control animals included. The full-length blot also shows reactivity with VSV polypeptides as described in FIG. 21A . Sera from control animals lacked significant VSV and Env signals as expected, except for occasional detection of bands that migrated at positions consistent with VSV M and P. (B) A Western blot performed with sera collected at study week 16, which was 12 weeks after the second vaccination. The result showed that the Env signal was detectable at this earlier time even though the ELISA titers were considerably lower in the VSVΔG-Env.BG505 group after the second vaccination. (C) An independent week-79 Western blot similar to the one in FIG. 21D . The full length blot shows that serum from infected macaques was able to detect gp41. Most control macaques also developed antibodies that bound gp41 except for two animals that had had progressive infections (macaques 31 and 40; FIG. 26 ) and uninfected animal 32. Animal 31 was euthanized prior to this time point.
FIG. 31 . Cross clade Env binding detected with Western blot. A Western blot assay was performed using three different VSVΔG-Env.BG505 chimeras as the source of proteins on the blot. These included clade A.BG505 (different blot than in FIG. 4B ), B.SF162.p3, and C.CH505 (week 100). The assay was performed as described in FIG. 21 using sera from the VSVΔG-Env.BG505 group (week 48). Animal numbers are at the top of the blot. Underlined animals were not protected during SHIV challenge.
FIG. 32 . Analysis of serum antibody binding to different Env regions by Western blotting. Sera from week 48 was analyzed as described in FIG. 21 except that recombinant gp120, gp140, and HSA fusion proteins ( FIG. 22A ) were used as substrates. The positive control lane (+) included anti-HIS antibody.
FIGS. 33A-33I . Sequence annotation of VERO-hCD4/CCR5 gene. A restriction map of the Vert construct shows restriction enzymes cutting a maximum of two times, using RELibrary as a restriction enzyme library. FIGS. 33A-33I disclose the top nucleic acid sequence as SEQ ID NO: 7 and the coded protein sequence as SEQ ID NO: 8.
FIG. 34 . Gene design: VERO-CD4/CCR5 Cell Line(VERT). VERO-hCD4/CCR5: Transgenic Vero cells expression human CD4 and CCR5 receptors. sVERT3: Transgenic Vero cells expression simian CD4 and CCR5 receptors.
FIG. 35 . VERO-hCD4/CCR5 clone 4F11 resembles the Vero cell.
FIG. 36 . VERO-hCD4/CCR5 cytopathic effect when infected by VSV chimera.
FIG. 37 . VERO-hCD4/CCR5 maintains infectivity over 20 passages.
FIG. 38 . VERO-hCD4/CCR5 maintains the receptor expression over 20 passages.



DETAILED DESCRIPTION
The terms “protein”, “peptide”, “polypeptide”, and “amino acid sequence” are used interchangeably herein to refer to polymers of amino acid residues of any length. The polymer may be linear or branched, it may comprise modified amino acids or amino acid analogs, and it may be interrupted by chemical moieties other than amino acids. The terms also encompass an amino acid polymer that has been modified naturally or by intervention; for example disulfide bond formation, glycosylation, lipidation, acetylation, phosphorylation, or any other manipulation or modification, such as conjugation with a labeling or bioactive component.
As used herein, the terms “antigen” or “immunogen” are used interchangeably to refer to a substance, typically a protein, which is capable of inducing an immune response in a subject. The term also refers to proteins that are immunologically active in the sense that once administered to a subject (either directly or by administering to the subject a nucleotide sequence or vector that encodes the protein) is able to evoke an immune response of the humoral and/or cellular type directed against that protein.
The term “antibody” includes intact molecules as well as fragments thereof, such as Fab, F(ab′) 2 , Fv and scFv which are capable of binding the epitope determinant. These antibody fragments retain some ability to selectively bind with its antigen or receptor and include, for example:
(i) Fab, the fragment which contains a monovalent antigen-binding fragment of an antibody molecule can be produced by digestion of whole antibody with the enzyme papain to yield an intact light chain and a portion of one heavy chain; (ii) Fab′, the fragment of an antibody molecule can be obtained by treating whole antibody with pepsin, followed by reduction, to yield an intact light chain and a portion of the 20 heavy chain; two Fab′ fragments are obtained per antibody molecule; (iii) F(ab′) 2 , the fragment of the antibody that can be obtained by treating whole antibody with the enzyme pepsin without subsequent reduction; F(ab′) 2 is a dimer of two Fab′ fragments held together by two disulfide bonds; (iv) scFv, including a genetically engineered fragment containing the variable region of a heavy and a light chain as a fused single chain molecule.

General methods of making these fragments are known in the art. (See for example, Harlow and Lane, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, New York (1988), which is incorporated herein by reference).
It should be understood that the proteins, including the proteins of the invention may differ from the exact sequences illustrated and described herein. Thus, the invention contemplates deletions, additions and substitutions to the sequences shown, so long as the sequences function in accordance with the methods of the invention. In this regard, particularly preferred substitutions will generally be conservative in nature, i.e., those substitutions that take place within a family of amino acids. For example, amino acids are generally divided into four families: (1) acidic—aspartate and glutamate; (2) basic—lysine, arginine, histidine; (3) non-polar—alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan; and (4) uncharged polar—glycine, asparagine, glutamine, cysteine, serine threonine, tyrosine. Phenylalanine, tryptophan, and tyrosine are sometimes classified as aromatic amino acids. It is reasonably predictable that an isolated replacement of leucine with isoleucine or valine, or vice versa; an aspartate with a glutamate or vice versa; a threonine with a serine or vice versa; or a similar conservative replacement of an amino acid with a structurally related amino acid, will not have a major effect on the biological activity. Proteins having substantially the same amino acid sequence as the sequences illustrated and described but possessing minor amino acid substitutions that do not substantially affect the immunogenicity of the protein are, therefore, within the scope of the invention.
As used herein the terms “nucleotide sequences” and “nucleic acid sequences” refer to deoxyribonucleic acid (DNA) or ribonucleic acid (RNA) sequences, including, without limitation, messenger RNA (mRNA), DNA/RNA hybrids, or synthetic nucleic acids. The nucleic acid can be single-stranded, or partially or completely double-stranded (duplex). Duplex nucleic acids can be homoduplex or heteroduplex.
As used herein the term “transgene” may be used to refer to “recombinant” nucleotide sequences that may be derived from any of the nucleotide sequences encoding the proteins of the present invention. The term “recombinant” means a nucleotide sequence that has been manipulated “by man” and which does not occur in nature, or is linked to another nucleotide sequence or found in a different arrangement in nature. It is understood that manipulated “by man” means manipulated by some artificial means, including by use of machines, codon optimization, restriction enzymes, etc.
For example, in one embodiment the nucleotide sequences may be mutated such that the activity of the encoded proteins in vivo is abrogated. For example, each of the Gag, Pol, Env, Nef, RT, and Int sequences of the invention may be altered in these ways.
As regards codon optimization, the nucleic acid molecules of the invention have a nucleotide sequence that encodes the antigens of the invention and can be designed to employ codons that are used in the genes of the subject in which the antigen is to be produced. Many viruses, including HIV and other lentiviruses, use a large number of rare codons and, by altering these codons to correspond to codons commonly used in the desired subject, enhanced expression of the antigens can be achieved. In a preferred embodiment, the codons used are “humanized” codons, i.e., the codons are those that appear frequently in highly expressed human genes (Andre et al., J. Virol. 72:1497-1503, 1998) instead of those codons that are frequently used by HIV. Such codon usage provides for efficient expression of the transgenic HIV proteins in human cells. Any suitable method of codon optimization may be used. Such methods, and the selection of such methods, are well known to those of skill in the art. In addition, there are several companies that will optimize codons of sequences, such as Geneart (geneart.com). Thus, the nucleotide sequences of the invention can readily be codon optimized.
Advantageously, Applicants codon optimize the Env gene so it has the codon bias that is characteristic of VSV. This also results in a relatively low Guanine+Cytosine content of about 40-45%. See, e.g., Rabinovich et al., PLoS One. 2014 Sep. 12; 9(9):e106597. doi: 10.1371/journal.pone.0106597. eCollection 2014.
The invention further encompasses nucleotide sequences encoding functionally and/or antigenically equivalent variants and derivatives of the antigens of the invention and functionally equivalent fragments thereof. These functionally equivalent variants, derivatives, and fragments display the ability to retain antigenic activity. For instance, changes in a DNA sequence that do not change the encoded amino acid sequence, as well as those that result in conservative substitutions of amino acid residues, one or a few amino acid deletions or additions, and substitution of amino acid residues by amino acid analogs are those which will not significantly affect properties of the encoded polypeptide. Conservative amino acid substitutions are glycine/alanine; valine/isoleucine/leucine; asparagine/glutamine; aspartic acid/glutamic acid; serine/threonine/methionine; lysine/arginine; and phenylalanine/tyrosine/tryptophan. In one embodiment, the variants have at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 86%, at least 87%, at least 88%, at least 89%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98% or at least 99% homology or identity to the antigen, epitope, immunogen, peptide or polypeptide of interest.
For the purposes of the present invention, sequence identity or homology is determined by comparing the sequences when aligned so as to maximize overlap and identity while minimizing sequence gaps. In particular, sequence identity may be determined using any of a number of mathematical algorithms. A nonlimiting example of a mathematical algorithm used for comparison of two sequences is the algorithm of Karlin & Altschul, Proc. Natl. Acad. Sci. USA 1990; 87: 2264-2268, modified as in Karlin & Altschul, Proc. Natl. Acad. Sci. USA 1993; 90: 5873-5877.
Another example of a mathematical algorithm used for comparison of sequences is the algorithm of Myers & Miller, CABIOS 1988; 4: 11-17. Such an algorithm is incorporated into the ALIGN program (version 2.0) which is part of the GCG sequence alignment software package. When utilizing the ALIGN program for comparing amino acid sequences, a PAM120 weight residue table, a gap length penalty of 12, and a gap penalty of 4 can be used. Yet another useful algorithm for identifying regions of local sequence similarity and alignment is the FASTA algorithm as described in Pearson & Lipman, Proc. Natl. Acad. Sci. USA 1988; 85: 2444-2448.
Advantageous for use according to the present invention is the WU-BLAST (Washington University BLAST) version 2.0 software. WU-BLAST version 2.0 executable programs for several UNIX platforms can be downloaded from ftp://blast.wustl.edu/blast/executables. This program is based on WU-BLAST version 1.4, which in turn is based on the public domain NCBI-BLAST version 1.4 (Altschul & Gish, 1996, Local alignment statistics, Doolittle ed., Methods in Enzymology 266: 460-480; Altschul et al., Journal of Molecular Biology 1990; 215: 403-410; Gish & States, 1993; Nature Genetics 3: 266-272; Karlin & Altschul, 1993; Proc. Natl. Acad. Sci. USA 90: 5873-5877; all of which are incorporated by reference herein).
The various recombinant nucleotide sequences and proteins of the invention are made using standard recombinant DNA and cloning techniques. Such techniques are well known to those of skill in the art. See for example, “Molecular Cloning: A Laboratory Manual”, second edition (Sambrook et al. 1989).
The nucleotide sequences of the present invention may be inserted into “vectors.” The term “vector” is widely used and understood by those of skill in the art, and as used herein the term “vector” is used consistent with its meaning to those of skill in the art. For example, the term “vector” is commonly used by those skilled in the art to refer to a vehicle that allows or facilitates the transfer of nucleic acid molecules from one environment to another or that allows or facilitates the manipulation of a nucleic acid molecule.
Any vector that allows expression of the proteins of the present invention may be used in accordance with the present invention. In certain embodiments, the antigens and/or antibodies of the present invention may be used in vitro (such as using cell-free expression systems) and/or in cultured cells grown in vitro in order to produce the encoded antigens, such as HIV-antigens, and/or antibodies which may then be used for various applications such as in the production of proteinaceous vaccines. For such applications, any vector that allows expression of the antigens and/or antibodies in vitro and/or in cultured cells may be used.
For applications where it is desired that the proteins be expressed in vivo, for example when the transgenes of the invention are used in DNA or DNA-containing vaccines, any vector that allows for the expression of the proteins of the present invention and is safe for use in vivo may be used. In preferred embodiments the vectors used are safe for use in humans, mammals and/or laboratory animals.
For the proteins of the present invention to be expressed, the protein coding sequence should be “operably linked” to regulatory or nucleic acid control sequences that direct transcription and translation of the protein. As used herein, a coding sequence and a nucleic acid control sequence or promoter are said to be “operably linked” when they are covalently linked in such a way as to place the expression or transcription and/or translation of the coding sequence under the influence or control of the nucleic acid control sequence. The “nucleic acid control sequence” can be any nucleic acid element, such as, but not limited to promoters, enhancers, IRES, introns, and other elements described herein that direct the expression of a nucleic acid sequence or coding sequence that is operably linked thereto. The term “promoter” will be used herein to refer to a group of transcriptional control modules that are clustered around the initiation site for RNA polymerase II and that when operationally linked to the protein coding sequences of the invention lead to the expression of the encoded protein. The expression of the transgenes of the present invention can be under the control of a constitutive promoter or of an inducible promoter, which initiates transcription only when exposed to some particular external stimulus, such as, without limitation, antibiotics such as tetracycline, hormones such as ecdysone, or heavy metals. The promoter can also be specific to a particular cell-type, tissue or organ. Many suitable promoters and enhancers are known in the art, and any such suitable promoter or enhancer may be used for expression of the transgenes of the invention. For example, suitable promoters and/or enhancers can be selected from the Eukaryotic Promoter Database (EPDB).
The present invention relates to a Vero cell line transformed with and expressing a cluster of differentiation 4 (CD4) receptor and a C—C chemokine receptor type 5 (CCR5 receptor).
The Vero cell lineage was isolated from kidney epithelial cells extracted from an African green monkey ( Chlorocebus sp.; formerly called Cercopithecus aethiops , this group of monkeys has been split into several different species). The genome sequence was determined by Osada N, Kohara A, Yamaji T, Hirayama N, Kasai F, Sekizuka T, Kuroda M, Hanada K (2014). “The genome landscape of the African green monkey kidney-derived Vero cell line”. DNA Research. 21: 673-83. doi:10.1093/dnares/dsu029. The ATCC supplies various different Vero cells under catalog numbers CCL-81, CCL-81.2, CRL-1586 and CRL-1587. Vero cells support the growth of pathogens such as: pneumoviruses, such as RSV-A and RSV-B; human metapneumoviruses (HMPV); morbilliviruses, such as measles virus; paramyxoviruses, such as mumps virus and parainfluenza virus; rubellavirus; human and avian coronaviruses; picornaviruses, such as entroviruses, echoviruses and coxsackie viruses, and porcine SVDV and Teschen-Talfan virus; mammalian and avian reoviruses; herpesviruses, such as HSV-1 and HSV-2; simian and human adenoviruses; varicella zoster virus (VZV); polyomaviruses, such as JC, BK and SV-40; bimaviruses, such as gumborovirus; porcine circoviruses; canine parvovirus; and Chlamydia.
CD4 is a co-receptor that assists the T cell receptor (TCR) in communicating with an antigen-presenting cell. Using its intracellular domain, CD4 amplifies the signal generated by the TCR by recruiting an enzyme, the tyrosine kinase Lck, which is essential for activating many molecular components of the signaling cascade of an activated T cell. Various types of T helper cells are thereby produced. CD4 also interacts directly with MHC class II molecules on the surface of the antigen-presenting cell using its extracellular domain. The extracellular domain adopts an immunoglobulin-like beta-sandwich with seven strands in 2 beta sheets, in a Greek key topology.
During antigen presentation, both the TCR complex and CD4 are recruited to bind to different regions of the MHCII molecule (α1/β1 and β2, respectively). Close proximity between the TCR complex and CD4 in this situation means the Lck kinase bound to the cytoplasmic tail of CD4 is able to tyrosine-phosphorylate the Immunoreceptor tyrosine activation motifs (ITAM) present on the cytoplasmic domains of CD3. Phosphorylated ITAM motifs on CD3 recruits and activates SH2 domain-containing protein tyrosine kinases (PTK) such as Zap70 to further mediate downstream signal transduction via tyrosine phosphorylation, leading to transcription factor activation including NF-κB and consequent T cell activation.
Human CD4 amino acid sequences may be found, for example, in Crise et al., J. Virol. 64:5585-5593(1990); Lusso et al., Proc. Natl. Acad. Sci. U.S.A. 91:3872-3876(1994); Sharma et al., Biochemistry 44:16192-16202(2005); Lindwasser et al., Curr. Mol. Med. 7:171-184(2007) and Kwong et al., Nature 393:648-659(1998).
Simian CD4 amino acid sequences may be found, for example, in Fomsgaard et al., Eur J Immunol. 1992 November; 22(11):2973-81.
C—C chemokine receptor type 5, also known as CCR5 or CD195, is a protein on the surface of white blood cells that is involved in the immune system as it acts as a receptor for chemokines. This is the process by which T cells are attracted to specific tissue and organ targets. Many forms of HIV, the virus that causes AIDS, initially use CCR5 to enter and infect host cells.
Human CD4 amino acid sequences may be found, for example, in Rizzuto et al., Science 280:1949-1953(1998) and Schnur et al., J. MOl. Biol. 410:778-797(2011).
Simian CD4 amino acid sequences may be found, for example, in Kunstman et al., J Virol. 2003 November; 77(22): 12310-12318.
In an advantageous embodiment, HIV-1 utilizes CD4 to gain entry into host T-cells and achieves this through viral envelope protein gp120. The binding to CD4 creates a shift in the conformation of gp120 allowing HIV-1 to bind to a CCR5 or CXCR4 co-receptor expressed on the host cell. Following a structural change in viral protein gp41, HIV inserts a fusion peptide into the host cell that allows the outer membrane of the virus to fuse with the cell membrane.
The present invention relates to a recombinant vesicular stomatitis virus (VSV) vector expressing a foreign epitope. Advantageously, the epitope is an HIV epitope. Any HIV epitope may be expressed in a VSV vector. Advantageously, the HIV epitope is an HIV antigen, HIV epitope or an HIV immunogen, such as, but not limited to, the HIV antigens, HIV epitopes or HIV immunogens of U.S. Pat. Nos. 7,341,731; 7,335,364; 7,329,807; 7,323,553; 7,320,859; 7,311,920; 7,306,798; 7,285,646; 7,285,289; 7,285,271; 7,282,364; 7,273,695; 7,270,997; 7,262,270; 7,244,819; 7,244,575; 7,232,567; 7,232,566; 7,223,844; 7,223,739; 7,223,534; 7,223,368; 7,220,554; 7,214,530; 7,211,659; 7,211,432; 7,205,159; 7,198,934; 7,195,768; 7,192,555; 7,189,826; 7,189,522; 7,186,507; 7,179,645; 7,175,843; 7,172,761; 7,169,550; 7,157,083; 7,153,509; 7,147,862; 7,141,550; 7,129,219; 7,122,188; 7,118,859; 7,118,855; 7,118,751; 7,118,742; 7,105,655; 7,101,552; 7,097,971 7,097,842; 7,094,405; 7,091,049; 7,090,648; 7,087,377; 7,083,787; 7,070,787; 7,070,781; 7,060,273; 7,056,521; 7,056,519; 7,049,136; 7,048,929; 7,033,593; 7,030,094; 7,022,326; 7,009,037; 7,008,622; 7,001,759; 6,997,863; 6,995,008; 6,979,535; 6,974,574; 6,972,126; 6,969,609; 6,964,769; 6,964,762; 6,958,158; 6,956,059; 6,953,689; 6,951,648; 6,946,075; 6,927,031; 6,919,319; 6,919,318; 6,919,077; 6,913,752; 6,911,315; 6,908,617; 6,908,612; 6,902,743; 6,900,010; 6,893,869; 6,884,785; 6,884,435; 6,875,435; 6,867,005; 6,861,234; 6,855,539; 6,841,381 6,841,345; 6,838,477; 6,821,955; 6,818,392; 6,818,222; 6,815,217; 6,815,201; 6,812,026; 6,812,025; 6,812,024; 6,808,923; 6,806,055; 6,803,231; 6,800,613; 6,800,288; 6,797,811; 6,780,967; 6,780,598; 6,773,920; 6,764,682; 6,761,893; 6,753,015; 6,750,005; 6,737,239; 6,737,067; 6,730,304; 6,720,310; 6,716,823; 6,713,301; 6,713,070; 6,706,859; 6,699,722; 6,699,656; 6,696,291; 6,692,745; 6,670,181; 6,670,115; 6,664,406; 6,657,055; 6,657,050; 6,656,471; 6,653,066; 6,649,409; 6,649,372; 6,645,732; 6,641,816; 6,635,469; 6,613,530; 6,605,427; 6,602,709 6,602,705; 6,600,023; 6,596,477; 6,596,172; 6,593,103; 6,593,079; 6,579,673; 6,576,758; 6,573,245; 6,573,040; 6,569,418; 6,569,340; 6,562,800; 6,558,961; 6,551,828; 6,551,824; 6,548,275; 6,544,780; 6,544,752; 6,544,728; 6,534,482; 6,534,312; 6,534,064; 6,531,572; 6,531,313; 6,525,179; 6,525,028; 6,524,582; 6,521,449; 6,518,030; 6,518,015; 6,514,691; 6,514,503; 6,511,845; 6,511,812; 6,511,801; 6,509,313; 6,506,384; 6,503,882; 6,495,676; 6,495,526; 6,495,347; 6,492,123; 6,489,131; 6,489,129; 6,482,614; 6,479,286; 6,479,284; 6,465,634; 6,461,615 6,458,560; 6,458,527; 6,458,370; 6,451,601; 6,451,592; 6,451,323; 6,436,407; 6,432,633; 6,428,970; 6,428,952; 6,428,790; 6,420,139; 6,416,997; 6,410,318; 6,410,028; 6,410,014; 6,407,221; 6,406,710; 6,403,092; 6,399,295; 6,392,013; 6,391,657; 6,384,198; 6,380,170; 6,376,170; 6,372,426; 6,365,187; 6,358,739; 6,355,248; 6,355,247; 6,348,450; 6,342,372; 6,342,228; 6,338,952; 6,337,179; 6,335,183; 6,335,017; 6,331,404; 6,329,202; 6,329,173; 6,328,976; 6,322,964; 6,319,666; 6,319,665; 6,319,500; 6,319,494; 6,316,205; 6,316,003; 6,309,633; 6,306,625 6,296,807; 6,294,322; 6,291,239; 6,291,157; 6,287,568; 6,284,456; 6,284,194; 6,274,337; 6,270,956; 6,270,769; 6,268,484; 6,265,562; 6,265,149; 6,262,029; 6,261,762; 6,261,571; 6,261,569; 6,258,599; 6,258,358; 6,248,332; 6,245,331; 6,242,461; 6,241,986; 6,235,526; 6,235,466; 6,232,120; 6,228,361; 6,221,579; 6,214,862; 6,214,804; 6,210,963; 6,210,873; 6,207,185; 6,203,974; 6,197,755; 6,197,531; 6,197,496; 6,194,142; 6,190,871; 6,190,666; 6,168,923; 6,156,302; 6,153,408; 6,153,393; 6,153,392; 6,153,378; 6,153,377; 6,146,635; 6,146,614; 6,143,876 6,140,059; 6,140,043; 6,139,746; 6,132,992; 6,124,306; 6,124,132; 6,121,006; 6,120,990; 6,114,507; 6,114,143; 6,110,466; 6,107,020; 6,103,521; 6,100,234; 6,099,848; 6,099,847; 6,096,291; 6,093,405; 6,090,392; 6,087,476; 6,083,903; 6,080,846; 6,080,725; 6,074,650; 6,074,646; 6,070,126; 6,063,905; 6,063,564; 6,060,256; 6,060,064; 6,048,530; 6,045,788; 6,043,347; 6,043,248; 6,042,831; 6,037,165; 6,033,672; 6,030,772; 6,030,770; 6,030,618; 6,025,141; 6,025,125; 6,020,468; 6,019,979; 6,017,543; 6,017,537; 6,015,694; 6,015,661; 6,013,484; 6,013,432 6,007,838; 6,004,811; 6,004,807; 6,004,763; 5,998,132; 5,993,819; 5,989,806; 5,985,926; 5,985,641; 5,985,545; 5,981,537; 5,981,505; 5,981,170; 5,976,551; 5,972,339; 5,965,371; 5,962,428; 5,962,318; 5,961,979; 5,961,970; 5,958,765; 5,958,422; 5,955,647; 5,955,342; 5,951,986; 5,951,975; 5,942,237; 5,939,277; 5,939,074; 5,935,580; 5,928,930; 5,928,913; 5,928,644; 5,928,642; 5,925,513; 5,922,550; 5,922,325; 5,919,458; 5,916,806; 5,916,563; 5,914,395; 5,914,109; 5,912,338; 5,912,176; 5,912,170; 5,906,936; 5,895,650; 5,891,623; 5,888,726; 5,885,580 5,885,578; 5,879,685; 5,876,731; 5,876,716; 5,874,226; 5,872,012; 5,871,747; 5,869,058; 5,866,694; 5,866,341; 5,866,320; 5,866,319; 5,866,137; 5,861,290; 5,858,740; 5,858,647; 5,858,646; 5,858,369; 5,858,368; 5,858,366; 5,856,185; 5,854,400; 5,853,736; 5,853,725; 5,853,724; 5,852,186; 5,851,829; 5,851,529; 5,849,475; 5,849,288; 5,843,728; 5,843,723; 5,843,640; 5,843,635; 5,840,480; 5,837,510; 5,837,250; 5,837,242; 5,834,599; 5,834,441; 5,834,429; 5,834,256; 5,830,876; 5,830,641; 5,830,475; 5,830,458; 5,830,457; 5,827,749; 5,827,723; 5,824,497 5,824,304; 5,821,047; 5,817,767; 5,817,754; 5,817,637; 5,817,470; 5,817,318; 5,814,482; 5,807,707; 5,804,604; 5,804,371; 5,800,822; 5,795,955; 5,795,743; 5,795,572; 5,789,388; 5,780,279; 5,780,038; 5,776,703; 5,773,260; 5,770,572; 5,766,844; 5,766,842; 5,766,625; 5,763,574; 5,763,190; 5,762,965; 5,759,769; 5,756,666; 5,753,258; 5,750,373; 5,747,641; 5,747,526; 5,747,028; 5,736,320; 5,736,146; 5,733,760; 5,731,189; 5,728,385; 5,721,095; 5,716,826; 5,716,637; 5,716,613; 5,714,374; 5,709,879; 5,709,860; 5,709,843; 5,705,331; 5,703,057; 5,702,707 5,698,178; 5,688,914; 5,686,078; 5,681,831; 5,679,784; 5,674,984; 5,672,472; 5,667,964; 5,667,783; 5,665,536; 5,665,355; 5,660,990; 5,658,745; 5,658,569; 5,643,756; 5,641,624; 5,639,854; 5,639,598; 5,637,677; 5,637,455; 5,633,234; 5,629,153; 5,627,025; 5,622,705; 5,614,413; 5,610,035; 5,607,831; 5,606,026; 5,601,819; 5,597,688; 5,593,972; 5,591,829; 5,591,823; 5,589,466; 5,587,285; 5,585,254; 5,585,250; 5,580,773; 5,580,739; 5,580,563; 5,573,916; 5,571,667; 5,569,468; 5,558,865; 5,556,745; 5,550,052; 5,543,328; 5,541,100; 5,541,057; 5,534,406 5,529,765; 5,523,232; 5,516,895; 5,514,541; 5,510,264; 5,500,161; 5,480,967; 5,480,966; 5,470,701; 5,468,606; 5,462,852; 5,459,127; 5,449,601; 5,447,838; 5,447,837; 5,439,809; 5,439,792; 5,418,136; 5,399,501; 5,397,695; 5,391,479; 5,384,240; 5,374,519; 5,374,518; 5,374,516; 5,364,933; 5,359,046; 5,356,772; 5,354,654; 5,344,755; 5,335,673; 5,332,567; 5,320,940; 5,317,009; 5,312,902; 5,304,466; 5,296,347; 5,286,852, 5,268,265; 5,264,356; 5,264,342; 5,260,308; 5,256,767; 5,256,561; 5,252,556; 5,230,998; 5,230,887; 5,227,159; 5,225,347; 5,221,610, 5,217,861; 5,208,321; 5,206,136; 5,198,346; 5,185,147; 5,178,865; 5,173,400; 5,173,399; 5,166,050; 5,156,951, 5,135,864; 5,122,446; 5,120,662; 5,103,836; 5,100,777; 5,100,662; 5,093,230; 5,077,284; 5,070,010; 5,068,174; 5,066,782; 5,055,391; 5,043,262; 5,039,604; 5,039,522; 5,030,718; 5,030,555; 5,030,449; 5,019,387; 5,013,556; 5,008,183; 5,004,697; 4,997,772; 4,983,529; 4,983,387; 4,965,069; 4,945,082; 4,921,787; 4,918,166; 4,900,548; 4,888,290; 4,886,742; 4,885,235; 4,870,003; 4,869,903; 4,861,707; 4,853,326; 4,839,288; 4,833,072 and 4,795,739.
The vector of the present invention advantageously encodes for an Env.BG505 immunogen which may be encoded by a VSVΔG-Env.BG505 vaccine. The immunogen advantageously has the sequence as provided in SEQ ID NO: 2.
In another embodiment, the vector of the present invention may comprise a sequence of a VSVΔG-Env.BG505 genomic clone. The genomic clone advantageously has the sequence as provided as SEQ ID NO: 1.
Advantageously, the HIV epitope may be an Env precursor or gp160 epitope or immunogen. The Env precursor or gp160 epitope may be recognized by antibodies PG9, PG16, 2G12, b12, 15 2F5, 4E10, Z13, or other broad potent neutralizing antibodies.
Adaptive mutations emerged in Env during vector rescue and propagation that increased Env-dependent replication in VeroCD4/CCR5 cells (human CD4/CCR5) (see, e.g., FIG. 15 ). The substitutions are stable and included in vaccine vector tested in macaques. The ‘adapted virus’ is advanced as a genomic DNA clone containing these coding changes and has been show to support rescue of recombinant virus. Therefore, the present invention also encompasses mutations of env that may increase Env-dependent replication and/or contribute to immunogenicity. The Env-VSV G hybrid (EnvG) mutations may include mutations of the lysine at AA position 169, the isoleucine at AA position 307 and/or the tryptophan at AA position 672. In an especially advantageous embodiment, the mutations are K169T, I307T and/or W672R. Other env mutations may be at P493, M343, K168, E168, Q440 and/or L494. In an advantageous embodiment, the mutations may be M343T, K168E, E168K, E164G, Q440R and/or L494F. see, e.g., Hoffenberg et al., J. Virol. May 2013 vol. 87 no. 10 5372-5383 for Env sequences and alignments.
In another embodiment, HIV, or immunogenic fragments thereof, may be utilized as the HIV epitope. For example, the HIV nucleotides of U.S. Pat. Nos. 7,393,949, 7,374,877 7,306,901, 7,303,754, 7,173,014, 7,122,180, 7,078,516, 7,022,814, 6,974,866, 6,958,211, 6,949,337, 6,946,254, 6,896,900, 6,887,977, 6,870,045, 6,803,187, 6,794,129, 6,773,915, 6,768,004, 6,706,268, 6,696,291, 6,692,955, 6,656,706, 6,649,409, 6,627,442, 6,610,476, 6,602,705, 6,582,920, 6,557,296, 6,531,587, 6,531,137, 6,500,623, 6,448,078, 6,429,306, 6,420,545, 6,410,013, 6,407,077, 6,395,891, 6,355,789, 6,335,158, 6,323,185, 6,316,183, 6,303,293, 6,300,056, 6,277,561, 6,270,975, 6,261,564, 6,225,045, 6,222,024, 6,194,391, 6,194,142, 6,162,631, 6,114,167, 6,114,109, 6,090,392, 6,060,587, 6,057,102, 6,054,565, 6,043,081, 6,037,165, 6,034,233, 6,033,902, 6,030,769, 6,020,123, 6,015,661, 6,010,895, 6,001,555, 5,985,661, 5,980,900, 5,972,596, 5,939,538, 5,912,338, 5,869,339, 5,866,701, 5,866,694, 5,866,320, 5,866,137, 5,864,027, 5,861,242, 5,858,785, 5,858,651, 5,849,475, 5,843,638, 5,840,480, 5,821,046, 5,801,056, 5,786,177, 5,786,145, 5,773,247, 5,770,703, 5,756,674, 5,741,706, 5,705,612, 5,693,752, 5,688,637, 5,688,511, 5,684,147, 5,665,577, 5,585,263, 5,578,715, 5,571,712, 5,567,603, 5,554,528, 5,545,726, 5,527,895, 5,527,894, 5,223,423, 5,204,259, 5,144,019, 5,051,496 and 4,942,122 are useful for the present invention.
Any epitope recognized by an anti-HIV antibody may be used in the present invention. For example, the anti-HIV antibodies of U.S. Pat. Nos. 6,949,337, 6,900,010, 6,821,744, 6,768,004, 6,613,743, 6,534,312, 6,511,830, 6,489,131, 6,242,197, 6,114,143, 6,074,646, 6,063,564, 6,060,254, 5,919,457, 5,916,806, 5,871,732, 5,824,304, 5,773,247, 5,736,320, 5,637,455, 5,587,285, 5,514,541, 5,317,009, 4,983,529, 4,886,742, 4,870,003 and 4,795,739 are useful for the present invention. Furthermore, monoclonal anti-HIV antibodies of U.S. Pat. Nos. 7,074,556, 7,074,554, 7,070,787, 7,060,273, 7,045,130, 7,033,593, RE39,057, 7,008,622, 6,984,721, 6,972,126, 6,949,337, 6,946,465, 6,919,077, 6,916,475, 6,911,315, 6,905,680, 6,900,010, 6,825,217, 6,824,975, 6,818,392, 6,815,201, 6,812,026, 6,812,024, 6,797,811, 6,768,004, 6,703,019, 6,689,118, 6,657,050, 6,608,179, 6,600,023, 6,596,497, 6,589,748, 6,569,143, 6,548,275, 6,525,179, 6,524,582, 6,506,384, 6,498,006, 6,489,131, 6,465,173, 6,461,612, 6,458,933, 6,432,633, 6,410,318, 6,406,701, 6,395,275, 6,391,657, 6,391,635, 6,384,198, 6,376,170, 6,372,217, 6,344,545, 6,337,181, 6,329,202, 6,319,665, 6,319,500, 6,316,003, 6,312,931, 6,309,880, 6,296,807, 6,291,239, 6,261,558, 6,248,514, 6,245,331, 6,242,197, 6,241,986, 6,228,361, 6,221,580, 6,190,871, 6,177,253, 6,146,635, 6,146,627, 6,146,614, 6,143,876, 6,132,992, 6,124,132, RE36,866, 6,114,143, 6,103,238, 6,060,254, 6,039,684, 6,030,772, 6,020,468, 6,013,484, 6,008,044, 5,998,132, 5,994,515, 5,993,812, 5,985,545, 5,981,278, 5,958,765, 5,939,277, 5,928,930, 5,922,325, 5,919,457, 5,916,806, 5,914,109, 5,911,989, 5,906,936, 5,889,158, 5,876,716, 5,874,226, 5,872,012, 5,871,732, 5,866,694, 5,854,400, 5,849,583, 5,849,288, 5,840,480, 5,840,305, 5,834,599, 5,831,034, 5,827,723, 5,821,047, 5,817,767, 5,817,458, 5,804,440, 5,795,572, 5,783,670, 5,776,703, 5,773,225, 5,766,944, 5,753,503, 5,750,373, 5,747,641, 5,736,341, 5,731,189, 5,707,814, 5,702,707, 5,698,178, 5,695,927, 5,665,536, 5,658,745, 5,652,138, 5,645,836, 5,635,345, 5,618,922, 5,610,035, 5,607,847, 5,604,092, 5,601,819, 5,597,896, 5,597,688, 5,591,829, 5,558,865, 5,514,541, 5,510,264, 5,478,753, 5,374,518, 5,374,516, 5,344,755, 5,332,567, 5,300,433, 5,296,347, 5,286,852, 5,264,221, 5,260,308, 5,256,561, 5,254,457, 5,230,998, 5,227,159, 5,223,408, 5,217,895, 5,180,660, 5,173,399, 5,169,752, 5,166,050, 5,156,951, 5,140,105, 5,135,864, 5,120,640, 5,108,904, 5,104,790, 5,049,389, 5,030,718, 5,030,555, 5,004,697, 4,983,529, 4,888,290, 4,886,742 and 4,853,326, are also useful for the present invention.
The vectors used in accordance with the present invention should typically be chosen such that they contain a suitable gene regulatory region, such as a promoter or enhancer, such that the proteins of the invention can be expressed.
For example, when the aim is to express the proteins of the invention in vitro, or in cultured cells, or in any prokaryotic or eukaryotic system for the purpose of producing the protein(s), then any suitable vector can be used depending on the application. For example, plasmids, viral vectors, bacterial vectors, protozoal vectors, insect vectors, baculovirus expression vectors, yeast vectors, mammalian cell vectors, and the like, can be used. Suitable vectors can be selected by the skilled artisan taking into consideration the characteristics of the vector and the requirements for expressing the proteins under the identified circumstances.
When the aim is to express the proteins of the invention in vivo in a subject, for example in order to generate an immune response against an antigen and/or protective immunity, expression vectors that are suitable for expression on that subject, and that are safe for use in vivo, should be chosen. In an advantageous embodiment, the antigen is an HIV-antigen. For example, in some embodiments it may be desired to express the proteins of the invention in a laboratory animal, such as for pre-clinical testing of the immunogenic compositions and vaccines of the invention. In other embodiments, it will be desirable to express the proteins of the invention in human subjects, such as in clinical trials and for actual clinical use of the immunogenic compositions and vaccine of the invention. Any vectors that are suitable for such uses can be employed, and it is well within the capabilities of the skilled artisan to select a suitable vector. In some embodiments it may be preferred that the vectors used for these in vivo applications are attenuated to vector from amplifying in the subject. For example, if plasmid vectors are used, preferably they will lack an origin of replication that functions in the subject so as to enhance safety for in vivo use in the subject. If viral vectors are used, preferably they are attenuated or replication-defective in the subject, again, so as to enhance safety for in vivo use in the subject.
In preferred embodiments of the present invention viral vectors are used. Viral expression vectors are well known to those skilled in the art and include, for example, viruses such as adenoviruses, adeno-associated viruses (AAV), alphaviruses, herpesviruses, retroviruses and poxviruses, including avipox viruses, attenuated poxviruses, vaccinia viruses, and particularly, the modified vaccinia Ankara virus (MVA; ATCC Accession No. VR-1566). Such viruses, when used as expression vectors are innately non-pathogenic in the selected subjects such as humans or have been modified to render them non-pathogenic in the selected subjects. For example, replication-defective adenoviruses and alphaviruses are well known and can be used as gene delivery vectors.
The present invention relates to recombinant vesicular stomatitis (VSV) vectors, however, other vectors may be contemplated in other embodiments of the invention such as, but not limited to, prime boost administration which may comprise administration of a recombinant VSV vector in combination with another recombinant vector expressing one or more HIV epitopes.
VSV is a very practical, safe, and immunogenic vector for conducting animal studies, and an attractive candidate for developing vaccines for use in humans. VSV is a member of the Rhabdoviridae family of enveloped viruses containing a nonsegmented, negative-sense RNA genome. The genome is composed of 5 genes arranged sequentially 3′-N-P-M-G-L-5′, each encoding a polypeptide found in mature virions. Notably, the surface glycoprotein G is a transmembrane polypeptide that is present in the viral envelope as a homotrimer, and like Env, it mediates cell attachment and infection.
General procedures for recovery of non-segmented negative-stranded RNA viruses according to the invention can be summarized as follows. A cloned DNA equivalent (which is positive-strand, message sense) of the desired viral genome is placed between a suitable DNA-dependent RNA polymerase promoter (e.g., a T7, T3 or SP6 RNA polymerase promoter) and a self-cleaving ribozyme sequence (e.g., the hepatitis delta ribozyme) which is inserted into a suitable transcription vector (e.g. a propagatable bacterial plasmid). This transcription vector provides the readily manipulable DNA template from which the RNA polymerase (e.g., T7 RNA polymerase) can faithfully transcribe a single-stranded RNA copy of the viral antigenome (or genome) with the precise, or nearly precise, 5′ and 3′ termini. The orientation of the viral DNA copy of the genome and the flanking promoter and ribozyme sequences determine whether antigenome or genome RNA equivalents are transcribed.
Also required for rescue of new virus progeny according to the invention are virus-specific trans-acting support proteins needed to encapsidate the naked, single-stranded viral antigenome or genome RNA transcripts into functional nucleocapsid templates. These generally include the viral nucleocapsid (N) protein, the polymerase-associated phosphoprotein (P) and the polymerase (L) protein.
Functional nucleocapsid serves as a template for genome replication, transcription of all viral mRNAs, and accumulation of viral proteins, triggering ensuing events in the viral replication cycle including virus assembly and budding. The mature virus particles contain the viral RNA polymerase necessary for further propagation in susceptible cells.
Certain attenuated viruses selected for rescue require the addition of support proteins, such as G and M for virus assembly and budding. For example, the attenuated VSV may be a propagation-defective VSV vector comprising a deletion of sequence encoding either all of the G protein (AG) or most of the G protein ectodomain (Gstem). Both AG and Gstem are unable to spread beyond primary infected cells in vivo. This results in a virus that can propagate only in the presence of transcomplementing G protein. Typically, although not necessarily exclusively, rescue of non-segmented negative-stranded RNA viruses also requires an RNA polymerase to be expressed in host cells carrying the viral cDNA, to drive transcription of the cDNA-containing transcription vector and of the vectors encoding the support proteins. Within the present invention, rescue of attenuated VSV typically involves transfecting host cells with: a viral cDNA expression vector containing a polynucleotide encoding a genome or antigenome of the attenuated VSV; one or more support plasmids encoding N, P, L and G proteins of VSV; and a plasmid encoding a DNA-dependent RNA polymerase, such as T7 RNA polymerase. The VSV G protein encoded by the support plasmid employed during viral rescue may be encoded by a native VSV G gene. However, the VSV G protein of a support plasmid used during viral rescue may be encoded by an optimized VSV G gene. In some embodiments, the cells are also transfected with a support plasmid encoding an M protein of VSV. The transfected cells are grown in culture, and attenuated VSV is rescued from the culture. The rescued material may then be co-cultured with plaque expansion cells for further viral expansion, as described in further detail below.
The host cells used for viral rescue are often impaired in their ability to support further viral expansion. Therefore, the method of producing attenuated VSV in a cell culture typically further includes infecting plaque expansion cells with the rescued, attenuated VSV. In some embodiments of the present invention, cells expressing VSV G protein encoded by an optimized VSV G gene are infected with the rescued attenuated VSV; the infected cells are grown; and the attenuated VSV is recovered from the culture of infected cells.
In some embodiments of viral rescue, the polynucleotide encoding the genome or antigenome of the attenuated VSV is introduced into the cell in the form of a viral cDNA expression vector that includes the polynucleotide operatively linked to an expression control sequence to direct synthesis of RNA transcripts from the cDNA expression vector. In some embodiments, the expression control sequence is a suitable DNA-dependent RNA polymerase promoter (e.g., a 17, T3 or SP6 RNA polymerase promoter). In some embodiments, the support plasmids, as well as the viral cDNA expression vector used during viral rescue are under the control of a promoter of the DNA-dependent RNA polymerase. For example, in embodiments where the RNA polymerase is T7 RNA polymerase, the support plasmids and the viral cDNA expression vector would preferably be under the control of a T7 promoter. In some other embodiments, the expression of the DNA-dependent RNA polymerase is under the control of a cytomegalovirus-derived RNA polymerase Il promoter. The immediate-early human cytomegalovirus [hCMV] promoter and enhancer is described, for e.g., in U.S. Pat. No. 5,168,062, incorporated herein by reference.
In some embodiments, the method for recovering attenuated VSV from cDNA involves introducing a viral cDNA expression vector encoding a genome or antigenome of the subject virus into a host cell, and coordinately introducing: a polymerase expression vector encoding and directing expression of an RNA polymerase. Useful RNA polymerases in this context include, but are not limited to, a T7, T3, or SP6 phage polymerase. The host cells also express, before, during, or after coordinate introduction of the viral cDNA expression vector, the polymerase expression vector and the N, P, L, M and G support proteins necessary for production of mature attenuated VSV particles in the host cell. Typically, the viral cDNA expression vector and polymerase expression vector will be coordinately transfected into the host cell with one or more additional expression vector(s) that encode(s) and direct(s) expression of the support proteins. The support proteins may be wild-type or mutant proteins of the virus being rescued, or may be selected from corresponding support protein(s) of a heterologous non-segmented negative-stranded RNA virus. In alternate embodiments, additional viral proteins may be co-expressed in the host cell, for example a polymerase elongation factor (such as M2-1 for RSV) or other viral proteins that may enable or enhance recovery or provide other desired results within the subject methods and compositions. In other embodiments, one or more of the support protein(s) may be expressed in the host cell by constitutively expressing the protein(s) in the host cell, or by co-infection of the host cell with a helper virus encoding the support protein(s).
The viral cDNA vector is introduced into a host cell transiently expressing an RNA polymerase and the following VSV support proteins: an N protein, a P protein, an L protein, an M protein and a G protein. Each of the RNA polymerase and the N, P, L, M and G proteins may be expressed from one or more transfected expression vector(s). Often, each of the RNA polymerase and the support proteins will be expressed from separate expression vectors, commonly from transient expression plasmids. Following a sufficient time and under suitable conditions, an assembled infectious, attenuated VSV is rescued from the host cells.
To produce infectious, attenuated VSV particles from a cDNA-expressed genome or antigenome, the genome or antigenome is coexpressed with those viral proteins necessary to produce a nucleocapsid capable of RNA replication, and render progeny nucleocapsids competent for both RNA replication and transcription. Such viral proteins include the N, P and L proteins. In the instant invention, attenuated VSV vectors with lost G function also require the addition of the G viral protein. Moreover, an M protein may also be added for a productive infection. The G and M viral proteins can be supplied by coexpression. In some embodiments, the VSV G support plasmid employed during viral rescue contains a non-optimized VSV G gene. However, in other embodiments, as described below, the VSV G support plasmid employed during viral rescue contains an optimized VSV G gene.
In certain embodiments of the invention, complementing sequences encoding proteins necessary to generate a transcribing, replicating viral nucleocapsid (i.e., L, P and N), as well as the M and G proteins are provided by expression plasmids. In other embodiments, such proteins are provided by one or more helper viruses. Such helper viruses can be wild type or mutant. In certain embodiments, the helper virus can be distinguished phenotypically from the virus encoded by the recombinant viral cDNA. For example, it may be desirable to provide monoclonal antibodies that react immunologically with the helper virus but not the virus encoded by the recombinant viral cDNA. Such antibodies can be neutralizing antibodies. In some embodiments, the antibodies can be used in affinity chromatography to separate the helper virus from the recombinant virus. To aid the procurement of such antibodies, mutations can be introduced into the viral cDNA to provide antigenic diversity from the helper virus, such as in a glycoprotein gene.
A recombinant viral genome or antigenome may be constructed for use in the present invention by, e.g., assembling cloned cDNA segments, representing in aggregate the complete genome or antigenome, by polymerase chain reaction or the like (PCR; described in, e.g., U.S. Pat. Nos. 4,683,195 and 4,683,202, and PCR Protocols: A Guide to Methods and Applications, Innis et al., eds., Academic Press, San Diego, 1990) of reverse-transcribed copies of viral mRNA or genome RNA. For example, a first construct may be generated which comprises cDNAs containing the left hand end of the antigenome, spanning from an appropriate promoter (e.g., T7, T3, or SP6 RNA polymerase promoter) and assembled in an appropriate expression vector (such as a plasmid, cosmid, phage, or DNA virus vector). The vector may be modified by mutagenesis and/or insertion of a synthetic polylinker containing unique restriction sites designed to facilitate assembly. The right hand end of the antigenome plasmid may contain additional sequences as desired, such as a flanking ribozyme and single or tandem T7 transcriptional terminators. The ribozyme can be hammerhead type, which would yield a 3′ end containing a single nonviral nucleotide, or can be any of the other suitable ribozymes such as that of hepatitis delta virus (Perrotta et al., Nature 350:434-436, 1991) that would yield a 31 end free of non-viral nucleotides.
Alternative means to construct cDNA encoding the viral genome or antigenome include reverse transcription-PCR using improved PCR conditions (e.g., as described in Cheng et al., Proc. Natl. Acad. Sci. USA 91/5695-5699, 1994, incorporated herein by reference) to reduce the number of subunit cDNA components to as few as one or two pieces. In other embodiments different promoters can be used (e.g., T3 or SPQ). Different DNA vectors (e.g., cosmids) can be used for propagation to better accommodate the larger size genome or antigenome.
As noted above, defined mutations can be introduced into an infectious viral clone by a variety of conventional techniques (e.g., site-directed mutagenesis) into a cDNA copy of the genome or antigenome. The use of genomic or antigenomic cDNA subfragments to assemble a complete genome or antigenome cDNA as described herein has the advantage that each region can be manipulated separately, where small cDNA constructs provide for better ease of manipulation than large cDNA constructs, and then readily assembled into a complete cDNA.
Certain of the attenuated viruses of the invention will be constructed or modified to limit the growth potential, replication competence, or infectivity of the recombinant virus. Such attenuated viruses and subviral particles are useful as vectors and immunogens, but do not pose certain risks that would otherwise attend administration of a fully infectious (i.e., having approximately a wild-type level of growth and/or replication competence) virus to a host. By attenuated, it is meant a virus or subviral particle that is limited in its ability to grow or replicate in a host cell or a mammalian subject, or is otherwise defective in its ability to infect and/or propagate in or between cells. By way of example, AG and G stem are attenuated viruses that are propagation-defective, but replication competent. Often, attenuated viruses and subviral particles will be employed as “vectors”, as described in detail herein below.
Thus, various methods and compositions are provided for producing attenuated VSV particles. In more detailed embodiments, the attenuated virus will exhibit growth, replication and/or infectivity characteristics that are substantially impaired in comparison to growth, replication and/or infectivity of a corresponding wild-type or parental virus. In this context, growth, replication, and/or infectivity may be impaired in vitro and/or in vivo by at least approximately 10-20%, 20-50%, 50-75% and up to 95% or greater compared to wild-type or parental growth, replication and/or infectivity levels. In some embodiments, viruses with varying degrees of growth or replication defects may be rescued using a combined heat shock/T7-plasmid rescue system described in detail below. Exemplary strains include highly attenuated strains of VSV that incorporate modifications as described below (e.g., a C-terminal G protein truncation, or translocated genes) (see, e.g., Johnson et al., J. Virol. 71:5060-5078, 1997, Schnell et al., Proc. Natl. Acad. Sci. USA 93:11359-11365, 1996; Schnell et al., Cell 90:849-857, 1997; Roberts et al., J. Virol. 72:4704-4711, 1998; and Rose et al., Cell 0.106:539-549, 2001, each incorporated herein by reference).
The VSVs of U.S. Pat. Nos. 7,468,274; 7,419,829; 7,419,674; 7,344,838; 7,332,316; 7,329,807; 7,323,337; 7,259,015; 7,244,818; 7,226,786; 7,211,247; 7,202,079; 7,198,793; 7,198,784; 7,153,510; 7,070,994; 6,969,598; 6,958,226; RE38,824; PP15,957; 6,890,735; 6,887,377; 6,867,326; 6,867,036; 6,858,205; 6,835,568; 6,830,892; 6,818,209; 6,790,641; 6,787,520; 6,743,620; 6,740,764; 6,740,635; 6,740,320; 6,682,907; 6,673,784; 6,673,572; 6,669,936; 6,653,103; 6,607,912; 6,558,923; 6,555,107; 6,533,855; 6,531,123; 6,506,604; 6,500,623; 6,497,873; 6,489,142; 6,410,316; 6,410,313; 6,365,713; 6,348,312; 6,326,487; 6,312,682; 6,303,331; 6,277,633; 6,207,455; 6,200,811; 6,190,650; 6,171,862; 6,143,290; 6,133,027; 6,121,434; 6,103,462; 6,069,134; 6,054,127; 6,034,073; 5,969,211; 5,935,822; 5,888,727; 5,883,081; 5,876,727; 5,858,740; 5,843,723; 5,834,256; 5,817,491; 5,792,604; 5,789,229; 5,773,003; 5,763,406; 5,760,184; 5,750,396; 5,739,018; 5,698,446; 5,686,279; 5,670,354; 5,540,923; 5,512,421; 5,090,194; 4,939,176; 4,738,846; 4,622,292; 4,556,556 and 4,396,628 may be contemplated by the present invention.
Canine distemper virus (CDV) is a member of the Morbillivirus genus, which also includes measles virus (MV), rinderpest virus (RPV), peste des petits ruminants virus and morbilliviruses that infect aquatic mammals. CDV infection has been observed in monkey colonies indicating that its host range can extend to, but so far, there is no conclusive evidence linking CDV to human disease in spite of its speculative association to illness of unknown etiology. Lab-adapted CDV has been injected into humans without causing symptoms of infection suggesting that humans are a non-permissive host for CDV, which is consistent with recent studies showing that mutations facilitating both entry and replication are needed for CDV to efficiently adapt to human cells.
CDV enters host cells through attachment of H to specific cell receptors and subsequent F-mediated fusion of viral envelope and cell membrane. Wild-type CDV isolates primarily target signaling lymphocyte activation molecule (SLAM) and nectin-4 positive cells while vaccine strains of CDV gain broader cell tropisms besides recognizing these two receptors (ref 1: The morbillivirus receptor SLAM (CD150). Tatsuo H, Yanagi Y. Microbiol Immunol. 2002; 46(3):135-42. Ref 2: Dog nectin-4 is an epithelial cell receptor for canine distemper virus that facilitates virus entry and syncytia formation. Noyce R S, Delpeut S, Richardson C D. Virology. 2013 Feb. 5; 436(1):210-20). Therefore, cell tropisms of CDV vectors differ depending on usage of wild-type or vaccine CDV H proteins. In addition, extra specificity determinants can be added to H protein ectodomain for specific cancer cell targeting and natural receptor interactions deactivated by H mutations, which has been developed in MV-based oncolytic vector research (ref: Paramyxovirus entry and targeted vectors for cancer therapy. Cattaneo R, PLoS Pathog. 2010 Jun. 24; 6(6)). Cell retargeting can also be achieved through F modifications. Because F function is activated after protease cleavage, paramyxovirus vectors including MV and Sendai virus can be modified to retarget cancer cells through cancer-specific cleavage of F (ref 1: Generation of a recombinant Sendai virus that is selectively activated and lyses human tumor cells expressing matrix metalloproteinases. Kinoh H, Inoue M, Washizawa K, Yamamoto T, Fujikawa S, et al. Gene Ther. 2004; 11:1137-1145. Ref 2: Oncolytic efficacy and enhanced safety of measles virus activated by tumor-secreted matrix metalloproteinases. Springfeld C, von Messling V, Frenzke M, Ungerechts G, Buchholz C J, Cattaneo R. Cancer Res. 2006; 66:7694-7700). CDV polymerase protein L has genome transcription and replication functions. Modifications in L of vaccine or oncolytic CDV vectors can change viral replication ability, which can serve as a tool to modulate level of CDV attenuation (ref: Development of a challenge-protective vaccine concept by modification of the viral RNA-dependent RNA polymerase of canine distemper virus. Silin D, Lyubomska O, Ludlow M, Duprex W P, Rima B K. J Virol. 2007 December; 81(24):13649-58).
Recombinant strains of CDV may be developed, for example, as described by, Miura R, Kooriyama T, Yoneda M, Takenaka A, Doki M, Goto Y, et al. (2015) Efficacy of Recombinant Canine Distemper Virus Expressing Leishmania Antigen against Leishmania Challenge in Dogs. PLoS Negl Trop Dis 9(7): e0003914. doi:10.1371/journal.pntd.0003914. Briefly, an antigen of interest may be introduced into a restriction site of a full-length cDNA of a CDV strain RNA genome. CDV rescue may be accomplished by transfecting HEK293 cells infected with MVA-TV with a full-genome plasmid, together with expression plasmids encoding viral nucleoprotein (N), phosphoprotein (P), and large protein (L) (pKS-N, pKS-P, and pGEM-L, respectively), using FuGENE6 Transfection Reagent (Invitrogen, Carlsbad, Calif., USA). Two days later, the transfected HEK293 cells were overlain with B95a cells. Syncytia formed by the rescued viruses were observed approximately 3 days later. The viruses were harvested, and their titers determined with the limiting dilution method and expressed as the 50% tissue culture infective dose (TCID 50 ).
The CDVs of U.S. Pat. Nos. 9,526,780; 9,505,812; 9,505,807; 9,327,137; 8,709,713; 8,309,531; 7,951,587; 6,664,066; 6,497,882; 6,368,603; 6,328,975; 6,309,647; 6,172,979; 5,843,456 and 5,756,102 may be contemplated by the present invention.
The nucleotide sequences and vectors of the invention can be delivered to cells, for example if aim is to express and the HIV-1 antigens in cells in order to produce and isolate the expressed proteins, such as from cells grown in culture. For expressing the proteins in cells any suitable transfection, transformation, or gene delivery methods can be used. Such methods are well known by those skilled in the art, and one of skill in the art would readily be able to select a suitable method depending on the nature of the nucleotide sequences, vectors, and cell types used. For example, transfection, transformation, microinjection, infection, electroporation, lipofection, or liposome-mediated delivery could be used. Expression of the proteins can be carried out in any suitable type of host cells, such as bacterial cells, yeast, insect cells, and mammalian cells. The proteins of the invention can also be expressed using including in vitro transcription/translation systems. All of such methods are well known by those skilled in the art, and one of skill in the art would readily be able to select a suitable method depending on the nature of the nucleotide sequences, vectors, and cell types used.
In preferred embodiments, the nucleotide sequences, proteins of the invention are administered in vivo, for example where the aim is to produce an immunogenic response in a subject. A “subject” in the context of the present invention may be any animal. For example, in some embodiments it may be desired to express the transgenes of the invention in a laboratory animal, such as for pre-clinical testing of the HIV-1 immunogenic compositions and vaccines of the invention. In other embodiments, it will be desirable to express the proteins of the invention in human subjects, such as in clinical trials and for actual clinical use of the immunogenic compositions and vaccine of the invention. In preferred embodiments the subject is a human, for example a human that is infected with, or is at risk of infection with, HIV-1.
For such in vivo applications the nucleotide sequences, proteins of the invention are preferably administered as a component of an immunogenic composition which may comprise the nucleotide sequences and/or antigens of the invention in admixture with a pharmaceutically acceptable carrier. The immunogenic compositions of the invention are useful to stimulate an immune response against HIV-1 and may be used as one or more components of a prophylactic or therapeutic vaccine against HIV-1 for the prevention, amelioration or treatment of AIDS. The nucleic acids and vectors of the invention are particularly useful for providing genetic vaccines, i.e. vaccines for delivering the nucleic acids encoding the proteins of the invention to a subject, such as a human, such that the proteins are then expressed in the subject to elicit an immune response.
The compositions of the invention may be injectable suspensions, solutions, sprays, lyophilized powders, syrups, elixirs and the like. Any suitable form of composition may be used. To prepare such a composition, a nucleic acid or vector of the invention, having the desired degree of purity, is mixed with one or more pharmaceutically acceptable carriers and/or excipients. The carriers and excipients must be “acceptable” in the sense of being compatible with the other ingredients of the composition. Acceptable carriers, excipients, or stabilizers are nontoxic to recipients at the dosages and concentrations employed, and include, but are not limited to, water, saline, phosphate buffered saline, dextrose, glycerol, ethanol, or combinations thereof, buffers such as phosphate, citrate, and other organic acids; antioxidants including ascorbic acid and methionine; preservatives (such as octadecyldimethylbenzyl ammonium chloride; hexamethonium chloride; benzalkonium chloride, benzethonium chloride; phenol, butyl or benzyl alcohol; alkyl parabens such as methyl or propyl paraben; catechol; resorcinol; cyclohexanol; 3-pentanol; and m-cresol); low molecular weight (less than about 10 residues) polypeptide; proteins, such as serum albumin, gelatin, or immunoglobulins; hydrophilic polymers such as polyvinylpyrrolidone; amino acids such as glycine, glutamine, asparagine, histidine, arginine, or lysine; monosaccharides, disaccharides, and other carbohydrates including glucose, mannose, or dextrins; chelating agents such as EDTA; sugars such as sucrose, mannitol, trehalose or sorbitol; salt-forming counter-ions such as sodium; metal complexes (e.g., Zn-protein complexes); and/or non-ionic surfactants such as TWEEN™, PLURONICS™ or polyethylene glycol (PEG).
An immunogenic or immunological composition can also be formulated in the form of an oil-in-water emulsion. The oil-in-water emulsion can be based, for example, on light liquid paraffin oil (European Pharmacopea type); isoprenoid oil such as squalane, squalene, EICOSANE™ or tetratetracontane; oil resulting from the oligomerization of alkene(s), e.g., isobutene or decene; esters of acids or of alcohols containing a linear alkyl group, such as plant oils, ethyl oleate, propylene glycol di(caprylate/caprate), glyceryl tri(caprylate/caprate) or propylene glycol dioleate; esters of branched fatty acids or alcohols, e.g., isostearic acid esters. The oil advantageously is used in combination with emulsifiers to form the emulsion. The emulsifiers can be nonionic surfactants, such as esters of sorbitan, mannide (e.g., anhydromannitol oleate), glycerol, polyglycerol, propylene glycol, and oleic, isostearic, ricinoleic, or hydroxystearic acid, which are optionally ethoxylated, and polyoxypropylene-polyoxyethylene copolymer blocks, such as the Pluronic® products, e.g., L121. The adjuvant can be a mixture of emulsifier(s), micelle-forming agent, and oil such as that which is commercially available under the name Provax® (IDEC Pharmaceuticals, San Diego, Calif.).
The immunogenic compositions of the invention can contain additional substances, such as wetting or emulsifying agents, buffering agents, or adjuvants to enhance the effectiveness of the vaccines (Remington's Pharmaceutical Sciences, 18th edition, Mack Publishing Company, (ed.) 1980).
Adjuvants may also be included. Adjuvants include, but are not limited to, mineral salts (e.g., AlK(SO 4 ) 2 , AlNa(SO 4 ) 2 , AlNH(SO 4 ) 2 , silica, alum, Al(OH) 3 , Ca 3 (PO 4 ) 2 , kaolin, or carbon), polynucleotides with or without immune stimulating complexes (ISCOMs) (e.g., CpG oligonucleotides, such as those described in Chuang, T. H. et al, (2002) J. Leuk. Biol. 71(3): 538-44; Ahmad-Nejad, P. et al (2002) Eur. J. Immunol. 32(7): 1958-68; poly IC or poly AU acids, polyarginine with or without CpG (also known in the art as IC31; see Schellack, C. et al (2003) Proceedings of the 34th Annual Meeting of the German Society of Immunology; Lingnau, K. et al (2002) Vaccine 20(29-30): 3498-508), JuvaVax™ (U.S. Pat. No. 6,693,086), certain natural substances (e.g., wax D from Mycobacterium tuberculosis , substances found in Cornyebacterium parvum, Bordetella pertussis , or members of the genus Brucella ), flagellin (Toll-like receptor 5 ligand; see McSorley, S. J. et al (2002) J. Immunol. 169(7): 3914-9), saponins such as QS21, QS17, and QS7 (U.S. Pat. Nos. 5,057,540; 5,650,398; 6,524,584; 6,645,495), monophosphoryl lipid A, in particular, 3-de-O-acylated monophosphoryl lipid A (3D-MPL), imiquimod (also known in the art as IQM and commercially available as Aldara®; U.S. Pat. Nos. 4,689,338; 5,238,944; Zuber, A. K. et al (2004) 22(13-14): 1791-8), and the CCR5 inhibitor CMPD167 (see Veazey, R. S. et al (2003) J. Exp. Med. 198: 1551-1562).
Aluminum hydroxide or phosphate (alum) are commonly used at 0.05 to 0.1% solution in phosphate buffered saline. Other adjuvants that can be used, especially with DNA vaccines, are cholera toxin, especially CTA1-DD/ISCOMs (see Mowat, A. M. et al (2001) J. Immunol. 167(6): 3398-405), polyphosphazenes (Allcock, H. R. (1998) App. Organometallic Chem. 12(10-11): 659-666; Payne, L. G. et al (1995) Pharm. Biotechnol. 6: 473-93), cytokines such as, but not limited to, IL-2, IL-4, GM-CSF, IL-12, IL-15 IGF-1, IFN-α, IFN-β, and IFN-γ (Boyer et al., (2002) J. Liposome Res. 121:137-142; WO01/095919), immunoregulatory proteins such as CD40L (ADX40; see, for example, WO03/063899), and the CD1a ligand of natural killer cells (also known as CRONY or α-galactosyl ceramide; see Green, T. D. et al, (2003) J. Virol. 77(3): 2046-2055), immunostimulatory fusion proteins such as IL-2 fused to the Fc fragment of immunoglobulins (Barouch et al., Science 290:486-492, 2000) and co-stimulatory molecules B7.1 and B7.2 (Boyer), all of which can be administered either as proteins or in the form of DNA, on the same expression vectors as those encoding the antigens of the invention or on separate expression vectors.
In an advantageous embodiment, the adjuvants may be lecithin is combined with an acrylic polymer (Adjuplex-LAP), lecithin coated oil droplets in an oil-in-water emulsion (Adjuplex-LE) or lecithin and acrylic polymer in an oil-in-water emulsion (Adjuplex-LAO) (Advanced BioAdjuvants (ABA)).
The immunogenic compositions can be designed to introduce the nucleic acids or expression vectors to a desired site of action and release it at an appropriate and controllable rate. Methods of preparing controlled-release formulations are known in the art. For example, controlled release preparations can be produced by the use of polymers to complex or absorb the immunogen and/or immunogenic composition. A controlled-release formulation can be prepared using appropriate macromolecules (for example, polyesters, polyamino acids, polyvinyl, pyrrolidone, ethylenevinylacetate, methylcellulose, carboxymethylcellulose, or protamine sulfate) known to provide the desired controlled release characteristics or release profile. Another possible method to control the duration of action by a controlled-release preparation is to incorporate the active ingredients into particles of a polymeric material such as, for example, polyesters, polyamino acids, hydrogels, polylactic acid, polyglycolic acid, copolymers of these acids, or ethylene vinylacetate copolymers. Alternatively, instead of incorporating these active ingredients into polymeric particles, it is possible to entrap these materials into microcapsules prepared, for example, by coacervation techniques or by interfacial polymerization, for example, hydroxymethylcellulose or gelatin-microcapsule and poly-(methylmethacrylate) microcapsule, respectively, in colloidal drug delivery systems (for example, liposomes, albumin microspheres, microemulsions, nano-particles and nanocapsules) or in macroemulsions. Such techniques are disclosed in New Trends and Developments in Vaccines, Voller et al. (eds.), University Park Press, Baltimore, Md., 1978 and Remington's Pharmaceutical Sciences, 16th edition.
Suitable dosages of the nucleic acids and expression vectors of the invention (collectively, the immunogens) in the immunogenic composition of the invention can be readily determined by those of skill in the art. For example, the dosage of the immunogens can vary depending on the route of administration and the size of the subject. Suitable doses can be determined by those of skill in the art, for example by measuring the immune response of a subject, such as a laboratry animal, using conventional immunological techniques, and adjusting the dosages as appropriate. Such techniques for measuring the immune response of the subject include but are not limited to, chromium release assays, tetramer binding assays, IFN-γ ELISPOT assays, IL-2 ELISPOT assays, intracellular cytokine assays, and other immunological detection assays, e.g., as detailed in the text “Antibodies: A Laboratory Manual” by Ed Harlow and David Lane.
When provided prophylactically, the immunogenic compositions of the invention are ideally administered to a subject in advance of HIV infection, or evidence of HIV infection, or in advance of any symptom due to AIDS, especially in high-risk subjects. The prophylactic administration of the immunogenic compositions can serve to provide protective immunity of a subject against HIV-1 infection or to prevent or attenuate the progression of AIDS in a subject already infected with HIV-1. When provided therapeutically, the immunogenic compositions can serve to ameliorate and treat AIDS symptoms and are advantageously used as soon after infection as possible, preferably before appearance of any symptoms of AIDS but may also be used at (or after) the onset of the disease symptoms.
The immunogenic compositions can be administered using any suitable delivery method including, but not limited to, intramuscular, intravenous, intradermal, mucosal, and topical delivery. Such techniques are well known to those of skill in the art. More specific examples of delivery methods are intramuscular injection, intradermal injection, and subcutaneous injection. However, delivery need not be limited to injection methods. Further, delivery of DNA to animal tissue has been achieved by cationic liposomes (Watanabe et al., (1994) Mol. Reprod. Dev. 38:268-274; and WO 96/20013), direct injection of naked DNA into animal muscle tissue (Robinson et al., (1993) Vaccine 11:957-960; Hoffman et al., (1994) Vaccine 12: 1529-1533; Xiang et al., (1994) Virology 199: 132-140; Webster et al., (1994) Vaccine 12: 1495-1498; Davis et al., (1994) Vaccine 12: 1503-1509; and Davis et al., (1993) Hum. Mol. Gen. 2: 1847-1851), or intradermal injection of DNA using “gene gun” technology (Johnston et al., (1994) Meth. Cell Biol. 43:353-365). Alternatively, delivery routes can be oral, intranasal or by any other suitable route. Delivery also be accomplished via a mucosal surface such as the anal, vaginal or oral mucosa.
Immunization schedules (or regimens) are well known for animals (including humans) and can be readily determined for the particular subject and immunogenic composition. Hence, the immunogens can be administered one or more times to the subject. Preferably, there is a set time interval between separate administrations of the immunogenic composition. While this interval varies for every subject, typically it ranges from 10 days to several weeks, and is often 2, 4, 6 or 8 weeks. For humans, the interval is typically from 2 to 6 weeks. The immunization regimes typically have from 1 to 6 administrations of the immunogenic composition, but may have as few as one or two or four. The methods of inducing an immune response can also include administration of an adjuvant with the immunogens. In some instances, annual, biannual or other long interval (5-10 years) booster immunization can supplement the initial immunization protocol.
The present methods also include a variety of prime-boost regimens, for example DNA prime-Adenovirus boost regimens. In these methods, one or more priming immunizations are followed by one or more boosting immunizations. The actual immunogenic composition can be the same or different for each immunization and the type of immunogenic composition (e.g., containing protein or expression vector), the route, and formulation of the immunogens can also be varied. For example, if an expression vector is used for the priming and boosting steps, it can either be of the same or different type (e.g., DNA or bacterial or viral expression vector). One useful prime-boost regimen provides for two priming immunizations, four weeks apart, followed by two boosting immunizations at 4 and 8 weeks after the last priming immunization. It should also be readily apparent to one of skill in the art that there are several permutations and combinations that are encompassed using the DNA, bacterial and viral expression vectors of the invention to provide priming and boosting regimens.
The prime-boost regimen can also include VSV vectors that derive their G protein protein from different serotype vesicular stomatitis viruses (Rose N F, Roberts A, Buonocore L, Rose J K. Glycoprotein exchange vectors based on vesicular stomatitis virus allow effective boosting and generation of neutralizing antibodies to a primary isolate of human immunodeficiency virus type 1. J Virol. 2000 December; 74(23):10903-10). The VSV vectors used in these examples contain a G protein derived from the Indiana serotype of VSV. Vectors can also be constructed to express epitopes in the context of G molecules derived from other VSV serotypes (i.e. vesicular stomatitis New Jersey virus or vesicular stomatitis Alagoas virus) or other vesiculoviruses (i.e. Chandipura virus, Cocal virus, Isfahan virus). Thus an epitope like the HIV MPER can be delivered in a prime in the context of a G molecule that is from the Indiana serotype and the immune system can be boosted with a vector that expresses epitopes in the context of second serotype like New Jersey. This circumvents anti-G immunity elicited by the prime, and helps focus the boost response agains the foreign epitope.
A specific embodiment of the invention provides methods of inducing an immune response against HIV in a subject by administering an immunogenic composition of the invention, preferably which may comprise an adenovirus vector containing DNA encoding one or more of the epitopes of the invention, one or more times to a subject wherein the epitopes are expressed at a level sufficient to induce a specific immune response in the subject. Such immunizations can be repeated multiple times at time intervals of at least 2, 4 or 6 weeks (or more) in accordance with a desired immunization regime.
The immunogenic compositions of the invention can be administered alone, or can be co-administered, or sequentially administered, with other HIV immunogens and/or HIV immunogenic compositions, e.g., with “other” immunological, antigenic or vaccine or therapeutic compositions thereby providing multivalent or “cocktail” or combination compositions of the invention and methods of employing them. Again, the ingredients and manner (sequential or co-administration) of administration, as well as dosages can be determined taking into consideration such factors as the age, sex, weight, species and condition of the particular subject, and the route of administration.
When used in combination, the other HIV immunogens can be administered at the same time or at different times as part of an overall immunization regime, e.g., as part of a prime-boost regimen or other immunization protocol. In an advantageous embodiment, the other HIV immunogen is env, preferably the HIV env trimer.
Many other HIV immunogens are known in the art, one such preferred immunogen is HIVA (described in WO 01/47955), which can be administered as a protein, on a plasmid (e.g., pTHr.HIVA) or in a viral vector (e.g., MVA.HIVA). Another such HIV immunogen is RENTA (described in PCT/US2004/037699), which can also be administered as a protein, on a plasmid (e.g., pTHr.RENTA) or in a viral vector (e.g., MVA.RENTA).
For example, one method of inducing an immune response against HIV in a human subject may comprise administering at least one priming dose of an HIV immunogen and at least one boosting dose of an HIV immunogen, wherein the immunogen in each dose can be the same or different, provided that at least one of the immunogens is an epitope of the present invention, a nucleic acid encoding an epitope of the invention or an expression vector, preferably a VSV vector, encoding an epitope of the invention, and wherein the immunogens are administered in an amount or expressed at a level sufficient to induce an HIV-specific immune response in the subject. The HIV-specific immune response can include an HIV-specific T-cell immune response or an HIV-specific B-cell immune response. Such immunizations can be done at intervals, preferably of at least 0-29 or more weeks.
Preclinical efficacy in the SHIV challenge model was observed following mucosal vaccination with a total dose of 2×10 8 pfu per ml. The vaccine dose may be split between two sites, such as mucosal surfaces in the nasal and oral cavities, where each received 1×10 8 pfu applied in a buffered solution. Dosages ranging from about 1×10 4 to 1×10 9 pfu per ml are also contemplated. Single doses are also contemplated. Alternatively, a avaccination schedule from about 0 to 40 weeks is contemplated. A vaccination schedule may be at 0, 4 and 29 weeks.
Preclinical efficacy in the SHIV challenge model was observed with a vaccination schedule of 0, 4, and 29 weeks. Other vaccination schedules are also contemplated.






SEQ ID NO: 1:






1
aaattaatac gactcactat agggagacca caacggtttc cctctagcgt tgtcttcgtc




61
tgatgagtcc gtgaggacga aactatagga aaggaattcc tatagtcACG AAGACAAACA



121
AACCATTATT ATCATTAAAA GGCTCAGGAG AAACTTTAAC AGTAATCAAA ATGTCTGTTA



181
CAGTCAAGAG AATCATTGAC AACACAGTCA TAGTTCCAAA ACTTCCTGCA AATGAGGATC



241
CAGTGGAATA CCCGGCAGAT TACTTCAGAA AATCAAAGGA GATTCCTCTT TACATCAATA



301
CTACAAAAAG TTTGTCAGAT CTAAGAGGAT ATGTCTACCA AGGCCTCAAA TCCGGAAATG



361
TATCAATCAT ACATGTCAAC AGCTACTTGT ATGGAGCATT GAAGGACATC CGGGGTAAGT



421
TGGATAAAGA TTGGTCAAGT TTCGGAATAA ACATCGGGAA GGCAGGGGAT ACAATCGGAA



481
TATTTGACCT TGTATCCTTG AAAGCCCTGG ACGGTGTACT TCCAGATGGA GTATCGGATG



541
CTTCCAGAAC CAGCGCAGAT GACAAATGGT TGCCTTTGTA TCTACTTGGC TTATACAGAG



601
TGGGCAGAAC ACAAATGCCT GAATACAGAA AAAGGCTCAT GGATGGGCTG ACAAATCAAT



661
GCAAAATGAT CAATGAACAG TTTGAACCTC TTGTGCCAGA AGGTCGTGAC ATTTTTGATG



721
TGTGGGGAAA TGACAGTAAT TACACAAAAA TTGTCGCTGC AGTGGACATG TTCTTCCACA



781
TGTTCAAAAA ACATGAATGT GCCTCGTTCA GATACGGAAC TATTGTTTCC AGATTCAAAG



841
ATTGTGCTGC ATTGGCAACA TTTGGACACC TCTGCAAAAT AACCGGAATG TCTACAGAAG



901
ATGTGACGAC CTGGATCTTG AACCGAGAAG TTGCAGATGA GATGGTCCAA ATGATGCTTC



961
CAGGCCAAGA AATTGACAAG GCTGATTCAT ACATGCCTTA TTTGATCGAC TTTGGATTGT



1021
CTTCTAAGTC TCCATATTCT TCCGTCAAAA ACCCTGCCTT CCACTTCTGG GGGCAATTGA



1081
CAGCTCTTCT GCTCAGATCC ACCAGAGCAA GGAATGCCCG ACAGCCTGAT GACATTGAGT



1141
ATACATCTCT TACTACAGCA GGTTTGTTGT ACGCTTATGC AGTAGGATCC TCTGCTGACT



1201
TGGCACAACA GTTTTGTGTT GGAGATAGCA AATACACTCC AGATGATAGT ACCGGAGGAT



1261
TGACGACTAA TGCACCGCCA CAAGGCAGAG ATGTGGTCGA ATGGCTCGGA TGGTTTGAAG



1321
ATCAAAACAG AAAACCGACT CCTGATATGA TGCAGTATGC GAAACGAGCA GTCATGTCAC



1381
TGCAAGGCCT AAGAGAGAAG ACAATTGGCA AGTATGCTAA GTCAGAGTTT GACAAATGAC



1441
CCTATAATTC TCAGATCACC TATTATATAT TATGCTAGCT ATGAAAAAAA CTAACAGATA



1501
TCATGGATAA TCTCACAAAA GTTCGTGAGT ATCTCAAGTC CTATTCTCGT CTAGATCAGG



1561
CGGTAGGAGA GATAGATGAG ATCGAAGCAC AACGAGCTGA AAAGTCCAAT TATGAGTTGT



1621
TCCAAGAGGA CGGAGTGGAA GAGCATACTA GGCCCTCTTA TTTTCAGGCA GCAGATGATT



1681
CTGACACAGA ATCTGAACCA GAAATTGAAG ACAATCAAGG CTTGTATGTA CCAGATCCGG



1741
AAGCTGAGCA AGTTGAAGGC TTTATACAGG GGCCTTTAGA TGACTATGCA GATGAGGACG



1801
TGGATGTTGT ATTCACTTCG GACTGGAAAC AGCCTGAGCT TGAATCCGAC GAGCATGGAA



1861
AGACCTTACG GTTGACATTG CCAGAGGGTT TAAGTGGAGA GCAGAAATCC CAGTGGCTTT



1921
TGACGATTAA AGCAGTCGTT CAAAGTGCCA AACACTGGAA TCTGGCAGAG TGCACATTTG



1981
AAGCATCGGG AGAAGGGGTC ATCATAAAAA AGCGCCAGAT AACTCCGGAT GTATATAAGG



2041
TCACTCCAGT GATGAACACA CATCCGTCCC AATCAGAAGC CGTATCAGAT GTTTGGTCTC



2101
TCTCAAAGAC ATCCATGACT TTCCAACCCA AGAAAGCAAG TCTTCAGCCT CTCACCATAT



2161
CCTTGGATGA ATTGTTCTCA TCTAGAGGAG AATTCATCTC TGTCGGAGGT AACGGACGAA



2221
TGTCTCATAA AGAGGCCATC CTGCTCGGTC TGAGGTACAA AAAGTTGTAC AATCAGGCGA



2281
GAGTCAAATA TTCTCTGTAG ACTAGTATGA AAAAAAGTAA CAGATATCAC AATCTAAGTG



2341
TTATCCCAAT CCATTCATCA TGAGTTCCTT AAAGAAGATT CTCGGTCTGA AGGGGAAAGG



2401
TAAGAAATCT AAGAAATTAG GGATCGCACC ACCCCCTTAT GAAGAGGACA CTAACATGGA



2461
GTATGCTCCG AGCGCTCCAA TTGACAAATC CTATTTTGGA GTTGACGAGA TGGACACTCA



2521
TGATCCGAAT CAATTAAGAT ATGAGAAATT CTTCTTTACA GTGAAAATGA CGGTTAGATC



2581
TAATCGTCCG TTCAGAACAT ACTCAGATGT GGCAGCCGCT GTATCCCATT GGGATCACAT



2641
GTACATCGGA ATGGCAGGGA AACGTCCCTT CTACAAGATC TTGGCTTTTT TGGGTTCTTC



2701
TAATCTAAAG GCCACTCCAG CGGTATTGGC AGATCAAGGT CAACCAGAGT ATCATGCTCA



2761
CTGTGAAGGC AGGGCTTATT TGCCACACAG AATGGGGAAG ACCCCTCCCA TGCTCAATGT



2821
ACCAGAGCAC TTCAGAAGAC CATTCAATAT AGGTCTTTAC AAGGGAACGA TTGAGCTCAC



2881
AATGACCATC TACGATGATG AGTCACTGGA AGCAGCTCCT ATGATCTGGG ATCATTTCAA



2941
TTCTTCCAAA TTTTCTGATT TCAGAGAGAA GGCCTTAATG TTTGGCCTGA TTGTCGAGAA



3001
AAAGGCATCT GGAGCTTGGG TCCTGGATTC TGTCAGCCAC TTCAAATGAG CTAGTCTAGC



3061
TTCCAGCTTC TGAACAATCC CCGGTTTACT CAGTCTCTCC TAATTCCAGC CTTTCGAACA



3121
ACTAATATCC TGTCTTCTCT ATCCCTATGA AAAAAACTAA CAGAGATCGA TCTGTTTCCT



3181
TGACACCAGG AGCCACCATG AAGTGCCTTT TGTACTTAGC TTTTTTATTC ATCGGGGTGA



3241
ATTGCAAGGC TAGCGCAGAG AATTTGTGGG TAACAGTCTA CTATGGAGTC CCTGTATGGA



3301
AGGATGCAGA GACAACATTG TTCTGTGCTA GTGACGCAAA GGCTTACGAG ACGGAGAAGC



3361
ACAATGTGTG GGCAACTCAC GCATGTGTCC CAACCGATCC AAATCCTCAA GAGATTCATC



3421
TAGAGAATGT GACTGAAGAA TTCAATATGT GGAAGAATAA TATGGTAGAG CAAATGCATA



3481
CAGATATCAT TAGTTTATGG GACCAGTCAC TTAAACCCTG CGTTAAATTG ACGCCTCTAT



3541
GTGTGACACT TCAATGTACT AATGTTACAA ACAACATAAC AGATGATATG AGAGGAGAAC



3601
TGAAGAACTG TAGTTTCAAC ATGACGACAG AGTTGCGTGA CAAGAAACAG AAAGTGTATT



3661
CACTATTCTA TCGGTTGGAT GTAGTACAGA TAAATGAGAA TCAAGGAAAC AGGTCCAACA



3721
ACTCTAACAA AGAGTACAGA CTTATTAATT GCAATACCAG TGCTATCACG CAAGCCTGCC



3781
CAAAGGTTTC ATTTGAACCA ATACCTATTC ATTATTGTGC ACCTGCTGGA TTCGCCATCC



3841
TCAAATGTAA AGACAAGAAG TTCAATGGAA CAGGACCCTG CCCATCAGTT TCAACCGTTC



3901
AGTGCACCCA CGGAATCAAG CCTGTAGTTA GTACTCAATT ATTGTTAAAT GGGAGCTTAG



3961
CTGAAGAAGA AGTTATGATT AGATCAGAGA ATATTACCAA TAATGCGAAG AACATCTTGG



4021
TTCAATTCAA TACTCCAGTC CAGATCAATT GCACAAGGCC TAATAATAAT ACCAGAAAGA



4081
GTATAAGAAT TGGGCCAGGA CAGGCATTCT ATGCAACAGG AGATATAATC GGAGACATTC



4141
GACAAGCGCA CTGCACTGTT TCTAAGGCCA CTTGGAATGA AACATTGGGT AAAGTTGTAA



4201
AGCAACTTCG GAAGCATTTC GGAAATAACA CAATTATTAG ATTTGCGAAC TCATCTGGAG



4261
GGGATCTGGA AGTGACAACA CACTCTTTCA ATTGCGGTGG CGAGTTCTTC TATTGTAATA



4321
CAAGTGGATT ATTTAACTCT ACTTGGATTT CAAATACCTC AGTCCAAGGA TCTAATTCAA



4381
CAGGGTCTAA CGATTCTATA ACATTACCTT GCCGTATAAA GCAAATTATT AATATGTGGC



4441
AAAGAATCGG GCAAGCGATG TATGCTCCAC CTATTCAAGG CGTGATTCGT TGCGTTTCAA



4501
ACATAACAGG GTTGATCCTG ACCAGGGATG GAGGCTCTAC CAATTCCACC ACCGAGACCT



4561
TCCGTCCCGG TGGCGGAGAT ATGCGGGATA ACTGGAGATC AGAGCTCTAT AAGTATAAGG



4621
TTGTGAAGAT TGAACCTCTT GGAGTTGCCC CTACAAGAGC AAAGAGAAGG GTGGTTGGCC



4681
GAGAGAAGAG AGCAGTTGGC ATCGGTGCTG TCTTTCTCGG ATTTCTTGGA GCAGCTGGAT



4741
CCACTATGGG AGCAGCATCA ATGACACTAA CAGTGCAGGC TAGAAATTTG CTTAGCGGAA



4801
TCGTTCAGCA GCAGAGCAAT TTACTAAGAG CAATTGAAGC ACAGCAACAT CTCTTAAAGT



4861
TGACGGTGTG GGGCATTAAA CAACTACAAG CGAGAGTGCT TGCCGTCGAA AGATATTTGC



4921
GAGACCAACA GCTATTGGGT ATTTGGGGTT GTTCTGGGAA ATTAATTTGC ACAACAAATG



4981
TTCCATGGAA CTCCTCCTGG AGTAATAGGA ATTTAAGTGA GATATGGGAC AACATGACAT



5041
GGTTGCAGTG GGACAAGGAA ATCTCAAATT ATACACAGAT AATCTATGGA TTATTAGAAG



5101
AGTCTCAGAA TCAGCAAGAG AAGAATGAAC AGGATTTGCT TGCATTGGAT AAGTGGGCTT



5161
CTCTATGGAA CTGGTTCGAT ATTAGTAATT GGCTCTGGTA TATTAAGAGC TCTATTGCCT



5221
CTTTTTTCTT TATCATAGGG TTAATCATTG GACTATTCTT GGTTCTCCGA GTTGGTATTT



5281
ATCTTTGCAT TAAATTAAAG CACACCAAGA AAAGACAGAT TTATACAGAC ATAGAGATGA



5341
ACCGACTTGG AAAGTAAAGC TCAAATCCTG CACAACAGAT TCTTCATGTT TGAACCAAAT



5401
CAACTTGTGA TATCATGCTC AAAGAGGCCT TAATTAAATT TTAATTTTTA ATTTTTATGA



5461
AAAAAACTAA CAGCAATCAT GGAAGTCCAC GATTTTGAGA CCGACGAGTT CAATGATTTC



5521
AATGAAGATG ACTATGCCAC AAGAGAATTC CTGAATCCCG ATGAGCGCAT GACGTACTTG



5581
AATCATGCTG ATTACAATTT GAATTCTCCT CTAATTAGTG ATGATATTGA CAATTTGATC



5641
AGGAAATTCA ATTCTCTTCC GATTCCCTCG ATGTGGGATA GTAAGAACTG GGATGGAGTT



5701
CTTGAGATGT TAACATCATG TCAAGCCAAT CCCATCTCAA CATCTCAGAT GCATAAATGG



5761
ATGGGAAGTT GGTTAATGTC TGATAATCAT GATGCCAGTC AAGGGTATAG TTTTTTACAT



5821
GAAGTGGACA AAGAGGCAGA AATAACATTT GACGTGGTGG AGACCTTCAT CCGCGGCTGG



5881
GGCAACAAAC CAATTGAATA CATCAAAAAG GAAAGATGGA CTGACTCATT CAAAATTCTC



5941
GCTTATTTGT GTCAAAAGTT TTTGGACTTA CACAAGTTGA CATTAATCTT AAATGCTGTC



6001
TCTGAGGTGG AATTGCTCAA CTTGGCGAGG ACTTTCAAAG GCAAAGTCAG AAGAAGTTCT



6061
CATGGAACGA ACATATGCAG GCTTAGGGTT CCCAGCTTGG GTCCTACTTT TATTTCAGAA



6121
GGATGGGCTT ACTTCAAGAA ACTTGATATT CTAATGGACC GAAACTTTCT GTTAATGGTC



6181
AAAGATGTGA TTATAGGGAG GATGCAAACG GTGCTATCCA TGGTATGTAG AATAGACAAC



6241
CTGTTCTCAG AGCAAGACAT CTTCTCCCTT CTAAATATCT ACAGAATTGG AGATAAAATT



6301
GTGGAGAGGC AGGGAAATTT TTCTTATGAC TTGATTAAAA TGGTGGAACC GATATGCAAC



6361
TTGAAGCTGA TGAAATTAGC AAGAGAATCA AGGCCTTTAG TCCCACAATT CCCTCATTTT



6421
GAAAATCATA TCAAGACTTC TGTTGATGAA GGGGCAAAAA TTGACCGAGG TATAAGATTC



6481
CTCCATGATC AGATAATGAG TGTGAAAACA GTGGATCTCA CACTGGTGAT TTATGGATCG



6541
TTCAGACATT GGGGTCATCC TTTTATAGAT TATTACGCTG GACTAGAAAA ATTACATTCC



6601
CAAGTAACCA TGAAGAAAGA TATTGATGTG TCATATGCAA AAGCACTTGC AAGTGATTTA



6661
GCTCGGATTG TTCTATTTCA ACAGTTCAAT GATCATAAAA AGTGGTTCGT GAATGGAGAC



6721
TTGCTCCCTC ATGATCATCC CTTTAAAAGT CATGTTAAAG AAAATACATG GCCTACAGCT



6781
GCTCAAGTTC AAGATTTTGG AGATAAATGG CATGAACTTC CGCTGATTAA ATGTTTTGAA



6841
ATACCCGACT TACTAGACCC ATCGATAATA TACTCTGACA AAAGTCATTC AATGAATAGG



6901
TCAGAGGTGT TGAAACATGT CCGAATGAAT CCGAACACTC CTATCCCTAG TAAAAAGGTG



6961
TTGCAGACTA TGTTGGACAC AAAGGCTACC AATTGGAAAG AATTTCTTAA AGAGATTGAT



7021
GAGAAGGGCT TAGATGATGA TGATCTAATT ATTGGTCTTA AAGGAAAGGA GAGGGAACTG



7081
AAGTTGGCAG GTAGATTTTT CTCCCTAATG TCTTGGAAAT TGCGAGAATA CTTTGTAATT



7141
ACCGAATATT TGATAAAGAC TCATTTCGTC CCTATGTTTA AAGGCCTGAC AATGGCGGAC



7201
GATCTAACTG CAGTCATTAA AAAGATGTTA GATTCCTCAT CCGGCCAAGG ATTGAAGTCA



7261
TATGAGGCAA TTTGCATAGC CAATCACATT GATTACGAAA AATGGAATAA CCACCAAAGG



7321
AAGTTATCAA ACGGCCCAGT GTTCCGAGTT ATGGGCCAGT TCTTAGGTTA TCCATCCTTA



7381
ATCGAGAGAA CTCATGAATT TTTTGAGAAA AGTCTTATAT ACTACAATGG AAGACCAGAC



7441
TTGATGCGTG TTCACAACAA CACACTGATC AATTCAACCT CCCAACGAGT TTGTTGGCAA



7501
GGACAAGAGG GTGGACTGGA AGGTCTACGG CAAAAAGGAT GGAGTATCCT CAATCTACTG



7561
GTTATTCAAA GAGAGGCTAA AATCAGAAAC ACTGCTGTCA AAGTCTTGGC ACAAGGTGAT



7621
AATCAAGTTA TTTGCACACA GTATAAAACG AAGAAATCGA GAAACGTTGT AGAATTACAG



7681
GGTGCTCTCA ATCAAATGGT TTCTAATAAT GAGAAAATTA TGACTGCAAT CAAAATAGGG



7741
ACAGGGAAGT TAGGACTTTT GATAAATGAC GATGAGACTA TGCAATCTGC AGATTACTTG



7801
AATTATGGAA AAATACCGAT TTTCCGTGGA GTGATTAGAG GGTTAGAGAC CAAGAGATGG



7861
TCACGAGTGA CTTGTGTCAC CAATGACCAA ATACCCACTT GTGCTAATAT AATGAGCTCA



7921
GTTTCCACAA ATGCTCTCAC CGTAGCTCAT TTTGCTGAGA ACCCAATCAA TGCCATGATA



7981
CAGTACAATT ATTTTGGGAC ATTTGCTAGA CTCTTGTTGA TGATGCATGA TCCTGCTCTT



8041
CGTCAATCAT TGTATGAAGT TCAAGATAAG ATACCGGGCT TGCACAGTTC TACTTTCAAA



8101
TACGCCATGT TGTATTTGGA CCCTTCCATT GGAGGAGTGT CGGGCATGTC TTTGTCCAGG



8161
TTTTTGATTA GAGCCTTCCC AGATCCCGTA ACAGAAAGTC TCTCATTCTG GAGATTCATC



8221
CATGTACATG CTCGAAGTGA GCATCTGAAG GAGATGAGTG CAGTATTTGG AAACCCCGAG



8281
ATAGCCAAGT TCCGAATAAC TCACATAGAC AAGCTAGTAG AAGATCCAAC CTCTCTGAAC



8341
ATCGCTATGG GAATGAGTCC AGCGAACTTG TTAAAGACTG AGGTTAAAAA ATGCTTAATC



8401
GAATCAAGAC AAACCATCAG GAACCAGGTG ATTAAGGATG CAACCATATA TTTGTATCAT



8461
GAAGAGGATC GGCTCAGAAG TTTCTTATGG TCAATAAATC CTCTGTTCCC TAGATTTTTA



8521
AGTGAATTCA AATCAGGCAC TTTTTTGGGA GTCGCAGACG GGCTCATCAG TCTATTTCAA



8581
AATTCTCGTA CTATTCGGAA CTCCTTTAAG AAAAAGTATC ATAGGGAATT GGATGATTTG



8641
ATTGTGAGGA GTGAGGTATC CTCTTTGACA CATTTAGGGA AACTTCATTT GAGAAGGGGA



8701
TCATGTAAAA TGTGGACATG TTCAGCTACT CATGCTGACA CATTAAGATA CAAATCCTGG



8761
GGCCGTACAG TTATTGGGAC AACTGTACCC CATCCATTAG AAATGTTGGG TCCACAACAT



8821
CGAAAAGAGA CTCCTTGTGC ACCATGTAAC ACATCAGGGT TCAATTATGT TTCTGTGCAT



8881
TGTCCAGACG GGATCCATGA CGTCTTTAGT TCACGGGGAC CATTGCCTGC TTATCTAGGG



8941
TCTAAAACAT CTGAATCTAC ATCTATTTTG CAGCCTTGGG AAAGGGAAAG CAAAGTCCCA



9001
CTGATTAAAA GAGCTACACG TCTTAGAGAT GCTATCTCTT GGTTTGTTGA ACCCGACTCT



9061
AAACTAGCAA TGACTATACT TTCTAACATC CACTCTTTAA CAGGCGAAGA ATGGACCAAA



9121
AGGCAGCATG GGTTCAAAAG AACAGGGTCT GCCCTTCATA GGTTTTCGAC ATCTCGGATG



9181
AGCCATGGTG GGTTCGCATC TCAGAGCACT GCAGCATTGA CCAGGTTGAT GGCAACTACA



9241
GACACCATGA GGGATCTGGG AGATCAGAAT TTCGACTTTT TATTCCAAGC AACGTTGCTC



9301
TATGCTCAAA TTACCACCAC TGTTGCAAGA GACGGATGGA TCACCAGTTG TACAGATCAT



9361
TATCATATTG CCTGTAAGTC CTGTTTGAGA CCCATAGAAG AGATCACCCT GGACTCAAGT



9421
ATGGACTACA CGCCCCCAGA TGTATCCCAT GTGCTGAAGA CATGGAGGAA TGGGGAAGGT



9481
TCGTGGGGAC AAGAGATAAA ACAGATCTAT CCTTTAGAAG GGAATTGGAA GAATTTAGCA



9541
CCTGCTGAGC AATCCTATCA AGTCGGCAGA TGTATAGGTT TTCTATATGG AGACTTGGCG



9601
TATAGAAAAT CTACTCATGC CGAGGACAGT TCTCTATTTC CTCTATCTAT ACAAGGTCGT



9661
ATTAGAGGTC GAGGTTTCTT AAAAGGGTTG CTAGACGGAT TAATGAGAGC AAGTTGCTGC



9721
CAAGTAATAC ACCGGAGAAG TCTGGCTCAT TTGAAGAGGC CGGCCAACGC AGTGTACGGA



9781
GGTTTGATTT ACTTGATTGA TAAATTGAGT GTATCACCTC CATTCCTTTC TCTTACTAGA



9841
TCAGGACCTA TTAGAGACGA ATTAGAAACG ATTCCCCACA AGATCCCAAC CTCCTATCCG



9901
ACAAGCAACC GTGATATGGG GGTGATTGTC AGAAATTACT TCAAATACCA ATGCCGTCTA



9961
ATTGAAAAGG GAAAATACAG ATCACATTAT TCACAATTAT GGTTATTCTC AGATGTCTTA



10021
TCCATAGACT TCATTGGACC ATTCTCTATT TCCACCACCC TCTTGCAAAT CCTATACAAG



10081
CCATTTTTAT CTGGGAAAGA TAAGAATGAG TTGAGAGAGC TGGCAAATCT TTCTTCATTG



10141
CTAAGATCAG GAGAGGGGTG GGAAGACATA CATGTGAAAT TCTTCACCAA GGACATATTA



10201
TTGTGTCCAG AGGAAATCAG ACATGCTTGC AAGTTCGGGA TTGCTAAGGA TAATAATAAA



10261
GACATGAGCT ATCCCCCTTG GGGAAGGGAA TCCAGAGGGA CAATTACAAC AATCCCTGTT



10321
TATTATACGA CCACCCCTTA CCCAAAGATG CTAGAGATGC CTCCAAGAAT CCAAAATCCC



10381
CTGCTGTCCG GAATCAGGTT GGGCCAATTA CCAACTGGCG CTCATTATAA AATTCGGAGT



10441
ATATTACATG GAATGGGAAT CCATTACAGG GACTTCTTGA GTTGTGGAGA CGGCTCCGGA



10501
GGGATGACTG CTGCATTACT ACGAGAAAAT GTGCATAGCA GAGGAATATT CAATAGTCTG



10561
TTAGAATTAT CAGGGTCAGT CATGCGAGGC GCCTCTCCTG AGCCCCCCAG TGCCCTAGAA



10621
ACTTTAGGAG GAGATAAATC GAGATGTGTA AATGGTGAAA CATGTTGGGA ATATCCATCT



10681
GACTTATGTG ACCCAAGGAC TTGGGACTAT TTCCTCCGAC TCAAAGCAGG CTTGGGGCTT



10741
CAAATTGATT TAATTGTAAT GGATATGGAA GTTCGGGATT CTTCTACTAG CCTGAAAATT



10801
GAGACGAATG TTAGAAATTA TGTGCACCGG ATTTTGGATG AGCAAGGAGT TTTAATCTAC



10861
AAGACTTATG GAACATATAT TTGTGAGAGC GAAAAGAATG CAGTAACAAT CCTTGGTCCC



10921
ATGTTCAAGA CGGTCGACTT AGTTCAAACA GAATTTAGTA GTTCTCAAAC GTCTGAAGTA



10981
TATATGGTAT GTAAAGGTTT GAAGAAATTA ATCGATGAAC CCAATCCCGA TTGGTCTTCC



11041
ATCAATGAAT CCTGGAAAAA CCTGTACGCA TTCCAGTCAT CAGAACAGGA ATTTGCCAGA



11101
GCAAAGAAGG TTAGTACATA CTTTACCTTG ACAGGTATTC CCTCCCAATT CATTCCTGAT



11161
CCTTTTGTAA ACATTGAGAC TATGCTACAA ATATTCGGAG TACCCACGGG TGTGTCTCAT



11221
GCGGCTGCCT TAAAATCATC TGATAGACCT GCAGATTTAT TGACCATTAG CCTTTTTTAT



11281
ATGGCGATTA TATCGTATTA TAACATCAAT CATATCAGAG TAGGACCGAT ACCTCCGAAC



11341
CCCCCATCAG ATGGAATTGC ACAAAATGTG GGGATCGCTA TAACTGGTAT AAGCTTTTGG



11401
CTGAGTTTGA TGGAGAAAGA CATTCCACTA TATCAACAGT GTTTAGCAGT TATCCAGCAA



11461
TCATTCCCGA TTAGGTGGGA GGCTGTTTCA GTAAAAGGAG GATACAAGCA GAAGTGGAGT



11521
ACTAGAGGTG ATGGGCTCCC AAAAGATACC CGAATTTCAG ACTCCTTGGC CCCAATCGGG



11581
AACTGGATCA GATCTCTGGA ATTGGTCCGA AACCAAGTTC GTCTAAATCC ATTCAATGAG



11641
ATCTTGTTCA ATCAGCTATG TCGTACAGTG GATAATCATT TGAAATGGTC AAATTTGCGA



11701
AAAAACACAG GAATGATTGA ATGGATCAAT AGACGAATTT CAAAAGAAGA CCGGTCTATA



11761
CTGATGTTGA AGAGTGACCT ACACGAGGAA AACTCTTGGA GAGATTAAAA AATCATGAGG



11821
AGACTCCAAA CTTTAAGTAT GAAAAAAACT TTGATCCTTA AGACCCTCTT GTGGTTTTTA



11881
TTTTTTATCT GGTTTTGTGG TCTTCGTggc cggcatggtc ccagcctcct cgctggcgcc



11941
ggctgggcaa cattccgagg ggaccgtccc ctcggtaatg gcgaatggga cctgctaaca



12001
aagcccgaaa ggaagctgag ttggctgctg ccaccgctga gcaataacta gcataacccc



12061
ttggggcctc taaacgggtc ttgaggggtt ttttgctgaa aggaggaact atatccggat



12121
gcggccgatc cggctgctaa caaagcccga aaggaagctg agttggctgc tgccaccgct



12181
gagcaataac tagcataacc ccttggggcc tctaaacggg tcttgagggg ttttttgctg



12241
aaaggaggaa ctatatccgg gttaacctgc attaatgaat cggccaacgc gcggggagag



12301
gcggtttgcg tattgggcgc tcttccgctt cctcgctcac tgactcgctg cgctcggtcg



12361
ttcggctgcg gcgagcggta tcagctcact caaaggcggt aatacggtta tccacagaat



12421
caggggataa cgcaggaaag aacatgtgag caaaaggcca gcaaaaggcc aggaaccgta



12481
aaaaggccgc gttgctggcg tttttccata ggctccgccc ccctgacgag catcacaaaa



12541
atcgacgctc aagtcagagg tggcgaaacc cgacaggact ataaagatac caggcgtttc



12601
cccctggaag ctccctcgtg cgctctcctg ttccgaccct gccgcttacc ggatacctgt



12661
ccgcctttct cccttcggga agcgtggcgc tttctcaatg ctcacgctgt aggtatctca



12721
gttcggtgta ggtcgttcgc tccaagctgg gctgtgtgca cgaacccccc gttcagcccg



12781
accgctgcgc cttatccggt aactatcgtc ttgagtccaa cccggtaaga cacgacttat



12841
cgccactggc agcagccact ggtaacagga ttagcagagc gaggtatgta ggcggtgcta



12901
cagagttctt gaagtggtgg cctaactacg gctacactag aaggacagta tttggtatct



12961
gcgctctgct gaagccagtt accttcggaa aaagagttgg tagctcttga tccggcaaac



13021
aaaccaccgc tggtagcggt ggtttttttg tttgcaagca gcagattacg cgcagaaaaa



13081
aaggatctca agaagatcct ttgatctttt ctacggggtc tgacgctcag tggaacgaaa



13141
actcacgtta agggattttg gtcatgagat tatcaaaaag gatcttcacc tagatccttt



13201
taaattaaaa atgaagtttt aaatcaatct aaagtatata tgagtaaact tggtctgaca



13261
gttaccaatg cttaatcagt gaggcaccta tctcagcgat ctgtctattt cgttcatcca



13321
tagttgcctg actccccgtc gtgtagataa ctacgatacg ggagggctta ccatctggcc



13381
ccagtgctgc aatgataccg cgagacccac gctcaccggc tccagattta tcagcaataa



13441
accagccagc cggaagggcc gagcgcagaa gtggtcctgc aactttatcc gcctccatcc



13501
agtctattaa ttgttgccgg gaagctagag taagtagttc gccagttaat agtttgcgca



13561
acgttgttgc cattgctaca ggcatcgtgg tgtcacgctc gtcgtttggt atggcttcat



13621
tcagctccgg ttcccaacga tcaaggcgag ttacatgatc ccccatgttg tgcaaaaaag



13681
cggttagctc cttcggtcct ccgatcgttg tcagaagtaa gttggccgca gtgttatcac



13741
tcatggttat ggcagcactg cataattctc ttactgtcat gccatccgta agatgctttt



13801
ctgtgactgg tgagtactca accaagtcat tctgagaata gtgtatgcgg cgaccgagtt



13861
gctcttgccc ggcgtcaata cgggataata ccgcgccaca tagcagaact ttaaaagtgc



13921
tcatcattgg aaaacgttct tcggggcgaa aactctcaag gatcttaccg ctgttgagat



13981
ccagttcgat gtaacccact cgtgcaccca actgatcttc agcatctttt actttcacca



14041
gcgtttctgg gtgagcaaaa acaggaaggc aaaatgccgc aaaaaaggga ataagggcga



14101
cacggaaatg ttgaatactc atactcttcc tttttcaata ttattgaagc atttatcagg



14161
gttattgtct catgagcgga tacatatttg aatgtattta gaaaaataaa caaatagggg



14221
ttccgcgcac atttccccga aaagtgccac ctgacgtc






































































































































































































































































































































































































































































































An annotated sequence of SEQ ID NO 1 is provided below. The coded protein is disclosed as SEQ ID NO: 2.






>T7-g10 Promoter


|





aa att act acg act cac tat agg gag acc aca acg gtt tcc ctc tag cgt tgt ctt cgt c
< 60


10 20 30 40 50




>Hammerhead Ribozyme


|


tg atg agt ccg tga gga cga aac tat agg aaa gga att cct ata gtc ACG AAG ACA AAC A
< 120

70 80 90 100 110




>VSV Leader


|


AA CCA TTA TTA TCA TTA AAA TGC TCA GGA GAA ACT TTA ACA GTA ATC AAA ATG TCT GTT A
< 180

130 140 150 160 170




CA GTC AAG AGA ATC ATT GAC AAC ACA GTC ATA GTT CCA AAA CTT CCT GCA AAT GAG GAT C
< 240

190 200 210 220 230




CA CTC GAA TAC CCG GCA GAT TAC TTC AGA AAA TCA AAG GAG ATT CCT CTT TAC ATC AAT A
< 300

250 260 270 280 290




CT ACA AAA AGT TTG TCA GAT CTA AGA GGA TAT GTC TAC CAA GGC CTC AAA TCC GGA AAT G
< 360

310 320 330 340 350




TA TCA ATC ATA CAT GTC AAC AGC TAC TTG TAT GGA GCA TTG AAG GAC ATC CGG GGT AAG T
< 420

370 380 390 400 410




TG GAT AAA GAT TGG TCA AGT TTC GGA ATA AAC ATC GGG AAG GCA GGG GAT ACA ATC GGA A
< 480

430 440 450 460 470




TA TTT GAC CTT GTA TCC TTG AAA GCC CTG GAC GGT GTA CTT CCA GAT GGA GTA TCG GAT G
< 540

490 500 510 520 530




CT TCC AGA ACC AGC GCA GAT GAC AAA TGG TTG CCT TTG TAT CTA CTT GGC TTA TAC AGA G
< 600

550 560 570 580 590




TG GGC AGA ACA CAA ATG CCT GAA TAC AGA AAA AGG CTC ATG GAT GGG CTG ACA AAT CAA T
< 660

610 620 630 640 650




GC AAA ATG ATC AAT GAA CAG TTT GAA CCT CTT GTG CCA GAA GGT CGT GAC ATT TTT GAT G
< 720

670 680 690 700 710




TG TGG GGA AAT GAC AGT AAT TAC ACA AAA ATT GTC GCT GCA GTG GAC ATG TTC TTC CAC A
< 780

730 740 750 760 770




>N


|


TG TTC AAA AAA CAT GAA TGT GCC TCG TTC AGA TAC GGA ACT ATT GTT TCC AGA TTC AAA G
< 840

790 800 810 820 830




AT TGT GCT GCA TTG GCA ACA TTT GGA CAC CTC TGC AAA ATA ACC GGA ATG TCT ACA GAA G
< 900

850 860 870 880 890




AT GTG ACG ACC TGG ATC TTG AAC CGA GAA GTT GCA GAT GAG ATG GTC CAA ATG ATG CTT C
< 960

910 920 930 940 950




CA GGC CAA GAA ATT GAC AAG GCT GAT TCA TAC ATG CCT TAT TTG ATC GAC TTT GGA TTG T
< 1020

970 980 990 1000 1010




CT TCT AAG TCT CCA TAT TCT TCC GTC AAA AAC CCT GCC TTC CAC TTC TGG GGG CAA TTG A
< 1080

1030 1040 1050 1060 1070




CA GCT CTT CTG CTC AGA TCC ACC AGA GCA AGG AAT GCC CGA CAG CCT GAT GAC ATT GAG T
< 1140

1090 1100 1110 1120 1130




AT ACA TCT CTT ACT ACA GCA GGT TTG TTG TAC GCT TAT GCA GTA GGA TCC TCT GCT GAC T
< 1200

1150 1160 1170 1180 1190




TG GCA CAA CAG TTT TGT GTT GGA GAT AGC AAA TAC ACT CCA GAT GAT AGT ACC GGA GGA T
< 1260

1210 1220 1230 1240 1250




TG ACG ACT AAT GCA CCG CCA CAA GGC AGA GAT GTG GTC GAA TGG CTC GGA TGG TTT GAA G
< 1320

1270 1280 1290 1300 1310




AT CAA AAC AGA AAA CCG ACT CCT GAT ATG ATG CAG TAT GCG AAA CGA GCA GTC ATG TCA C
< 1380

1330 1340 1350 1360 1370




TG CAA GGC CTA AGA GAG AAG ACA ATT GGC AAG TAT GCT AAG TCA GAG TTT GAC AAA TGA C
< 1440

1390 1400 1410 1420 1430




CC TAT AAT TCT CAG ATC ACC TAT TAT ATA TTA TGC TAG CTA TGA AAA AAA CTA ACA GAT A
< 1500

1450 1460 1470 1480 1490




TC ATG GAT AAT CTC ACA AAA GTT CGT GAG TAT CTC AAG TCC TAT TCT CGT CTA GAT CAG G
< 1560

1510 1520 1530 1540 1550




CG GTA GGA GAG ATA GAT GAG ATC GAA GCA CAA CGA GCT GAA AAG TCC AAT TAT GAG TTG T
< 1620

1570 1580 1590 1600 1610




TC CAA GAG GAC GGA GTG GAA GAG CAT ACT AGG CCC TCT TAT TTT CAG GCA GCA GAT GAT T
< 1680

1630 1640 1650 1660 1670




CT GAC ACA GAA TCT GAA CCA GAA ATT GAA GAC AAT CAA GGC TTG TAT GTA CCA GAT CCG G
< 1740

1690 1700 1710 1720 1730




AA GCT GAG CAA GTT GAA GGC TTT ATA CAG GGG CCT TTA GAT GAC TAT GCA GAT GAG GAC G
< 1800

1750 1760 1770 1780 1790




TG GAT GTT GTA TTC ACT TCG GAC TGG AAA CAG CCT GAG CTT GAA TCC GAC GAG CAT GGA A
< 1860

1810 1820 1830 1840 1850




>P


|


AG ACC TTA CGG TTG ACA TTG CCA GAG GGT TTA AGT GGA GAG CAG AAA TCC CAG TGG CTT T
< 1920

1870 1880 1890 1900 1910




TG ACG ATT AAA GCA GTC GTT CAA AGT GCC AAA CAC TGG AAT CTG GCA GAG TGC ACA TTT G
< 1980

1930 1940 1950 1960 1970




AA GCA TCG GGA GAA GGG GTC ATC ATA AAA AAG CGC CAG ATA ACT CCG GAT GTA TAT AAG G
< 2040

1990 2000 2010 2020 2030




TC ACT CCA GTG ATG AAC ACA CAT CCG TCC CAA TCA GAA GCC GTA TCA GAT GTT TGG TCT C
< 2100

2050 2060 2070 2080 2090




TC TCA AAG ACA TCC ATG ACT TTC CAA CCC AAG AAA GCA AGT CTT CAG CCT CTC ACC ATA T
< 2160

2110 2120 2130 2140 2150




CC TTG GAT GAA TTG TTC TCATCT AGA GGA GAA TTC ATC TCT GTC GGA GGT AAC GGA CGA A
< 2220

2170 2180 2190 2200 2210




TG TCT CAT AAA GAG GCC ATC CTG CTC GGT CTG AGG TAC AAA AAG TTG TAC AAT CAG GCG A
< 2280

2230 2240 2250 2260 2270




GA GTC AAA TAT TCT CTG TAG ACT AGT ATG AAA AAA AGT AAC AGA TAT CAC AAT CTA AGT G
< 2340

2290 2300 2310 2320 2330




TT ATC CCA ATC CAT TCA TCA TGA GTT CCT TAA AGA AGA TTC TCG GTC TGA AGG GGA AAG G
< 2400

2350 2360 2370 2380 2390




TA AGA AAT CTA AGA AAT TAG GGA TCG CAC CAC CCC CTT ATG AAG AGG ACA CTA ACA TGG A
< 2460

2410 2420 2430 2440 2450




GT ATG CTC CGA GCG CTC CAA TTG ACA AAT CCT ATT TTG GAG TTG ACG AGA TGG ACA CTC A
< 2520

2470 2480 2490 2500 2510




TG ATC CGA ATC AAT TAA GAT ATG AGA AAT TCT TCT TTA CAG TGA AAA TGA CGG TTA GAT C
< 2580

2530 2540 2550 2560 2570




TA ATC GTC CGT TCA GAA CAT ACT CAG ATG TGG CAG CCG CTG TAT CCC ATT GGG ATC ACA T
< 2640

2590 2600 2610 2620 2630




GT ACA TCG GAA TGG CAG GGA AAC GTC CCT TCT ACA AGA TCT TGG CTT TTT TGG GTT CTT C
< 2700

2650 2660 2670 2680 2690




>M


|


TA ATC TAA AGG CCA CTC CAG CGG TAT TGG CAG ATC AAG GTC AAC CAG AGT ATC ATG CTC A
< 2760

2710 2720 2730 2740 2750




CT GTG AAG GCA GGG CTT ATT TGC CAC ACA GAA TGG GGA AGA CCC CTC CCA TGC TCA ATG T
< 2820

2770 2780 2790 2800 2810




AC CAG AGC ACT TCA GAA GAC CAT TCA ATA TAG GTC TTT ACA AGG GAA CGA TTG AGC TCA C
< 2880

2830 2840 2850 2860 2870




AA TGA CCA TCT ACG ATG ATG AGT CAC TGG AAG CAG CTC CTA TGA TCT GGG ATC ATT TCA A
< 2940

2890 2900 2910 2920 2930




TT CTT CCA AAT TTT CTG ATT TCA GAG AGA AGG CCT TAA TGT TTG GCC TGA TTG TCG AGA A
< 3000

2950 2960 2970 2980 2990




AA AGG CAT CTG GAG CTT GGG TCC TGG ATT CTG TCA GCC ACT TCA AAT GAG CTA GTC TAG C
< 3060

3010 3020 3030 3040 3050




TT CCA GCT TCT GAA CAA TCC CCG GTT TAC TCA GTC TCT CCT AAT TCC AGC CTT TCG AAC A
< 3120

3070 3080 3090 3100 3110




AC TAA TAT CCT GTC TTC TCT ATC CCT ATG AAA AAA ACT AAC AGA GAT CGA TCT GTT TCC T
< 3180

3130 3140 3150 3160 3170




TG ACA CCA GGA GCC ACC ATG AAG TGG CTT TTG TAC TTA GCT TTT TTA TTC ATC GGG GTG A
< 3240

M K C L L Y L A F L F I G V N


3190 3200 3210 3220 3230




AT TGC AAG GCT AGC GCA GAG AAT TTG TGG GTA ACA GTC TAC TAT GGA GTC CCT GTA TGG A
< 3300

C K A S A E N L W V T V Y Y G V P V W K


3250 3260 3270 3280 3290




AG GAT GCA GAG ACA ACA TTG TTC TGT GCT AGT GAC GCA AAG GCT TAC GAG ACG GAG AAG C
< 3360

D A E T T L F C A S D A K A Y E T E K H


3310 3320 3330 3340 3350




AC AAT GTG TGG GCA ACT CAC GCA TGT GTC CCA ACC GAT CCA AAT CCT CAA GAG ATT CAT C
< 3420

N V W A T H A C V P T D P N P Q E I H L


3370 3380 3390 3400 3410




TA GAG AAT GTG ACT GAA GAA TTC AAT ATG TGG AAG AAT AAT ATG GTA GAG CAA ATG CAT A
< 3480

E N V T E E F N M W K N N M V E Q M H T


3430 3440 3450 3460 3470




CA GAT ATC ATT AGT TTA TGG GAC CAG TCA CTT AAA CCC TGC GTT AAA TTG ACG CCT CTA T
< 3540

D I I S L W D Q S L K P C V K L T P L C


3490 3500 3510 3520 3530




GT GTG ACA CTT CAA TGT ACT AAT GTT ACA AAC AAC ATA ACA GAT GAT ATG AGA GGA GAA C
< 3600

V T L Q C T N V T N N I T D D M R G E L


3550 3560 3570 3580 3590




TG AAG AAC TGT AGT TTC AAC ATG ACG ACA GAG TTG CGT GAC AAG AAA CAG AAA GTG TAT T
< 3660

K N C S F N M T T E L R D K K Q K V Y S


3610 3620 3630 3640 3650




CA CTA TTC TAT CGG TTG GAT GTA GTA CAG ATA AAT GAG AAT CAA GGA AAC AGG TCC AAC A
< 3720

L F Y R L D V V Q I N E N Q G N R S N N


3670 3680 3690 3700 3710




AC TCT AAC AAA GAG TAC AGA CTT ATT AAT TGC AAT ACC AGT GCT ATC ACG CAA GCC TGC C
< 3780

S N K E Y R L I N C N T S A I T Q A C P


3730 3740 3750 3760 3770




CA AAG GTT TCA TTT GAA CCA ATA CCT ATT CAT TAT TGT GCA CCT GCT GGA TTC GCC ATC C
< 3840

K V S F E P I P I H Y C A P A G F A I L


3790 3800 3810 3820 3830




TC AAA TGT AAA GAC AAG AAG TTC AAT GGA ACA GGA CCC TGC CCA TCA GTT TCA ACC GTT C
< 3900

K C K D K K F N G T G P C P S V S T V Q


3850 3860 3870 3880 3890




AG TGC ACC CAC GGA ATC AAG CCT GTA GTT AGT ACT CAA TTA TTG TTA AAT GGG AGC TTA G
< 3960

C T H G I K P V V S T Q L L L N G S L A


3910 3920 3930 3940 3950




CT GAA GAA GAA GTT ATG ATT AGA TCA GAG AAT ATT ACC AAT AAT GCG AAG AAC ATC TTG G
< 4020

E E E V M I R S E N I T N N A K N I L V


3970 3980 3990 4000 4010




TT CAA TTC AAT ACT CCA GTC CAG ATC AAT TGC ACA AGG CCT AAT AAT AAT ACC AGA AAG A
< 4080

Q F N T P V Q I N C T R P N N N T R K S


4030 4040 4050 4060 4070




GT ATA AGA ATT GGG CCA GGA CAG GCA TTC TAT GCA ACA GGA GAT ATA ATC GGA GAC ATT C
< 4140

I R I G P G Q A F Y A T G D I I G D I R


4090 4100 4110 4120 4130




GA CAA GCG CAC TGC ACT GTT TCT AAG GCC ACT TCG AAT GAA ACA TTG GGT AAA GTT GTA A
< 4200

Q A H C T V S K A T W N E T L G K V V K


4150 4160 4170 4180 4190




AG CAA CTT CGG AAG CAT TTC GGA AAT AAC ACA ATT ATT AGA TTT GCG AAC TCA TCT GGA G
< 4260

Q L R K H F G N N T I I R F A N S S G G


4210 4220 4230 4240 4250




>Env.BG505 immunogen


|


GG GAT CTG GAA GAG ACA ACA CAC TCT TTC AAT TGC GGT GGC GAG TTC TTC TAT TGT AAT A
< 4320

D L E V T T N S F N C G G E F F Y C N T


4270 4280 4290 4300 4310




CA AGT GGA TTA TTT AAC TCT ACT TGG ATT TCA AAT ACC TCA GTC CAA GGA TCT AAT TCA A
< 4380

S G L F N S T W I S N T S V Q G S N S T


4330 4340 4350 4360 4370




CA GGG TCT AAC GAT TCT ATA ACA TTA CCT TGC CGT ATA AAG CAA ATT ATT AAT ATG TGG C
< 4440

G S N D S I T L P C R I K Q I I N M W Q


4390 4400 4410 4420 4430




AA AGA ATC GGG CAA GCG ATG TAT GCT CCA CCT ATT CAA GGC GTG ATT CGT TGC GTT TCA A
< 4500

R I G Q A M Y A P P I Q G V I K C V S N


4450 4460 4470 4480 4490




AC ATA ACA GGG TTG ATC CTG ACC AGG GAT GGA GGC TCT ACC AAT TCC ACC ACC GAG ACC T
< 4560

I T G L I L T R D G G S T N S T T E T F


4510 4520 4530 4540 4550




TC CGT CCC GGT GGC GGA GAT ATG CGG GAT AAC TGG AGA TCA GAG CTC TAT AAG TAT AAG G
< 4620

R P G G G D M R D N W R S E L Y K Y K V


4570 4580 4590 4600 4610




TT GTG AAG ATT GAA CCT CTT GGA GTT GCC CCT ACA AGA GCA AAG AGA AGG GTG GTT GGC C
< 4680

V K I E P L G V A P T R A K R R V V G R


4630 4640 4650 4660 4670




GA GAG AAG AGA GCA GTT GGC ATC GGT GCT GTC TTT CTC GGA TTT CTT GGA GCA GCT GGA T
< 4740

E K R A V G I G A V F L G F L G A A G S


4690 4700 4710 4720 4730




CC ACT ATG GGA GCA GCA TCA ATG ACA CTA ACA GTG CAG GCT AGA AAT TTG CTT AGC GGA A
< 4800

T M G A A S M T L T V Q A R N L L S G I


4750 4760 4770 4780 4790




TC GTT CAG CAG CAG AGC AAT TTA CTA AGA GCA ATT GAA GCA CAG CAA CAT CTC TTA AAG T
< 4860

V Q Q Q S N L L R A I E A Q Q H L L K L


4810 4820 4830 4840 4850




TG ACG GTG TGG GGC ATT AAA CAA CTA CAA GCG AGA GTG CTT GCC GTC GAA AGA TAT TTG C
< 4920

T V N G I K Q L Q A R V L A V E R Y L R


4870 4880 4890 4900 4910




GA GAC CAA CAG CTA TTG GGT ATT TGG GGT TGT TCT GCG AAA TTA ATT TGC ACA ACA AAT G
< 4980

D Q Q L L G I W G C S G K L I C T T N V


4930 4940 4950 4960 4970




TT CCA TGG AAC TCC TCC TGG AGT AAT AGG AAT TTA AGT GAG ATA TGG GAC AAC ATG ACA T
< 5040

P W N S S W S N R N L S E I W D N M T W


4990 5000 5010 5020 5030




GG TTG CAG TGG GAC AAG GAA ATC TCA AAT TAT ACA CAG ATA ATC TAT GGA TTA TTA GAA G
< 5100

L Q W D K E I S N Y T Q I I Y G L L E E


5050 5060 5070 5080 5090




AG TCT CAG AAT CAG CAA GAG AAG AAT GAA CAG GAT TTG CTT GCA TTG GAT AAG TGG GCT T
< 5160

S Q N Q Q E K N E Q D L L A L D K W A S


5110 5120 5130 5140 5150




CT CTA TGG AAC TGG TTC GAT ATT AGT AAT TGG CTC TGG TAT ATT AAG AGC TCT ATT GCC T
< 5220

L W N W F D I S N W L W Y I K S S I A S


5170 5180 5190 5200 5210




CT TTT TTC TTT ATC ATA GGG TTA ATC ATT GGA CTA TTC TTG GTT CTC CGA GTT GGT ATT T
< 5280

F F F I I G L I I G L F L V L R V G I Y


5230 5240 5250 5260 5270




AT CTT TGC ATT AAA TTA AAG CAC ACC AAG AAA AGA CAG ATT TAT ACA GAC ATA GAG ATG A
< 5340

L C I K L K H T K K R Q I Y T D I E M N


5290 5300 5310 5320 5330




AC CGA CTT GGA AAG TAA AGC TCA AAT CCT GCA CAA CAG ATT CTT CAT GTT TGA ACC AAA T
< 5400

R L G K *


5350 5360 5370 5380 5390




CA ACT TGT GAT ATC ATG CTC AAA GAG GCC TTA ATT AAA TTT TAA TTT TTA ATT TTT ATG A
< 5460

5410 5420 5430 5440 5450




AA AAA ACT AAC AGC AAT CAT GGA AGT CCA CGA TTT TGA GAC CGA CGA GTT CAA TGA TTT C
< 5520

5470 5480 5490 5500 5510




AA TGA AGA TGA CTA TGC CAC AAG AGA ATT CCT GAA TCC CGA TGA GCG CAT GAC GTA CTT G
< 5580

5530 5540 5550 5560 5570




AA TCA TGC TGA TTA CAA TTT GAA TTC TCC TCT AAT TAG TGA TGA TAT TGA CAA TTT GAT C
< 5640

5590 5600 5610 5620 5630




AG GAA ATT CAA TTC TCT TCC GAT TCC CTC GAT GTG GGA TAG TAA GAA CTG GGA TGG AGT T
< 5700

5650 5660 5670 5680 5690




CT TGA GAT GTT AAC ATC ATG TCA AGC CAA TCC CAT CTC AAC ATC TCA GAT GCA TAA ATG G
< 5760

5710 5720 5730 5740 5750




AT GGG AAG TTG GTT AAT GTC TGA TAA TCA TGA TGC CAG TCA AGG GTA TAG TTT TTT ACA T
< 5820

5770 5780 5790 5800 5810




GA AGT GGA CAA AGA GGC AGA AAT AAC ATT TGA CGT GGT GGA GAC CTT CAT CCG CGG CTG G
< 5880

5830 5840 5850 5860 5870




GG CAA CAA ACC AAT TGA ATA CAT CAA AAA GGA AAG ATG GAC TGA CTC ATT CAA AAT TCT C
< 5940

5890 5900 5910 5920 5930




GC TTA TTT GTG TCA AAA GTT TTT GGA CTT ACA CAA GTT GAC ATT AAT CTT AAA TGC TGT C
< 6000

5950 5960 5970 5980 5990




TC TGA GGT GGA ATT GCT CAA CTT GGC GAG GAC TTT CAA AGG CAA AGT CAG AAG AAG TTC T
< 6060

6010 6020 6030 6040 6050




CA TGG AAC GAA CAT ATG CAG GCT TAG GGT TCC CAG CTT GGG TCC TAC TTT TAT TTC AGA A
< 6120

6070 6080 6090 6100 6110




GG ATG GGC TTA CTT CAA GAA ACT TGA TAT TCT AAT GGA CCG AAA CTT TCT GTT AAT GGT C
< 6180

6130 6140 6150 6160 6170




AA AGA TGT GAT TAT AGG GAG GAT GCA AAC GGT GCT ATC CAT GGT ATG TAG AAT AGA CAA C
< 6240

6190 6200 6210 6220 6230




CT GTT CTC AGA GCA AGA CAT CTT CTC CCT TCT AAA TAT CTA CAG AAT TGG AGA TAA AAT T
< 6300

6250 6260 6270 6280 6290




GT GGA GAG GCA GGG AAA TTT TTC TTA TGA CTT GAT TAA AAT GGT GGA ACC GAT ATG CAA C
< 6360

6310 6320 6330 6340 6350




TT GAA GCT GAT GAA ATT AGC AAG AGA ATC AAG GCC TTT AGT CCC ACA ATT CCC TCA TTT T
< 6420

6370 6380 6390 6400 6410




GA AAA TCA TAT CAA GAC TTC TGT TGA TGA AGG GGC AAA AAT TGA CCG AGG TAT AAG ATT C
< 6480

6430 6440 6450 6460 6470




CT CCA TGA TCA GAT AAT GAG TGT GAA AAC AGT GGA TCT CAC ACT GGT GAT TTA TGG ATC G
< 6540

6490 6500 6510 6520 6530




TT CAG ACA TTG GGG TCA TCC TTT TAT AGA TTA TTA CGC TGG ACT AGA AAA ATT ACA TTC C
< 6600

6550 6560 6570 6580 6590




CA AGT AAC CAT GAA GAA AGA TAT TGA TGT GTC ATA TGC AAA AGC ACT TGC AAG TGA TTT A
< 6660

6610 6620 6630 6640 6650




GC TCG GAT TGT TCT ATT TCA ACA GTT CAA TGA TCA TAA AAA GTG GTT CGT GAA TGG AGA C
< 6720

6670 6680 6690 6700 6710




TT GCT CCC TCA TGA TCA TCC CTT TAA AAG TCA TGT TAA AGA AAA TAC ATG GCC TAC AGC T
< 6780

6730 6740 6750 6760 6770




GC TCA AGT TCA AGA TTT TGG AGA TAA ATG GCA TGA ACT TCC GCT GAT TAA ATG TTT TGA A
< 6840

6790 6800 6810 6820 6830




AT ACC CGA CTT ACT AGA CCC ATC GAT AAT ATA CTC TGA CAA AAG TCA TTC AAT GAA TAG G
< 6900

6850 6860 6870 6880 6890




TC AGA GGT GTT GAA ACA TGT CCG AAT GAA TCC GAA CAC TCC TAT CCC TAG TAA AAA GGT G
< 6960

6910 6920 6930 6940 6950




TT GCA GAC TAT GTT GGA CAC AAA GGC TAC CAA TTG GAA AGA ATT TCT TAA AGA GAT TGA T
< 7020

6970 6980 6990 7000 7010




GA GAA GGG CTT AGA TGA TGA TGA TCT AAT TAT TGG TCT TAA AGG AAA GGA GAG GGA ACT G
< 7080

7030 7040 7050 7060 7070




AA GTT GGC AGG TAG ATT TTT CTC CCT AAT GTC TTG GAA ATT GCG AGA ATA CTT TGT AAT T
< 7140

7090 7100 7110 7120 7130




AC CGA ATA TTT GAT AAA GAC TCA TTT CGT CCC TAT GTT TAA AGG CCT GAC AAT GGC GGA C
< 7200

7150 7160 7170 7180 7190




GA TCT AAC TGC AGT CAT TAA AAA GAT GTT AGA TTC CTC ATC CGG CCA AGG ATT GAA GTC A
< 7260

7210 7220 7230 7240 7250




TA TGA GGC AAT TTG CAT AGC CAA TCA CAT TGA TTA CGA AAA ATG GAA TAA CCA CCA AAG G
< 7320

7270 7280 7290 7300 7310




AA GTT ATC AAA CGG CCC AGT GTT CCG AGT TAT GGG CCA GTT CTT AGG TTA TCC ATC CTT A
< 7380

7330 7340 7350 7360 7370




AT CGA GAG AAC TCA TGA ATT TTT TGA GAA AAG TCT TAT ATA CTA CAA TGG AAG ACC AGA C
< 7440

7390 7400 7410 7420 7430




TT GAT GCG TGT TCA CAA CAA CAC ACT GAT CAA TTC AAC CTC CCA ACG AGT TTG TTG GCA A
< 7500

7450 7460 7470 7480 7490




GG ACA AGA GGG TGG ACT GGA AGG TCT ACG GCA AAA AGG ATG GAG TAT CCT CAA TCT ACT G
< 7560

7510 7520 7530 7540 7550




GT TAT TCA AAG AGA GGC TAA AAT CAG AAA CAC TGC TGT CAA AGT CTT GGC ACA AGG TGA T
< 7620

7570 7580 7590 7600 7610




AA TCA AGT TAT TTG CAC ACA GTA TAA AAC GAA GAA ATC GAG AAA CGT TGT AGA ATT ACA G
< 7680

7630 7640 7650 7660 7670




GG TGC TCT CAA TCA AAT GGT TTC TAA TAA TGA GAA AAT TAT GAC TGC AAT CAA AAT AGG G
< 7740

7690 7700 7710 7720 7730




AC AGG GAA GTT AGG ACT TTT GAT AAA TGA CGA TGA GAC TAT GCA ATC TGC AGA TTA CTT G
< 7800

7750 7760 7770 7780 7790




AA TTA TGG AAA AAT ACC GAT TTT CCG TGG AGT GAT TAG AGG GTT AGA GAC CAA GAG ATG G
< 7860

7810 7820 7830 7840 7850




TC ACG AGT GAC TTG TGT CAC CAA TGA CCA AAT ACC CAC TTG TGC TAA TAT AAT GAG CTC A
< 7920

7870 7880 7890 7900 7910




GT TTC CAC AAA TGC TCT CAC CGT AGC TCA TTT TGC TGA GAA CCC AAT CAA TGC CAT GAT A
< 7980

7930 7940 7950 7960 7970




CA GTA CAA TTA TTT TGG GAC ATT TGC TAG ACT CTT GTT GAT GAT GCA TGA TCC TGC TCT T
< 8040

7990 8000 8010 8020 8030




CG TCA ATC ATT GTA TGA AGT TCA AGA TAA GAT ACC GGG CTT GCA CAG TTC TAC TTT CAA A
< 8100

8050 8060 8070 8080 8090




TA CGC CAT GTT GTA TTT GGA CCC TTC CAT TGG AGG AGT GTC GGG CAT GTC TTT GTC CAG G
< 8160

8110 8120 8130 8140 8150




TT TTT GAT TAG AGC CTT CCC AGA TCC CGT AAC AGA AAG TCT CTC ATT CTG GAG ATT CAT C
< 8220

8170 8180 8190 8200 8210




CA TGT ACA TGC TCG AAG TGA GCA TCT GAA GGA GAT GAG TGC AGT ATT TGG AAA CCC CGA G
< 8280

8230 8240 8250 8260 8270




AT AGC CAA GTT CCG AAT AAC TCA CAT AGA CAA GCT AGT AGA AGA TCC AAC CTC TCT GAA C
< 8340

8290 8300 8310 8320 8330




AT CGC TAT GGG AAT GAG TCC AGC GAA CTT GTT AAA GAC TGA GGT TAA AAA ATG CTT AAT C
< 8400

8350 8360 8370 8380 8390




GA ATC AAG ACA AAC CAT CAG GAA CCA GGT GAT TAA GGA TGC AAC CAT ATA TTT GTA TCA T
< 8460

8410 8420 8430 8440 8450




GA AGA GGA TCG GCT CAG AAG TTT CTT ATG GTC AAT AAA TCC TCT GTT CCC TAG ATT TTT A
< 8520

8470 8480 8490 8500 8510




AG TGA ATT CAA ATC AGG CAC TTT TTT GGG AGT CGC AGA CGG GCT CAT CAG TCT ATT TCA A
< 8580

8530 8540 8550 8560 8570




AA TTC TCG TAC TAT TCG GAA CTC CTT TAA GAA AAA GTA TCA TAG GGA ATT GGA TGA TTT G
< 8640

8590 8600 8610 8620 8630




>L


|


AT TGT GAG GAG TGA GGT ATC CTC TTT GAC ACA TTT AGG GAA ACT TCA TTT GAG AAG GGG A
< 8700

8650 8660 8670 8680 8690




TC ATG TAA AAT GTG GAC ATG TTC AGC TAC TCA TGC TGA CAC ATT AAG ATA CAA ATC CTG G
< 8760

8710 8720 8730 8740 8750




GG CCG TAC AGT TAT TGG GAC AAC TGT ACC CCA TCC ATT AGA AAT GTT GGG TCC ACA ACA T
< 8820

8770 8780 8790 8800 8810




CG AAA AGA GAC TCC TTG TGC ACC ATG TAA CAC ATC AGG GTT CAA TTA TGT TTC TGT GCA T
< 8880

8830 8840 8850 8860 8870




TG TCC AGA CGG GAT CCA TGA CGT CTT TAG TTC ACG GGG ACC ATT GCC TGC TTA TCT AGG G
< 8940

8890 8900 8910 8920 8930




TC TAA AAC ATC TGA ATC TAC ATC TAT TTT GCA GCC TTG GGA AAG GGA AAG CAA AGT CCC A
< 9000

8950 8960 8970 8980 8990




CT GAT TAA AAG AGC TAC ACG TCT TAG AGA TGC TAT CTC TTG GTT TGT TGA ACC CGA CTC T
< 9060

9010 9020 9030 9040 9050




AA ACT AGC AAT GAC TAT ACT TTC TAA CAT CCA CTC TTT AAC AG G CGA AGA AT GAC CAA A
< 9120

9070 9080 9090 9100 9110




AG GCA GCA TGG GTT CAA AAG AAC AGG GTC TGC CCT TCA TAG GTT TTC GAC ATC TCG GAT G
< 9180

9130 9140 9150 9160 9170




AG CCA TGG TGG GTT CGC ATC TCA GAG CAC TGC AGC ATT GAC CAG GTT GAT GGC AAC TAC A
< 9240

9190 9200 9210 9220 9230




GA CAC CAT GAG GGA TCT GGG AGA TCA GAA TTT CGA CTT TTT ATT CCA AGC AAC GTT GCT C
< 9300

9250 9260 9270 9280 9290




TA TGC TCA AAT TAC CAC CAC TGT TGC AAG AGA CGG ATG GAT CAC CAG TTG TAC AGA TCA T
< 9360

9310 9320 9330 9340 9350




TA TCA TAT TGC CTG TAA GTC CTG TTT GAG ACC CAT AGA AGA GAT CAC CCT GGA CTC AAG T
< 9420

9370 9380 9390 9400 9410




AT GGA CTA CAC GCC CCC AGA TGT ATC CCA TGT GCT GAA GAC ATG GAG GAA TGG GGA AGG T
< 9480

9430 9440 9450 9460 9470




TC GTG GGG ACA AGA GAT AAA ACA GAT CTA TCC TTT AGA AGG GAA TTG GAA GAA TTT AGC A
< 9540

9490 9500 9510 9520 9530




CC TGC TGA GCA ATC CTA TCA AGT CGG CAG ATG TAT AGG TTT TCT ATA TGG AGA CTT GGC G
< 9600

9550 9560 9570 9580 9590




TA TAG AAA ATC TAC TCA TGC CGA GGA CAG TTC TCT ATT TCC TCT ATC TAT ACA AGG TCG T
< 9660

9610 9620 9630 9640 9650




AT TAG AGG TCG AGG TTT CTT AAA AGG GTT GCT AGA CGG ATT AAT GAG AGC AAG TTG CTG C
< 9720

9670 9680 9690 9700 9710




CA AGT AAT ACA CCG GAG AAG TCT GGC TCA TTT GAA GAG GCC GGC CAA CGC AGT GTA CGG A
< 9780

9730 9740 9750 9760 9770




GG TTT GAT TTA CTT GAT TGA TAA ATT GAG TGT ATC ACC TCC ATT CCT TTC TCT TAC TAG A
< 9840

9790 9800 9810 9820 9830




TC AGG ACC TAT TAG AGA CGA ATT AGA AAC GAT TCC CCA CAA GAT CCC AAC CTC CTA TCC G
< 9900

9850 9860 9870 9880 9890




AC AAG CAA CCG TGA TAT GGG GGT GAT TGT CAG AAA TTA CTT CAA ATA CCA ATG CCG TCT A
< 9960

9910 9920 9930 9940 9950




AT TGA AAA GGG AAA ATA CAG ATC ACA TTA TTC ACA ATT ATG GTT ATT CTC AGA TGT CTT A
< 10020

9970 9980 9990 10000 10010




TC CAT AGA CTT CAT TGG ACC ATT CTC TAT TTC CAC CAC CCT CTT GCA AAT CCT ATA CAA G
< 10080

10030 10040 10050 10060 10070




CC ATT TTT ATC TGG GAA AGA TAA GAA TGA GTT GAG AGA GCT GGC AAA TCT TTC TTC ATT G
< 10140

10090 10100 10110 10120 10130




CT AAG ATC AGG AGA GGG GTG GGA AGA CAT ACA TGT GAA ATT CTT CAC CAA GGA CAT ATT A
< 10200

10150 10160 10170 10180 10190




TT GTG TCC AGA GGA AAT CAG ACA TGC TTG CAA GTT CGG GAT TGC TAA GGA TAA TAA TAA A
< 10260

10210 10220 10230 10240 10250




GA CAT GAG CTA TCC CCC TTG GGG AAG GGA ATC CAG AGG GAC AAT TAC AAC AAT CCC TGT T
< 10320

10270 10280 10290 10300 10310




TA TTA TAC GAC CAC CCC TTA CCC AAA GAT GCT AGA GAT GCC TCC AAG AAT CCA AAA TCC C
< 10380

10330 10340 10350 10360 10370




CT GCT GTC CGG AAT CAG GTT GGG CCA ATT ACC AAC TGG CGC TCA TTA TAA AAT TCG GAG T
< 10440

10390 10400 10410 10420 10430




AT ATT ACA TGG AAT GGG AAT CCA TTA CAG GGA CTT CTT GAG TTG TGG AGA CGG CTC CGG A
< 10500

10450 10460 10470 10480 10490




GG GAT GAC TGC TGC ATT ACT ACG AGA AAA TGT GCA TAG CAG AGG AAT ATT CAA TAG TCT G
< 10560

10510 10520 10530 10540 10550




TT AGA ATT ATC AGG GTC AGT CAT GCG AGG CGC CTC TCC TGA GCC CCC CAG TGC CCT AGA A
< 10620

10570 10580 10590 10600 10610




AC TTT AGG AGG AGA TAA ATC GAG ATG TGT AAA TGG TGA AAC ATG TTG GGA ATA TCC ATC T
< 10680

10630 10640 10650 10660 10670




GA CTT ATG TGA CCC AAG GAC TTG GGA CTA TTT CCT CCG ACT CAA AGC AGG CTT GGG GCT T
< 10740

10690 10700 10710 10720 10730




CA AAT TGA TTT AAT TGT AAT GGA TAT GGA AGT TCG GGA TTC TTC TAC TAG CCT GAA AAT T
< 10800

10750 10760 10770 10780 10790




GA GAC GAA TGT TAG AAA TTA TGT GCA CCG GAT TTT GGA TGA GCA AGG AGT TTT AAT CTA C
< 10860

10810 10820 10830 10840 10850




AA GAC TTA TGG AAC ATA TAT TTG TGA GAG CGA AAA GAA TGC AGT AAC AAT CCT TGG TCC C
< 10920

10870 10880 10890 10900 10910




AT GTT CAA GAC GGT CGA CTT AGT TCA AAC AGA ATT TAG TAG TTC TCA AAC GTC TGA AGT A
< 10980

10930 10940 10950 10960 10970




TA TAT GGT ATG TAA AGG TTT GAA GAA ATT AAT CGA TGA ACC CAA TCC CGA TTG GTC TTC C
< 11040

10990 11000 11010 11020 11030




AT CAA TGA ATC CTG GAA AAA CCT GTA CGC ATT CCA GTC ATC AGA ACA GGA ATT TGC CAG A
< 11100

11050 11060 11070 11080 11090




GC AAA GAA GGT TAG TAC ATA CTT TAC CTT GAC AGG TAT TCC CTC CCA ATT CAT TCC TGA T
< 11160

11110 11120 11130 11140 11150




CC TTT TGT AAA CAT TGA GAC TAT GCT ACA AAT ATT CGG AGT ACC CAC GGG TGT GTC TCA T
< 11220

11170 11180 11190 11200 11210




GC GGC TGC CTT AAA ATC ATC TGA TAG ACC TGC AGA TTT ATT GAC CAT TAG CCT TTT TTA T
< 11280

11230 11240 11250 11260 11270




AT GGC GAT TAT ATC GTA TTA TAA CAT CAA TCA TAT CAG AGT AGG ACC GAT ACC TCC GAA C
< 11340

11290 11300 11310 11320 11330




CC CCC ATC AGA TGG AAT TGC ACA AAA TGT GGG GAT CGC TAT AAC TGG TAT AAG CTT TTG G
< 11400

11350 11360 11370 11380 11390




CT GAG TTT GAT GGA GAA AGA CAT TCC ACT ATA TCA ACA GTG TTT AGC AGT TAT CCA GCA A
< 11460

11410 11420 11430 11440 11450




TC ATT CCC GAT TAG GTG GGA GGC TGT TTC AGT AAA AGG AGG ATA CAA GCA GAA GTG GAG T
< 11520

11470 11480 11490 11500 11510




AC TAG AGG TGA TGG GCT CCC AAA AGA TAC CCG AAT TTC AGA CTC CTT GGC CCC AAT CGG G
< 11580

11530 11540 11550 11560 11570




AA CTG GAT CAG ATC TCT GGA ATT GGT CCG AAA CCA AGT TCG TCT AAA TCC ATT CAA TGA G
< 11640

11590 11600 11610 11620 11630




AT CTT GTT CAA TCA GCT ATG TCG TAC AGT GGA TAA TCA TTT GAA ATG GTC AAA TTT GCG A
< 11700

11650 11660 11670 11680 11690




AA AAA CAC AGG AAT GAT TGA ATG GAT CAA TAG ACG AAT TTC AAA AGA AGA CCG GTC TAT A
< 11760

11710 11720 11730 11740 11750




CT GAT GTT GAA GAG TGA CCT ACA CGA GGA AAA CTC TTG GAG AGA TTA AAA AAT CAT GAG G
< 11820

11770 11780 11790 11800 11810




>VSV Trailer


|


AG ACT CCA AAC TTT AAG TAT GAA AAA AAC TTT GAT CCT TAA GAC CCT CTT GTG GTT TTT A
< 11880

11830 11840 11850 11860 11870




TT TTT TAT CTG GTT TTG TGG TCT TCG Tgg ccg gca tgg tcc cag cct cct cgc tgg cgc c
< 11940

11890 11900 11910 11920 11930




>Hepatitis Delta Virus Ribozyme


|


gg ctg ggc aac att ccg agg gga ccg tcc cct cgg taa tgg cga atg gga cct gct aac a
< 12000

11950 11960 11970 11980 11990




aa gcc cga aag gaa gct gag ttg gct gct gcc acc gct gag caa taa cta gca taa ccc c
< 12060

12010 12020 12030 12040 12050




tt ggg gcc tct aaa cgg gtc ttg agg ggt ttt ttg ctg aaa gga gga act ata tcc gga t
< 12120

12070 12080 12090 12100 12110




>T7 Terminators


|


gc ggc cga tcc ggc tgc taa caa agc ccg aaa gga agc tga gtt ggc tgc tgc cac cgc t
< 12180

12130 12140 12150 12160 12170




ga gca ata act agc ata acc cct tgg ggc ctc taa acg ggt ctt gag ggg ttt ttt gct g
< 12240

12190 12200 12210 12220 12230




aa agg agg aac tat atc cgg gtt aac ctg cat taa tga atc ggc caa cgc gcg ggg aga g
< 12300

12250 12260 12270 12280 12290




gc ggt ttg cgt att ggg cgc tct tcc gct tcc tcg ctc act gac tcg ctg cgc tcg gtc g
< 12360

12310 12320 12330 12340 12350




tt cgg ctg cgg cga gcg gta tca gct cac tca aag gcg gta ata cgg tta tcc aca gaa t
< 12420

12370 12380 12390 12400 12410




ca ggg gat aac gca gga aag aac atg tga gca aaa ggc cag caa aag gcc agg aac cgt a
< 12480

12430 12440 12450 12460 12470




aa aag gcc gcg ttg ctg gcg ttt ttc cat agg ctc cgc ccc cct gac gag cat cac aaa c
< 12540

12490 12500 12510 12520 12530




at cga cgc tca agt cag agg tgg cga aac ccg aca gga cta taa aga tac cag gcg ttt c
< 12600

12550 12560 12570 12580 12590




cc cct gga agc tcc ctc gtg cgc tct cct gtt ccg acc ctg ccg ctt acc gga tac ctg t
< 12660

12610 12620 12630 12640 12650




cc gcc ttt ctc cct tcg gga gac gtg gcg ctt tct caa tgc tca cgc tgt agg tat ctc a
< 12720

12670 12680 12690 12700 12710




gt tcg gtg tag gtc gtt cgc tcc aag ctg ggc tgt gtg cac gaa ccc ccc gtt cag ccc g
< 12780

12730 12740 12750 12760 12770




ac cgc tgc gcc tta tcc ggt aac tat cgt ctt gag tcc aac ccg gta aga cac gac tta t
< 12840

12790 132800 12810 12820 12830




cg cca ctg gca gca gcc act ggt aac agg att agc aga gcg agg tat gta ggc ggt gct a
< 12900

12850 12860 12870 12880 12890




ca gag ttc ttg aag tgg tgg cct aac tac ggc tac act aga agg aca gta ttt ggt atc t
< 12960

12910 12920 12930 12940 12950




gc gct ctg ctg aag cca gtt acc ttc gga aaa aga gtt ggt agc tct tga tcc ggc aaa c
< 13020

12970 12980 12990 13000 13010




aa acc acc gct ggt agc ggt ggt ttt ttt gtt tgc aag cag cag att acg cgc aga aaa a
< 13080

13030 13040 13050 13060 13070




aa gga tct caa gaa gat cct ttg atc ttt tct acg ggg tct gac gct cag tgg aac gaa a
< 13140

13090 13100 13110 13120 13130




ac tca cgt taa ggg att ttg gtc atg aga tta tca aaa agg atc ttc acc tag atc ctt t
< 13200

13150 13160 13170 13180 13190




>pSP72


|


ta aat taa aaa tga agt ttt aaa tca atc taa agt ata tat gag taa act tgg tct gac a
< 13260

13210 13220 13230 13240 13250




gt tac caa tgc tta atc agt gag gca cct atc tca gcg atc tgt cta ttt cgt tca tcc a
< 13320

13270 13280 13290 13300 13310




ta gtt gcc tga ctc ccc gtc gtg tag ata act acg ata cgg gag ggc tta cca tct ggc c
< 13380

13330 13340 13350 13360 13370




cc agt gct gca atg ata ccg cga gac cca cgc tca ccg gct cca gat tta tca gca ata a
< 13440

13390 13400 13410 13420 13430




ac cag cca gcc gga agg gcc gag cgc aga agt ggt cct gca act tta tcc gcc tcc atc c
< 13500

13450 13460 13470 13480 13490




ag tct att aat tgt tgc cgg gaa gct aga gta agt agt tcg cca gtt aat agt ttg cgc a
< 13560

13510 13520 13530 13540 13550




ac gtt gtt gcc att gct aca ggc atc gtg gtg tca cgc tcg tcg ttt ggt atg gct tca t
< 13620

13570 13580 13590 13600 13610




tc agc tcc ggt tcc caa cga tca agg cga gtt aca tga tcc ccc atg ttg tgc aaa aaa g
< 13680

13630 13640 13650 13660 13670




cg gtt agc tcc ttc ggt cct ccg atc gtt gtc aga agt aag ttg gcc gca gtg tta tca c
< 13740

13690 13700 13710 13720 13730




tc atg gtt agt gca gca ctg cat aat tct ctt act gtc atg cca tcc gta aga tgc ttt t
< 13800

13750 13760 13770 13780 13790




ct gtg act ggt gag tac tca acc aag tca ttc tga gaa tag tgt atg cgg cga ccg atg t
< 13860

13810 13820 13830 13840 13850




gc tct tgc ccg gcg tca ata cgg gat aat acc gcg cca cat agc aga act tta aaa gtg c
< 13920

13870 13880 13890 13900 13910




tc atc att gga aaa cgt tct tcg ggg cga aaa ctc tca agg atc tta ccg ctg ttg aga t
< 13980

13930 13940 13950 13960 13970




cc agt tcg atg taa ccc act cgt gca ccc aac tga tct tca gca tct ttt act ttc acc a
< 14040

13990 14000 14010 14020 14030




gc gtt tct ggg tga gca aaa aca gga agg caa aat gcc gca aaa aag gga ata agg gcg a
< 14100

14050 14060 14070 14080 14090




ca cgg aaa tgt tga ata ctc ata ctc ttc ctt ttt caa tat tat tga agc att tat cag g
< 14160

14110 14120 14130 14140 14150




gt tat tgt ctc atg agc gga tac ata ttt gaa tgt att tag aaa aat aaa caa ata ggg g
< 14220

14170 14180 14190 14200 14210




tt ccg cgc aca ttt ccc cga aaa gtg cca cct gac gtc
< 14258

14230 14240 14250

















































































































































































































































































































































































































































































































































































































































































































































































































Features:
T7-g10 Promoter: [1:49]
Hammerhead Ribozyme: [50:107]
VSV Leader: [108:170]
N: [171:1439]
P: [1503:2300]
M: [2360:3049]
Bnv.BG505 immunogen: [3198:5357]
L: [5479:11808]
VSV Trailer: [11809:11907]
Hepatitis Delta Virus Ribozyme: [11913:11991]
T7 Terminators: [11992:12260]
pSP72: [12261:14258]






SEQ ID NO: 2
































It is to be understood and expected that variations in the principles of invention as described above may be made by one skilled in the art and it is intended that such modifications, changes, and substitutions are to be included within the scope of the present invention.
Although the present invention and its advantages have been described in detail, it should be understood that various changes, substitutions and alterations can be made herein without departing from the spirit and scope of the invention as defined in the appended claims.
The present invention will be further illustrated in the following Examples which are given for illustration purposes only and are not intended to limit the invention in any way.
Example 1: VSVΔG-Env.BG505 Vaccine—Live Attenuated VSV-HIV Chimera Delivering Env Trimers
Vesicular stomatitis virus (VSV) has been modified to generate a live chimeric virus vaccine (VSVΔG-Env.BG505) for active immunization against HIV. The replication-competent recombinant chimera delivers a functional HIV Env glycoprotein trimer (clade A.BG505) in the context of viral replication mimicking native HIV spike presentation during an HIV infection.
The VSVΔG-Env.BG505 chimera was constructed by replacing the natural VSV glycoprotein (G) gene with coding sequence for Env.BG505 ( FIG. 1 ). As a result, Env is the only transmembrane glycoprotein encoded by the chimera, and virus propagation and spread is dependent on expression of functional Env trimers and infection of CD4+/CCR5+ cells.
VSVΔG-Env.BG505 is generated from a VSV genomic DNA clone that was developed from a lab-adapted strain of VSV (Indiana serotype). The genomic sequence is similar, but not identical, to the VSV genomic clone developed at Yale University (1), which is used for other VSV-based vaccine candidates including the attenuated VSV-N4CT1 vector developed by Profectus and NIAID (2), and the VSVΔG-Ebola virus chimera developed by the National Microbiology Laboratory in Canada (3), NewLink Genetics, and Merck Vaccines (4-6). About 100 nucleotides out 11 kb differ between the Yale and IAVI genomic clones.
Live VSVΔG-Env.BG505 is recovered from plasmid DNA by electroporating cells with the modified VSV genomic clone ( FIG. 1C ), a plasmid encoding T7 RNA polymerase to synthesize genomic RNA copies, and five plasmids that provide VSV polypeptides (N, P, M, G, L) in trans to initiate virus replication (9). The virus rescue protocol does not require proprietary transfection reagents or helper virus, and it has been optimized for use with Vero cell substrates (protocol adapted from (10, 11)). Recovery of infectious VSVΔG-Env.BG505 can be initiated by electroporating plasmids into Vero cells derived from a qualified cell bank (cells from Meridian Life Science, Inc. are used at IAVI), after which the virus must be propagated in cells that express CD4 and CCR5 to support Env-dependent replication. Thus, recombinant virus amplification, clonal isolation, virus seed preparation, and vaccine production is performed with a modified Vero cell line that contains the genes for human CD4 and CCR5 (VeroCD4/CCR5).
Applicants developed a stable VeroCD4/CCR5 cell line for propagation of the VSVΔG-Env.BG505 chimera. The cell line used in the lab currently encodes human CD4 and CCR5 and was developed under research conditions starting with cells obtained from the Meridian Life Science qualified Vero cell bank. The research VeroCD4/CCR5 cell line is stable and has been used for several years to support work on VSVΔG-Env.BG505 and a number of similar chimeric viruses. Yields of VSVΔG-Env.BG505 produced in VeroCD4/CCR5 monolayers typically are >1×10 7 pfus per ml of harvested culture medium. Work on deriving a new cell line has been initiated for the purpose of generating VeroCD4/CCR5 cells that will meet requirements associated with future VSVΔG-Env.BG505 cGMP manufacturing. As used herein, VERO-CD4/CCR5, VeroCD4/CCR5 and VERT or VERT3 are used interchangeably.
The VSVΔG-Env.BG505 vaccine tested in rhesus macaques contained ‘pseudotyped’ (12) virus particles to enhance vaccine uptake and promote a vigorous initial round of infection and replication. When virus was grown to produce a batch of vaccine, infection was conducted under conditions in which the VSV G glycoprotein was transiently expressed in VeroCD4/CCR5 cells allowing production of particles containing G. An efficient laboratory method was developed to simplify addition of the G pseudotype. A suspension of VeroCD4/CCR5 cells is mixed with plasmid DNA encoding G and VSVΔG-Env.BG505 particles after which the mixture is subjected to electroporation. The electroporated cells are then distributed into cell factories containing culture medium. Virus is harvested and purified 48 hours post-electroporation.
Two points about G pseudotyping and the VSVΔG-Env.BG505 vaccine are worth emphasizing. First, VSVΔG-Env.BG505 does not contain the G gene; thus, infected cells do not express G and the VSV glycoprotein is present only in pseudotyped virus particles used for vaccination. Following vaccination, progeny VSVΔG-Env.BG505 particles produced by the first round of replication will lack the G glycoprotein making all subsequent rounds of infection dependent on HIV Env and infection of CD4+/CCR5+ cells of lymphoid origin. Because G is present only transiently ( FIG. 2 ), it cannot promote spread of infection to other types of cells and tissues (i.e. neurons in the central nervous system).
The second point is related to the benefit of the pseudotyping. It is well established that G is a very effective virus attachment protein, which has been used to pseudotype a variety of different candidate viral vaccines, gene therapy vectors, and oncolytic agents (12-15). A positive effect of pseudotyping on immunogenicity of a prototype VSVΔG-SIV Env chimera was demonstrated experimentally in a small pilot macaque study in which animals were vaccinated mucosally (combination of oral and nasal cavity) with a vaccine prepared with and without a G pseudotype. In animals vaccinated with pseudotyped virus particles, anti-SIV Env antibody titers were greater than 100-fold higher ( FIG. 5 ). Moreover, the transient exposure to G in the virus inoculumn did not elicit significant titers of anti-G antibodies (data not shown).
Many different glycoproteins may be used to pseudotype VSV particles besides G. Alternative pseudotypes may be useful for targeting vaccine delivery to different areas. Examples include F plus H from morbilliviruses, the F and HN from various parainfluenza viruses, the F and G from various pneumoviruses, the F plus HN from various rubulla viruses. Also, the glycorpteins from filoviruses or arena viruses, among others.
Although the efficacious VSVΔG-Env.BG505 vaccine was a pseudotyped particle, it is important to note that studies have not yet been done in macaques to assess whether pseudotyping contributes to vaccine efficacy. Furthermore, G was selected for pseudotyping because it was known to be highly effective, but other alternative viral glycoproteins can be used if it becomes necessary to develop a pseudotyped vaccine that targets a more limited cell population.
The VSVΔG-Env.BG505 vaccine was designed to deliver authentic HIV envelope (Env) trimers mimicking the presentation of Env spikes by HIV infection or a live attenuated HIV vaccine. As designed, the replication competent chimeric virus provides several important immunostimulants once administered, including: 1) innate signaling initiated by infection and replication of an RNA virus; 2) infected cells containing Env incorporated in the cell surface membrane; and 3) progeny virus particles containing Env spikes arrayed on their surface. Moreover, like HIV or SIV, Env-dependent VSVΔG-Env.BG505 propagation in vivo might contribute to vaccine efficacy by providing more persistent antigen exposure and immune stimulation that is associated with infection occurring in lymphoid tissues (16, 17).
VSVΔG-Env.BG505 is designed to propagate using Env as its attachment and entry protein. This has several important consequences during chimeric virus replication in the vaccinee, including: 1) there is strong selective pressure to maintain the gene encoding functional Env; 2) it ensures that the replicating chimeric virus will present the immune system with authentic Env spike targets; and 3) because Env is functional and incorporated in the membrane, it has the conformational flexibility of a native spike and will expose the immune system with a full range of authentic antigenic determinants. Related to the last point, it also is important to emphasize that the functional Env.BG505 trimer expressed by VSVΔG-Env.BG505 is not a conformationally constrained trimer like some other experimental vaccines that have been develop recently like Env.BG505 SOSIP or Env.BG505 NFL described by others (18, 19).
Rose and colleagues first demonstrated that it was feasible to generate an infectious VSVΔG-Env chimera using a clade B Env (23), but additional development was necessary to advance an effective vaccine candidate. First, the Env.BG505 immunogen was selected specifically because it was known to have a broad antigenicity profile (24) and it was isolated from an infected infant that produced bnAbs (25, 26). Second, it was necessary to investigate Env modifications for a number of reasons, including 1) to ensure Env gene genetic stability; 2) to enable vigorous replication in cell culture that would support vaccine production; and 3) to substantially increase Env incorporation into to the infected cell membrane and virus particle to provide improved display of Env spike immunogens. Following an approached suggested by earlier data showing that the Env cytoplasmic tail caused vector genetic instability (unpublished and (27)) and suppressed incorporation into VSV particles (28), a number of hybrid Envs were designed and evaluated ( FIG. 3 ) in which various combinations of the Env signal peptide (SP), transmembrane (TM) region, and cytoplasmic tail (CT) were replaced with sequence from VSV G (Indiana serotype). A hybrid Env containing the VSV G SP, TM and CT was found to be expressed abundantly on the cell surface of transfected cells and also was found to support efficient Env-dependent replication of the VSVΔG-Env.BG505 chimera in CD4+/CCR5+ cells. A hybrid in which the Env membrane-proximal external region (MPER) also was replaced with the analogous ‘Stem’ domain of G was expressed in modestly greater quantities on the surface of transfected cells, but since it lacked the important Env MPER epitope, all subsequent vector design has focused on the Env hybrids where the SP, TM, and CT are substituted with VSV G sequences. Therefore, the VSVΔG-Env.BG505 vaccine encodes a highly expressed Env-G hybrid, which is designed so that all sequence displayed on the membrane surface is Env ectodomain while intracellular and membrane-spanning sequences are derived from G.
The Env-G hybrid immunogen incorporated on the surface of infected cells and VSVΔG-Env.BG505 particles is broadly antigenic. An example of infected cells analyzed by flow cytometry ( FIG. 4B ) shows that multiple mAbs bind the cell surface including PGT145, PGT151 and VRC06, which bind preferentially to determinants formed by well-ordered trimmers (19, 21, 22). Similarly, bnAbs recognize purified virions when they are adsorbed to alum and the alum-virus complexes are analyzed by flow cytometry ( FIG. 4D ), which agrees with electron microscope images ( FIG. 4C ) showing surface density consistent with the present of glycoprotein complexes on the surface of VSVΔG-Env.BG505 particles.
Part of the vaccine design objective was to develop a chimeric virus that could be administered effectively by a mucosal route to stimulate immune protection at the mucosal barrier. Even though a mucosal application of the live vaccine may be advantageous, Applicants do not envision the vaccine to be limited to this route of administration. Because research and development on lentivirus virus vectors has shown that Env is not an effective attachment protein for virus particle delivery, VSVΔG-Env.BG505 modifications were considered that might significantly improve virus uptake without changing the key feature of the chimeric virus, which is its unique design in which Env is the sole glycoprotein expressed following infection. Thus, rather than genetically modifying the VSVΔG-Env.BG505 vector further, a decision was made to test vaccines in which the virus particles were prepared with a G pseudotype, as a considerable body of work on lentiviruses (12) as well as a variety of chimeric VSV vectors (29) showed that pseudotyping with G was effective.
To support testing of a pseudotyped VSVΔG-Env vaccine, a simple system was developed to add G to virus particles. Briefly, a suspension of VeroCD4/CCR5 cells is mixed with plasmid DNA encoding G and VSVΔG-Env.BG505 particles and then mixture is subjected to electroporation. The electroporated cell suspension is then distributed into cell stacks and cultured for ˜48 hours after which pseudotyped virus particles are harvested and purified. The efficiency of pseudotyping can then be quantified by evaluating plaque formation on CD4+/CCR5+ cell monolayers in which Env or G can direct infection, and comparing this to G-mediated infection of standard Vero monolayers, which support a single-cycle of infection that can be quantified by immunostaining to detect individual cells expressing viral proteins.
A pilot study was conducted in Indian rhesus macaques with a prototype VSVΔG-SIV chimera ( FIG. 5A , VSVΔG-SIV-GagEnv). Macaques were used for this early study because transgenic or ‘humanized’ small animal models that can support replication of a CD4/CCR5-tropic virus have limitations. The macaque study was conducted for three primary reasons: 1) assess the ability to safely vaccinate mucosally in the nasal and oral cavity with a chimeric virus; 2) detect and quantify serum anti-Env antibodies elicited by mucosal vaccination; and 3) compare vaccines prepared with and without a G pseudotype.
Macaques were vaccinated ( FIG. 5B ) at weeks 0 and 6 by applying virus solution to the nasal and oral cavities (1×10 8 pfus per site). Importantly, animal behavior was normal following vaccination and no lesions were observed in or around the nose or mouth. Quantification of antibody titers by bioplex assay (30) showed that the chimeric virus vaccines were immunogenic and that the pseudotyped vaccine was significantly more potent. Following the first vaccination, samples analyzed at week 6 showed that the pseudotyped VSVΔG-SIV-GagEnv vaccine elicited low but detectable antibody titers, while animals vaccinated with an ‘empty’ VSV vector or the chimeric virus lacking the G pseudotype had values near baseline. Env antibody titers increased after homologous boost at week 6, and it was clear that the peak titer elicited by the pseudotyped chimera was considerably stronger (>1,000×) compared to the magnitude of the response generated by the vaccine lacking the G pseudotype, and the titers also remained substantial >2.5 months after the week-6 boost. It also is worth highlighting that two mucosal vaccinations with the pseudotyped VSVΔG-SIV-GagEnv vaccine generated antibody titers that were in the same range as peak responses seen with a relatively potent vaccination regimen based on 3×DNA-SIV-Env prime (intramuscular electroporation) and Ad5-SIV Env (intramuscular) boost (31).
Several conclusions were drawn from this pilot study. First, the chimeric virus vaccine was able to safely elicit anti-Env antibodies against a membrane anchored Env spike. Second, antibody titers of this magnitude elicited by mucosal vaccination indicated that the VSVΔG-SIV chimera replicated following vaccination and that the antibody response was not elicited simply by exposure to the virus particles delivered in a buffered solution. This assumption also is consistent with the fact that G in the pseudotyped particles did not elicit an anti-G response significantly above background in an ELISA (data not shown). Finally, it was evident that the chimeric virus vaccine prepared with the G pseudotype was more immunogenic, thus the HIV vaccine based on VSVΔG-Env.BG505 was advanced for testing in macaques as a pseudotyped vaccine.
The preclinical efficacy of the VSVΔG-Env.BG505 vaccine prepared with a G pseudotype is being evaluated in Indian rhesus macaques using the rectal SHIV challenge model. The study was designed with the three main objectives: 1) show that the VSVΔG-Env.BG505 chimera could be administered safely to the nasal and oral cavities; 2) demonstrate that vaccination elicits anti-Env antibodies; and 3) establish that vaccination provides measurable protection from rectal exposure with a heterologous clade B SHIV (SHIV SF162p3).
The study also included a head-to-head comparison with a second VSV vector encoding the same Env.BG505 trimer immunogen. The main purpose of this comparison was to evaluate an alternative Env.BG505 delivery vector (VSV-G6-Env.BG505, FIG. 6 ) that would have increased replicative capacity in vivo. To achieve greater replicative capacity, the VSV-G6-Env.BG505 vector was designed to contain genes encoding Env.BG505 and G; therefore, the vector coexpresses the glycoproteins in infected cells, and incorporate both trimeric complexes in virus particles. As designed, the VSV-G6-Env.BG505 vector can propagate and spread in a wider range of cells in vivo because the continuous expression of G allows infection and spread into a much broader range of cell types. Thus, both the pseudotyped VSVΔG-Env.BG505 chimera and VSV-G6-Env.BG505 can infect most cell types at the site of vaccine administration using G, but after the initial round of replication, secondary infection initiated by progeny virus particles will be significantly different, with the VSVΔG-Env.BG505 targeted specifically to CD4+/CCR5+ cells and VSV-G6-Env.BG505 being able to spread into multiple cell types.
The preclinical efficacy study was designed with three groups of 10 macaques (negative for Mamu-B*08 and -B*17 MHC alleles associated with immune control) that were vaccinated at weeks 0, 4, and 29 with pseudotyped VSVΔG-Env.BG505, VSV-G6-Env.BG505 or a saline control. It is important to highlight that vaccination was conducted only with the live VSV vectors, and no boost was performed with a heterologous vaccine. Vaccines were administered by application to mucosal surfaces in the nasal and oral cavity of sedated animals (1×10 8 pfus per site). No local lesions were observed and all macaques behaved normally after vaccination.
All macaques immunized with a VSV-based Env.BG505 vaccine developed detectable anti-Env serum antibodies after the second vaccination. The third vaccination at week 29 provided a boost, and perhaps more importantly, increased the durability of the antibody titiers, which persisted during the 5-month rest period before challenge in 8 out of 10 macaques vaccinated with VSVΔG-Env.BG505 and all animals vaccinated with VSV-G6-Env.BG505. The TZM-bl assay (33) also was used to analyse serum for virus-neutralizing antibodies (nAbs). The resulted showed that nAb titers were low (titers ≦100) and were detectable in only some vaccinated animals (summarized on the ELISA chart in FIG. 8 ). In macaques vaccinated with the VSVΔG-Env.BG505 chimera, 4 animals were positive for nAbs active against HIV SF162p3 pseudovirus at week 31, but the titers waned to undetectable by the day of SHIV challenge. Vaccination with VSV-G6-Env.BG505 elicited nAbs against SF162p3 and homologous BG505 pseudovirus that were detectable at week 31 and 48, but not in all animals.
Clade B SHIV SF162p3 challenge commenced at week 48, which was about 5 months after the final vaccination ( FIG. 7 ). The challenge protocol was composed of 3 stages: the first 5 rectal exposures conducted approximately every two weeks, a 6-week rest period, and the final 5 biweekly exposures. Macaques with ≧200 genome SHIV copies per ml of plasma were considered infected after which challenge was stopped. All infected macaques were viremic for weeks following the initial infection ( FIG. 9 ) as determined by detection of SHIV genomes in the blood, and accordingly, the infected animals developed antibodies against Gag expressed by the SHIV (data not shown).
The SHIV infection rate was significantly reduced in macaques vaccinated with the VSVΔG-Env.BG505 chimera compared to animals vaccinated with VSV-G6-Env.BG505 or saline control ( FIG. 10 ). Over the course of 9 challenges, 9 out of 10 macaques in the Control and VSV-G6-Env.BG505 groups became chronically infected with SHIV at a similar frequency. In contrast, in macaques vaccinated with VSVΔG-Env.BG505, just 3 were infected with challenge virus indicating that VSΔG-Env.BG505 immunization significantly increased resistance to mucosal SHIV infection. Thus, vaccine efficacy as measured by prevention of rectal infection with a heterologous clade B SHIV was 67%.
Immunologic assessment continues, but current results point to a potential relationship between the reduced frequency of infection seen in the animals vaccinated with the VSVΔG-Env.BG505 vaccine ( FIG. 10 ) and Env-specific serum antibodies. First, both replication-competent VSV vectors elicited serum antibodies that persisted for the 5-month period between the final vaccination and the beginning of the repetitive SHIV challenge protocol ( FIG. 8 ). In the animals vaccinated with VSVΔG-Env.BG505, there were 2 animals in which the antibody titers waned to baseline levels by week 48 when challenge commenced ( FIG. 8 ), and interestingly, these were the same two animals that appeared least resistant in this group and became infected by challenge 2 ( FIG. 10 ). The third animal that became infected in this group resisted 7 challenges conducted over a period of about 4.5 months, but became infected at exposure 8 by which time the serum antibody titers had waned. These results imply that there is a relationship between Env.BG505 gp120 binding antibody titers and SHIV infection resistance. This trend is summarized graphically in FIG. 11 .
In contrast to the results seen in animals vaccinated with the VSVΔG-Env.BG505 chimera, that rate of infection in macaques vaccinated with VSV-G6-Env.BG505 was very similar to the control group indicating that vaccination did not have measurable effect on SHIV infection frequency ( FIG. 10 ). This was observed even though all animals had developed Env antibodies in response to vaccination, including some macaques that had nAbs ( FIG. 8 ).
Taken together, the results of vaccination with the different live VSV-based vectors show that both types of vaccine elicit Env antibodies, but that the quality of the antiviral immunity is very different. What is responsible for this difference in protection is not understood at this time, but perhaps it is related to antibody binding site specificity, the diversity of Env epitopes recognized, or IgG effector functions. Alternatively, the two live vectors might elicit different profiles of Env-specific T cells with antiviral activity that is affecting infection resistance. Ongoing and future immunologic assessment will help identify differences in the immune responses elicited by the two vaccines, which will provide guidance for vector and immunogen improvements.
The results produced with two different replicating VSV-based vaccines also illustrates clearly that specific vaccine design details can have a pronounced effect on efficacy. Some of the unique features of the VSVΔG-Env.BG505 vaccine that might contribute to efficacy, include; 1) CD4+/CCR5+ tropism that targets replication to lymphoid cells and tissues; 2) chimeric virus propagation in vivo that is dependent on expression of functional Env and will provide immune system exposure to authentic Env spikes; 3) the only glycoprotein expressed is Env, thus there is no other competing glycoprotein immunogen that might dominate immune responses; and 4) the lack of other vector-encoded glycoproteins eliminates development of potent anti-vector antibodies that might interfere with multiple immunizations.
Preclinical efficacy in the SHIV challenge model was observed following mucosal vaccination with a total dose of 2×10 8 pfu per ml. The vaccine dose was split between two sites. Mucosal surfaces in the nasal and oral cavities each received 1×10 8 pfu applied in a buffered solution.
Preclinical efficacy in the SHIV challenge model was observed with a vaccination schedule of 0, 4, and 29 weeks. Other vaccination schedules are also contemplated.
Mucosal vaccination in the nasal and oral cavity was tested primarily because the goal was to stimulate enhanced mucosal immunity. Other considerations supporting this vaccination route included: 1) providing access to submucosal CD4+/CCR5+ lymphocytes that would be targets for VSVΔG-Env.BG505 replication, and 2) VSV naturally infects these mucosal sites.
VSVΔG-Env.BG505 is a recombinant chimeric virus based on the VSV Indiana serotype. The VSV G gene deleted and replaced with sequence encoding functional HIV Env.BG505. The live vaccine is replication competent and propagates specifically in cells that contain the CD4/CCR5 receptors.
The efficacious preclinical vaccine is a G-pseudotyped VSVΔG-Env.BG505 that is applied to nasal and oral cavity mucosal surfaces at 0, 4, and 29 weeks.
The VSVΔG-Env.BG505 vaccine is expected to be safe for use in humans, because 1) no observable adverse reactions occurred in vaccinated macaques, and 2) the chimeric virus design makes propagation dependent on Env, thus virus spread in vivo is restricted to lymphoid cell and tissues that express CD4 and CCR5 and will prevent virus replication in other sites like the central nervous system.
The preferred cell line for vaccine production is VeroCD4/CCR5, which has been used to support preclinical development of the VSVΔG-Env.BG505 chimeric virus vaccine. A similar cell line must be ‘rederived’ using conditions and materials that are consistent with using the cells for vaccine manufacturing. Manufacturing processes and steps are set forth in FIG. 12 . Preparation of VSVΔG-Env.BG505 with G pseudotype is set forth in FIG. 13 .
Preclinical material tested in macaques may be purified by 2 round of centrifugation through sucrose cushion and the method is based on tangential flow filtration.
Preclinical vaccine material is stored frozen (−80) in Hank's Balanced Salt Solution (HBSS) supplemented with 15% trehalose.
Raw material and biological starting material suitability, quality, and characterization (e.g., passage history of cell substrate and viral seed material) may include:
Recombinant VSVΔG-Env.BG505 is generated from a plasmid DNA containing a modified VSV genomic clone in which the G gene is replaced with sequence encoding HIV Env.BG505. Rescue of recombinant virus is initiated by electroporating the genomic clone with supporting plasmids that direct expression of VSV N, P, M, G, and L proteins and T7 phage RNA polymerase. The VSV genomic clone is based on the VSV Indiana serotype. The VeroCD4/CCR5 cell line used for preclinical development was generated starting with Vero cells from a cell bank qualified cell bank (obtained from Meridian Life Science, Inc). The VeroCD4/CCR5 cell line was generated by microporating cells with a plasmid that contains genes for expression of human CD4 and CCR5 and the Neo resistance marker. VeroCD4/CCR5 is typically propagated in monolayer cultures. Cell factories are used for virus production. The cells are grown in DMEM supplemented with 10% fetal bovine serum from certified suppliers. Virus amplification can be conducted in monolayers in which the medium is exchanged with serum-free growth medium such as VPSFM.

Preclinical vaccine characterization may include:
Potency: Virus is quantified by plaque assay on VeroCD4/CCR5 cells. To confirm virus particles are pseudotyped with G, standard Vero monolayers are infected and the single-cycle infection in incubated overnight. Monolayers are subsequently immunostained to quantify infected cells.

Additional vaccine virus characterization:
Genome copies (qPCR) per infectious unit Genomic nucleotide sequence Env insert integrity by PCR Env expression by Western blot Env expression detected on infected cells by flow cytometry and bnAbs Virus purity by denaturing gel electrophoresis and silver stain Mycoplasma testing by PCR Endotoxin testing

Assay development required to support lot release or product characterization may include:
Potency—see above, plaque assay and genome-to-pfu ratio Safety:
Env insert integrity by PCR Lack of VSV G gene by PCR Genomic sequence Infection of Vero cells with pseudotyped virus and subsequent blind passage to confirm lack of CPE indicating that virus is CD4/CCR5-dependent as expected


Preparation of reagents to develop assays may include:
Primers and probes are available to assess genomic sequences, quantify genome copies, and specifically detect the Env gene insert. Antibodies that can neutralize the pseudotyped VSVΔG-Env.BG505 chimera are required for adventitious agent testing. Antibodies recognizing the G pseudotype block infection in eggs, mice, and most cell lines provided they do not express primate CD4/CCR5.

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Barouch D H, Alter G, Broge T, Linde C, Ackerman M E, Brown E P, Borducchi E N, Smith K M, Nkolola J P, Liu J, Shields J, Parenteau L, Whitney J B, Abbink P, Ng'ang'a D M, Seaman M S, Lavine C L, Perry J R, Li W, Colantonio A D, Lewis M G, Chen B, Wenschuh H, Reimer U, Piatak M, Lifson J D, Handley S A, Virgin H W, Koutsoukos M, Lorin C, Voss G, Weijtens M, Pau M G, Schuitemaker H. HIV-1 vaccines. Protective efficacy of adenovirus/protein vaccines against SIV challenges in rhesus monkeys. Science. 2015; 349(6245):320-4. doi: 10.1126/science.aab3886. PubMed PMID: 26138104. 33. Sarzotti-Kelsoe M, Bailer R T, Turk E, Lin C L, Bilska M, Greene K M, Gao H, Todd C A, Ozaki D A, Seaman M S, Mascola J R, Montefiori D C. Optimization and validation of the TZM-bl assay for standardized assessments of neutralizing antibodies against HIV-1. J Immunol Methods. 2014; 409:131-46. doi: 10.1016/j.jim.2013.11.022. PubMed PMID: 24291345; PubMed Central PMCID: PMCPMC4040342.

Example 2: Vaccination with a Live Vesicular Stomatitis Virus-HIV Env Chimera Prevents SHIV Infection
Seven of 10 Indian rhesus macaques vaccinated with a novel replication-competent vesicular stomatitis virus vector designed with functional HIV Env substituting for the native VSV glycoprotein remained uninfected after repeated rectal challenge with a heterologous clade B SHIV.
HIV is a challenging vaccine target because its functional envelope glycoproteins (Envs) are highly glycosylated, sequence diverse, and assembled into a compact trimeric complex (the Env spike) that restricts epitope access. Moreover, vaccines based on non-native forms of Env are either ineffective or provide limited protection. Therefore, Applicants developed a novel spike delivery vaccine (VSVΔG-Env.BG505) from vesicular stomatitis virus (VSV) by replacing the VSV glycoprotein (G) with functional clade A HIV Env. Rhesus macaques vaccinated with live VSVΔG-Env.BG505 developed Env antibodies, and importantly, 7 of 10 remained uninfected after repeated rectal challenge with heterologous clade B SHIV SF162p3. In contrast, a second more typical VSV vector expressing both Env and G induced Env antibodies but failed to protect, showing that the VSVΔG-Env.BG505 vector design was associated with preclinical efficacy. Applicants' results indicate that the VSVΔG chimeric virus platform is an important developing vaccine technology for HIV Env glycoprotein delivery.
HIV is a challenging vaccine target because its functional envelope glycoproteins (Envs) are highly glycosylated, sequence diverse, and assembled into a compact trimeric complex (the Env spike) that restricts epitope access. Moreover, vaccines based on non-native forms of Env are either ineffective or provide limited protection. Therefore, Applicants developed a novel spike delivery vaccine (VSVΔG-Env.BG505) from vesicular stomatitis virus (VSV) by replacing the VSV glycoprotein (G) with functional clade A HIV Env. Rhesus macaques vaccinated with live VSVΔG-Env.BG505 developed Env antibodies, and importantly, 7 of 10 remained uninfected after repeated rectal challenge with heterologous clade B SHIV SF162p3. In contrast, a second more typical VSV vector expressing both Env and G induced Env antibodies but failed to protect, showing that the VSVΔG-Env.BG505 vector design was associated with preclinical efficacy. Applicants' results indicate that the VSVΔG chimeric virus platform is an important developing vaccine technology for HIV Env glycoprotein delivery.
Replication-Competent VSV-HIV Env Vaccine Vectors.
The VSVΔG-Env.BG505 chimera was developed by replacing the VSV G gene with sequence encoding functional Env.BG505 ( FIGS. 19A-B with more detail in the Materials and Methods). In addition to expressing Env and replicating with the cell tropism of HIV, the VSVΔG-Env.BG505 chimera has several other features to highlight. First, its dependence on Env.BG505 for propagation ensures that some functionally-configured Env is expressed during viral replication that will expose the immune system to authentic Env spikes. Second, because the vector lacks the G gene, negative effects caused by G expression are avoided, such as the VSV glycoprotein dominating B cell responses or inducing potent anti-vector immunity. Finally, cells infected with VSVΔG-Env.BG505 produce progeny virus particles containing Env arrayed on their surface, which is expected to substantially enhance immunogen presentation to B lymphocytes (11).
To directly investigate whether the live VSVΔG-Env.BG505 chimera was advantageous for the reasons mentioned above, VSV-G6-Env.BG505 ( FIG. 19C ) was developed as a comparator for use in the macaque study described below. VSV-G6-Env.BG505 is a more typical VSV vector in which the Env.BG505 gene was added as an extra transcription while retaining G. The vector was generated by reintroducing the G gene at the terminus of the negative-sense RNA genome ( FIGS. 19A and C; G in genome position 6), which maintained Env in the same genomic position relative to the promoter ( FIG. 19A ) as in VSVΔG-Env.BG505 and modestly downregulated G expression (16). VSV-G6-Env.BG505 propagates efficiently using G, which recognizes a ubiquitous cellular receptor that enables infection of a broad range of cell types (17); thus, including VSV-G6-Env.BG505 in the vaccine study allowed us to ask whether this G-dependent vector might deliver the Env spike more effectively, perhaps because constitutive G expression confers increased replicative capacity in vivo, a different cell and tissue tropism, or both.
Env.BG505 expression by the two different VSV vectors was compared by infecting cultured cells and conducting flow cytometry using monoclonal antibodies that bind a variety of Env epitopes (4-6). When VERO cells or a stable VERO derivative (VERO-CD4/CCR5) expressing human CD4 and CCR5 were exposed to VSVΔG-Env.BG505, only the CD4+/CCR5+ cells were infected as shown by Env detected on the cell surface ( FIG. 19D ). The expanded tropism conferred by G allowed VSV-G6-Env.BG505 to infect both cell types although the intensity of Env surface staining was reduced compared to VERO-CD4/CCR5 cells infected with VSVΔG-Env.BG505. The more intense cell surface staining produced by VSVΔG-Env.BG505 infection was due at least in part to increased Env expression, which was detectable by Western blot analysis (data not shown), but it also was possible that G co-expression by cells infected with VSV-G6-Env.BG505 had a negative effect on Env incorporation into the cell plasma membrane. It also is important to note that the panel of monoclonal antibodies used for flow cytometry included some that recognize native Env spikes structures (PGT145, PGT151, and VRC06b) as well as others (IgGb6 and F105) that bind epitopes that are exposed when the Env subunits are not assembled into a compact spike (18-20). Infected cells were bound by all antibodies included in the panel demonstrating that multiple forms of Env were expressed on the cell surface including well-ordered Env spikes, as is typical for an HIV infection (21).
Because Env spikes arrayed on progeny virions produced during replication in vivo were expected to be important immunogens (11), the antigenicity of purified virus particles was analyzed with a modified flow cytometry assay. In this assay, virus particles are adsorbed to aluminum phosphate (alum) to generate alum-virus complexes that can be incubated with monoclonal antibodies and are large enough to be analyzed with a flow cytometer (16). Subsequent analysis with the same monoclonal antibody panel showed that substantially more Env was incorporated in the VSVΔG-Env.BG505 chimera compared to VSV-G6-Env.BG505 ( FIG. 19E and note different Y axes), which also was confirmed by Western blotting (data not shown). The flow cytometry data also showed that the antigenicity of VSVΔG-Env.BG505 virions was similar to the infected cell surface ( FIG. 19D ), including binding by VRC06b, PGT145 and PGT151. In summary, analysis of purified virions showed that both VSVΔG-Env.BG505 and VSV-G6-Env.BG505 contained Env, but the immunogen was considerably more abundant in the VSVΔG chimeric virus particle.
Vaccination and Preclinical Efficacy.
Three groups of 10 male Indian rhesus macaques were vaccinated by administering live vector or saline control to both intranasal and intraoral surfaces at 0, 4 and 29 weeks ( FIG. 20A ). The five-month break between the second and third vaccination was included to provide time for germinal center reactions and B cell differentiation (22). All immunizations were conducted with a VSV vector, and no booster vaccinations were administered with a heterologous vector or subunit vaccine.
No adverse reactions were observed after vaccination. Virus shedding into the oral cavity was analyzed using qRT-PCR, which showed that viral genomes were low to undetectable for VSVΔG-Env.BG505 but increased for VSV-G6-Env.BG505 particularly following the first vaccination ( FIG. 25 ). This result implied that the replicative capacity of VSV-G6-Env.BG505 was greater, but it might also be due to differences in cell and tissue tropism affecting shedding into the oral cavity. VSV genomes were not detected in the blood (data not shown) in either group, which was consistent with lack of viremia detected in earlier studies (23). Interestingly, VSVΔG-ZEBOV did cause transient viremia in macaques (13) and clinical trial participants (14, 15), which might reflect an effect of cell tropism conferred by the Ebola virus glycoprotein.
Intrarectal SHIV SF162p3 challenge commenced at week 48, about 4.5 months after the third vaccination ( FIG. 20A ). This rest period prior to SHIV challenge allowed waning of peak adaptive immune responses as well as decay of innate immunity that might have been triggered by VSV. A maximum of 10 sequential challenges were planned ( FIG. 20A ), with the first five being conducted approximately every 2 weeks after which a brief rest period was included to allow innate immune responses to decline if any were induced by repeated SHIV exposure (24, 25). Challenged animals that had 200 SHIV genome copies or more on two successive blood draws were considered positive ( FIG. 26 ), at which time challenge was stopped. All vaccinated animals that tested positive for SHIV genomes also developed antibodies against Gag expressed by the SHIV ( FIG. 27 ).
After completing repetitive SHIV challenge, 9 of 10 placebo control animals were infected but just 3 of 10 in the VSVΔG-Env.BG505 group ( FIG. 20B ). This indicated that the VSVΔG-Env.BG505 group was significantly protected with an overall efficacy of 67% (P=0.014). The per-challenge vaccine efficacy for VSVΔG-Env.BG505 was estimated to be 79.8% based on a Leaky vaccine model (26). In contrast, vaccination with VSV-G6-Env.BG505 had no protective effect ( FIG. 20B , and Table 1).
Antibody titers in animals 11 and 15 were at the lower measureable limit when SHIV challenge was initiated at week 48 ( FIGS. 20A and B), and both macaques were infected right away at challenge 1 and 2, respectively ( FIG. 20B with more detail in FIG. 29 ). Animal 16 resisted 7 challenges conducted over a period of ˜5 months ( FIGS. 20B and 29 ). By challenge 8 (week 67) when infection occurred in animal 16, titers had declined to near baseline ( FIG. 29B ). Thus, in the three unprotected macaques in the VSVΔG-Env.BG505 group, low binding antibody titers were associated with the timing of SHIV infection.
To determine what regions of Env might be targeted in response to VSVΔG-Env.BG505 vaccination, additional mapping of serum antibody binding specificity was performed with several assays. For conducting ELISAs and Western blots, seven different regions of Env.BG505 ( FIG. 22A ) were expressed as fusion proteins using human serum albumin (HSA) as the N-terminal fusion partner. Fusion to HSA enabled expression of the Env.BG505 fragments as secreted glycoproteins (31). For the ELISA results shown in FIG. 22B , the purified recombinant proteins were captured on microtiter plates (capture ELISA) using their C-terminal His tag after which they were reacted with sera from week 48. Four conclusions can be drawn from the capture ELISA data. First, the predominant positive signal in both vaccine groups was against the HSA-V3C3 and HSA-gp41 (gp41 ectodomain only). These fusion proteins also generated the most frequent and intense signals when used in a Western blot assay ( FIG. 32 ). Second, sera from the three unprotected macaques in the VSVΔG-Env.BG505 group (11, 15, and 16) had lower HSA-V3C3 and HSA-gp41 values consistent with these animals being low responders, as observed earlier with Western blots ( FIGS. 21A-B ). Finally, the HSA-gp41 substrate allowed unambiguous detection of antibodies specific for gp41 in vaccinated animals ( FIGS. 22B and 32 ), which were not observed in the earlier Western blot assays ( FIGS. 21A and 30 ). Lack of gp41 signals in the prior Western blots likely was due to lower gp41 quantities being present on the blot membrane, but perhaps conformation assumed by the different gp41 substrates played some role.
Seven of 10 macaques vaccinated with the live Env-dependent VSVΔG-Env.BG505 chimera remained uninfected after repeated rectal challenge with heterologous clade B SHIV SF162p3 ( FIG. 20 ). Notably, this level of efficacy was produced with a three-dose regimen of VSVΔG-Env.BG505, which differentiates this vaccine from some others evaluated before where protection was observed after immunization with multiple types of vaccine used either in combination or in a heterologous prime-boost regimen (8, 33, 34).
In the 7 protected macaques vaccinated with VSVΔG-Env.BG505, resistance to SHIV infection was associated with persistent Env-specific serum antibodies, while in the three animals that became infected, poor vaccine take or waning antibody titers were a marker of susceptibility ( FIGS. 21, 22 and 29 ). Perhaps the most visual evidence for this was the gp120 ELISA data ( FIG. 29 ) and Western blot results ( FIG. 21 ), which clearly showed that the unprotected animals had reduced quantities of Env-specific serum antibodies. Further analysis of the sera from this group identified statistically significant correlations between the magnitude of antibody binding activity and SHIV infection resistance (6D), but it remains to be determined if the more abundant Env antibodies are directly involved in the protective mechanism or whether they primarily are indicators of VSVΔG-Env.BG505 vaccine take. The suggestion that they contribute to the mechanism of protection might gain support from the data showing that gp120 V3 and gp41 ( FIG. 22 ) were prominent targets of the antibody response induced by VSVΔG-Env.BG505. Antibody binding to V3 and gp41 has been linked to protection before, for example, reduced infection risk was correlated with anti-V3 antibodies in the RV144 clinical trial (32) and anti-gp41 antibodies have been associated with protection from progressive SIV infection in the macaque model(35).
Functional activities associated with the protective antibodies remain to be identified. Even if undetectable quantities of neutralizing serum antibodies were present, their activity likely would not be adequate to mediate protection (36). Maybe mucosal vaccination with VSVΔG-Env.BG505 resulted in neutralizing antibody being tissue associated or in mucosal secretions rather than in circulation, although anti-gp120 antibodies were not detected in oral or rectal swab samples (data not shown). It seems more likely that protection was due to Env-specific immunoglobulins that direct antibody-mediated effector functions, like those induced by other Env vaccine candidates evaluated in recent preclinical studies (33, 34) or the RV144 clinical trial (8). There is growing recognition that antibodies lacking classic in vitro virus neutralizing activity contribute substantially to protection from viral infections, as illustrated by some recent studies on influenza virus (37, 38); thus, further investigation and comparison of effector functions associated with IgG induced by protective VSVΔG-Env.BG505 or nonprotective VSV-G6-Env.BG505 will be informative.
The Western blot results indicated that binding activity persisted for at least a year in protected animals ( FIG. 21D ). This might resemble what is observed during vaccination with live attenuated viruses like in the measles vaccine. Antibody titers established by measles vaccination are considerably lower than those reached during natural infection, but the attenuated virus replicates sufficiently to establish durable protective antibodies (39). There likely is a similar requirement for VSVΔG-Env.BG505 to achieve replication threshold that provides an adequate quantity and duration of Env expression, results in release of immunogenic virus particles containing Env arrayed on their surface (11), and distributes immunogen to lymphoid tissues (40). Possibly, vaccine failure in the three unprotected macaques in the VSVΔG-Env.BG505 group was caused by inadequate replication, thus future studies that investigate VSVΔG-Env.BG505 propagation in vivo will be important.
Replicative capacity might also contribute to a notable difference between the VSVΔG-ZEBOV and VSVΔG-Env.BG505 chimeric virus vaccines. In preclinical and clinical studies (13-15), a single vaccination with VSVΔG-ZEBOV was sufficient for efficacy. A single vaccination with VSVΔG-ZEBOV may be sufficient because the virus apparently replicates and disseminates more extensively based on finding virus in the blood of macaques and clinical trial volunteers (13-15). This suggests that further development of the VSVΔG-Env.BG505 vaccine may benefit from investigating how to safely increase virus replication. This might be achieved by launching a more robust initial infection using a different vaccination route or higher dose, or alternatively, maybe a VSVΔG-Env.BG505 vector can be developed that has increased replicative capacity. A follow up study in macaques is being initiated to investigate some of these variables.
The VSVΔG chimeric virus design appears to be emerging as an important vaccine technology for delivery of viral glycoprotein immunogens. The VSVΔG-ZEBOV clinical trials showed that the Ebola virus vaccine was safe and efficacious (13-15). Promising preclinical results also have been produced with other hemorrhagic fever virus glycoproteins (41), and now Applicants' data shows that this strategy can be adapted for use with an HIV Env trimer immunogen, which is well known to be a very difficult vaccine target (5). The effectiveness of the VSVΔG chimera design probably is due to its ability to reproduce features of a natural pathogen infection without pathology that inhibits development of protective adaptive immunity. Vaccine features such as expression of the native transmembrane glycoprotein on the surface of infected cells, infection directed to cells and tissues specified by the tropism of the foreign glycoprotein, and the presentation of immunogen arrayed on virus particles all likely play important roles in shaping the immune response. Moreover, the lack of a G gene in the vector is very important, because it eliminates expression of a dominant off-target B cell immunogen, prevents development of potent anti-G antibodies, and allows the foreign glycoprotein to be repetitively arrayed on the virus particle without interference from G.
To evaluate whether the promising preclinical performance of VSVΔG-Env.BG505 can be extended to humans, as it was for the VSVΔG-ZEBOV vaccine, Applicants are developing a clinical trial candidate. It is relevant to clinical development to mention that the G gene deletion in VSVΔG-ZEBOV resulted in loss of the VSV neurovirulence phenotype that is observed in some preclinical models (42). Advancing VSVΔG-Env.BG505 to clinical trial will be valuable, as it will answer whether the live chimeric virus platform can be used to safely induce Env binding antibodies with properties like those described above in healthy clinical trial volunteers.
Molecular Cloning, Recombinant Proteins, and Cell Line Development.
The VSV genomic clone is based on the VSV Indiana (IND) serotype (16). The plasmid vector containing the VSV genomic clone was similar to one used before (46) except that the T7 RNA polymerase promoter was replaced with a longer version that improves T7 RNA polymerase processivity (T7-g10 (47) and a hammerhead ribozyme sequence was positioned between the T7-g10 promoter and the beginning of the VSV nucleotide sequence (48). The hepatitis delta virus ribozyme and T7 terminator sequences downstream of the 3′ end of the VSV antigenome were the same as used before (46). Modified genomic clones with the G IND or G New Jersey (NJ) gene moved to genomic position 6 (VSV-G6, FIG. 19C ) were described earlier (16) and a third clone was developed for this study using Maraba (MAR) virus G (Genbank HQ660076.1). Plasmids that express the VSV structural proteins (N, P, M, G, and L) under control of the CMV promoter were used to support VSV rescue (16) instead of those controlled by the T7 promoter used in the earlier procedure (46). A plasmid designed to express T7 RNA polymerase from the CMV promoter was designed similarly to the one described previously (46).
The Env immunogen expressed by VSVΔG-Env.BG505 and VSV-G6-Env.BG505 was based on the wild-type clade A Env.BG505 amino acid sequence (Genbank ABA61516, 49, 50). Env.BG505 was modified by replacing the signal sequence, transmembrane region and cytoplasmic tail with corresponding regions of G from VSV IND ( FIG. 23A ). The nucleotide sequence encoding the modified Env.BG505 was optimized with a VSV codon bias as described previously (16) after which the gene was inserted in the VSV genomic clone in place of G. Additional VSVΔG-Env chimeras were developed similarly based on Env C.CH505 (week 100; Genbank KC247391.1) and Env B. SF162p3 (Genbank KF042063).
A series of plasmids also were constructed to allow expression of several different domains of Env.BG505 fused to the C-terminus of human serum (HSA, 31). A glycine-serine linker (GGGGS(SEQ ID NO: 3)) was inserted between the C-terminus of HSA and the Env sequence, and a C-terminal histidine tag was added to enable chromatographic purification of HSA-fusion proteins secreted from transfected cells. The HSA fusion proteins were expressed by transfecting 293T cells and purified as described previously (49). His-tagged Env.BG505 gp120 (49) and gp140 containing a flexible linker in place of the furin cleavage site (51) were expressed and purified similarly.
A stable VERO cell line expressing human CD4 and CCR5 (VERO-CD4/CCR5) was developed for propagating the VSVΔG-Env.BG505 vector. The human CD4 and CCR5 coding sequences were joined by a 2A-like element (52) to form a single cistron (CCR5-2A-CD4), which was inserted into a plasmid under the control of a transcription unit developed from the human heat shock protein 60 gene (53). A stable cell line was generated by introducing DNA into cells by microporation (Neon Transfection System, Invitrogen) and selecting clonal isolates resistant to G418.
Cell Culture and Virus.
Recombinant virus recovery from DNA and virus propagation was performed using VERO or VERO-CD4/CCR5 cells. Three media were used for VERO cell propagation and electroporation procedures that were similar to those described before (46). VERO cell medium 1 (VCM1) is Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% heat-inactivated fetal bovine serum, 220 μM 2-mercaptoethanol, 2 mM L-glutamine, 1 mM sodium pyruvate, and 0.1 mM MEM nonessential amino acids. VCM2 is Iscove's modified Dulbecco's medium (IMDM) supplemented with 220 μM 2-mercaptoethanol, 1% DMSO, 2 mM L-glutamine, 1 mM sodium pyruvate, and 0.1 mM MEM nonessential amino acids. VCM3 is the same as VCM1 with addition of 50 μg/mL Gentamicin. The VERO-CD4/CCR5 cell line was propagated in VCM3 containing 1 mg per mL G418. All medium and supplements were obtained from ThermoFisher.
Recombinant VSV was rescued from DNA using a helper-virus-free method adapted from Witko et al. (46) using the modified plasmids described above. Virus rescue was initiated by electroporation of plasmids encoding T7 RNA polymerase, VSV N, P, M, G, and L, and the appropriate VSV genomic clone into VERO (for VSV-G6) or VERO-CD4-CCR5 (for VSVΔG) cells. Conditions for electroporation with a BTX ECM 830 instrument (Harvard Apparatus) and subsequent virus recovery were similar to those used in the earlier method (46).
To ensure efficient vaccination with either vaccine, two vector-specific modifications were applied, but the fundamental vaccine designs shown in FIGS. 19A-C were not changed. These modifications enhanced vaccine delivery without altering the Env-dependent propagation of VSVΔG-Env.BG505 or the G-dependent propagation of VSV-G6-Env.BG505. The modifications are illustrated in FIGS. 23 and 24 ). To enhance mucosal VSVΔG-Env.BG505 uptake, vaccine material was prepared as a pseudotyped virus particle bearing G (G pseudotype; FIGS. 23B and 24A -B). This was done simply by amplifying vaccine material in VERO-CD4/CCR5 cells that transiently expressed VSV G. Pseudotyped VSVΔG-Env.BG505 launches a more robust initial infection, because G recognizes a ubiquitous receptor found on a wide range of cells (17). Importantly, G is not expressed by cells infected with pseudotyped VSVΔG-Env.BG505 and all subsequent rounds of infection in vivo are Env dependent ( FIG. 23 ). For VSV-G6-Env.BG505, it was modified to reduce the negative effects of anti-G antibodies that develop during repeated vaccination with vectors expressing G. Three versions of VSV-G6-Env.BG505 ( FIGS. 24A and C) were used in sequence during the three-dose regimen ( FIG. 24A ). Each version of VSV-G6-Env.BG505 differed only in the G gene ( FIG. 24C ), which was exchanged with sequences from three different vesiculoviruses including VSV IND, VSV NJ, and Maraba virus (16, 54).
Large batches of VSVΔG-Env.BG505 or VSV-G6-Env.BG505 were amplified using VERO-CD4/CCR5 or VERO cells, respectively. Cell monolayers were grown in Cell Factories (Corning) using VCM3, but once infection was initiated, the medium was changed to Virus Production Serum-Free Medium (VPSFM, supplemented with 4 mM L-Glutamine, 50 U/mL Penicillin and 50 μg/mL Streptomycin; ThermoFisher). Cells were infected with ˜0.1 plaque-forming units per cell and then incubated for about 24 h before the medium supernatant was harvested and clarified by centrifugation at 900×g for 30 m at room temperature. Clarified supernatants were overlaid on 20% sucrose cushions prepared in phosphate-buffered saline (PBS), then centrifuged for 2 hrs (18,000 rpm, 42,900 g, 4° C.) using a SW28 rotor (Beckman Coulter). The sucrose solution was aspirated completely from the virus pellet after which virus was suspended in Hank's Balanced Salt Solution (HBSS, ThermoFisher) containing 15% Trehalose (Life Sciences Advanced Technologies) that was adjusted to pH 7.2. Virus suspensions were stored at −80° C. in aliquots.
Pseudotyped VSVΔG-Env.BG505 was produced in VERO-CD4/CCR5 cells that were electroporated with plasmid expressing VSV G IND or NJ. In preparation for electroporation, cells were harvested and treated as described before (46) and were suspended in 0.7 ml of VCM2 (˜2×10 7 cells). Purified VSVΔG-Env.BG505 (0.1 pfu per cell) and 50 ug of pCMV-G expression plasmid was added to the cell suspension before performing electroporation with the BTX ECM830 instrument. After electroporation, the cells were processed and transferred to one T175 flask per electroporation cuvette, after which they were cultured in VCM1 for 3-4 hours at 37° C. before performing heat shock (43° C.) for 3 hours (46). After heat shock, the cells were returned to 37° C. and allowed to recover for 2 h before the medium was removed and replaced VPSFM supplemented with 4 mM L-Glutamine. Incubation was continued 24-48 hours at 37° C. until cytopathic effect was evident throughout the culture after which virus was harvested and purified as described above.
VSV vector infectious units were quantified by plaque assay (16). For VSVΔG-Env.BG505, GHOST-CD4-CCR5 cell monolayers were used (NIH AIDS Reagent Program, Division of AIDS, NIAID, NIH, catalog number 3944, 55) while VERO cells were used for VSV-G6-Env.BG505. Near-confluent cell monolayers were infected with serially diluted virus before being overlaid with VCM3 containing 0.8% agarose. When plaques were visible, cells were fixed with 7% formaldehyde and stained with a solution of 7% crystal violet in water. Plaques were counted from duplicate wells and infectious titers were expressed as plaque-forming units (pfus) per ml.
Western blotting was used to confirm Env expression by infected cells and also to characterize purified VSV vector particles. For analysis of Env expression, cytoplasmic lysates were prepared from infected monolayers using CellLytic M reagent (Sigma). Lysate proteins were then subjected to denaturing SDS polyacrylamide gel electrophoresis (SDS PAGE) and transferred to nitrocellulose membranes. Proteins were detected with monoclonal antibodies or polyclonal serum specific for Env gp120.BG505 or VSV structural proteins. Secondary antibodies conjugated to horse-radish peroxidase and chemiluminescence detection was used to visualize specific bands. Protein composition of VSV vector particles was analyzed by Western blot using similar methods applied to virus purified by centrifugation through sucrose cushions.
VSV vector vaccine material was subjected to several tests to ensure the quality. Endotoxin levels were tested using the Endosafe Portable Test System (Charles River Laboratories, Boston). All vaccine lots had endotoxin levels less than 10 EU/ml. The absence of Mycoplasma was confirmed by PCR using the MycoSEQ® Mycoplasma Detection System (Life Technologies). Residual VERO cell DNA was less than 10 ng per dose as determined with the resDNASEQ® Vero Residual DNA Quantitation System (Life Technologies). Gene sequences were confirmed by nucleic acid sequencing as described before (16).
Vaccinations, SHIV Challenge, and Animal Care and Use.
Purpose-bred male Indian rhesus macaques were 4-7 years of age when they arrived at The State University of New York (SUNY) Downstate Medical Center, Division of Comparative Medicine. Animal care and use complied with The United States Department of Agriculture and The New York State Department of Health regulations. The SUNY Downstate Medical Center Institutional Animal Care and Use Committee reviewed all experimental procedures. Prior to receipt, all macaques were confirmed to be negative for Herpes B virus (BV), tuberculosis (TB), simian immunodeficiency virus (SIV), simian retrovirus (SRV), and simian T lymphotropic virus (STLV), as well as Shigella and Campylobacter jejuni.
No Macaques were included in the study if they were positive for MHC alleles Mamu-B*08 and B*17 associated with strong SIV replication control (56). Both groups vaccinated with VSV vectors each had 2 animals that were positive for Mamu-A*01 and two positive A*02, which have been associated with control of disease progression (56). The placebo control group also contained two animals that were positive for A*02 and one for A*01. For vaccination, macaques were sedated and positioned in dorsal recumbency after which vaccine was administered by the intraoral and intranasal routes. Vaccine or buffer control was administered by drops using a 1000 μl micropipette. 500 μl was delivered intranasally by alternating drops between the left and right nares, with time between drops allowed for the droplet to be inhaled. For intraoral, a total of 500 μl was administered by drops applied sublingually on the frenulum (250 μl) and to the anterior buccal surface of the inferior lip (250 μl) followed by 30-60 seconds of gentle massage to help distribute the inoculum. Animals were kept in dorsal recumbency throughout the procedure and were left in this position for an additional 5 minutes before being returned to their cages. Animals were singly housed for 48 h following all vaccinations, after which they were housed together (2-3 animals per cage) within the same vaccination group. Bedding material was analyzed for VSV genomes by qPCR and none was detected (data not shown).
Rectal challenge was performed using SHIV SF162p3 that was prepared in primary cultures of macaque PBMCs (34). The inoculum (total of 2.2×10 4 TCID50) consisted of virus in 1 ml of saline or RPMI medium. Sedated animals were positioned in sternal recumbency with the posterior elevated by placing an empty plastic container between the lower abdomen and the procedure table. Inoculation was performed by atraumatic insertion of a lightly lubricated 3 mL syringe approximately 5 cm into the rectum. The inoculum was slowly instilled over a one-minute period with the syringe left in place for and additional 4 minutes. After removing the syringe, macaques remained in sternal recumbency for 10 minutes. Challenged animals were caged separately for 48 h before being housed in groups of 2-3 within the same vaccination group.
SHIV infection was monitored by reverse transcription and quantitative PCR (RT-qPCR) using methods similar to those described earlier (57). Briefly, virus from 1.0 ml of plasma was collected by centrifugation at 25,000×g for 90 min (5° C.). The virus pellet was processed using the RNeasy Micro kit (Qiagen) by suspending virus in solution containing 300 μl of lysis buffer, 3 μl of 14.2 M 2-mercaptoethanol (Bio-Rad), and 16 μl of 20 mg/ml proteinase K (Qiagen). Samples were digested at 56° C. for 1 h, then RNA was purified using spin columns following the RNeasy Micro kit protocol. RNA was eluted in 50 μl of RNase-free water supplemented with 1 mM dithiothreitol (Sigma) and 1 U/μl RNAseOUT (Thermo Fisher Scientific) after which duplicate RT reactions were performed using 15 μl of purified RNA per reaction and 10 μl of a cocktail composed of reagents from the Sensiscript Reverse Transcriptase kit (Qiagen, Valencia, Calif., USA) including 1× reverse transcription buffer, 0.5 mM of each dNTP, 10 U/reaction RNase Inhibitor (Invitrogen, Carlsbad, Calif., USA), 10 Units Sensiscript Reverse transcriptase, and Gag-specific reverse primer (400 nM, 5′-CACTAGKTGTCTCTGCACTATPTGTTT-3′(SEQ ID NO: 4)) that annealed to the positive-sense genomic RNA. Reverse transcription was performed at 50° C. for 45 min and terminated by heat inactivation (95° C. for 2 min). The heat-inactivated 25-μl reaction was adjusted for qPCR by adding 30 μl of a reagent mix composed of 1× QuantiTect Multiplex PCR Master Mix (Qiagen), 400 nM of Gag-specific forward primer (5′-GTCTGCGTCATPTGGTGCAT-3′ (SEQ ID NO: 5)) and Gag-specific reverse primer, and 200 nM 6-carboxyfluorescein (FAM)-labeled minor groove binder (MGB) probe (5′-6FAM-CTTCPTCAGTKTGTTTCA-MGB-3′ (SEQ ID NO: 6)). A Stratagene Mx3005P Sequence Detection System was used for amplification and detection with the following conditions: 15 min at 95° C. followed by 45 cycles of 60 secs at 94° C. and 90 secs at 60° C. Results from duplicate test samples were averaged and genome copy numbers were interpolated from a curve generated with known RNA standards. Positive samples were defined as 200 genome copies per ml of plasma.
Analysis of Immune Responses.
To prepare plasma and peripheral blood mononuclear cells (PBMCs), blood was collected in tubes coated with sodium heparin. Plasma was prepared by removing cells by centrifugation and storage at −20° C. PBMCs were isolated by density gradient centrifugation on Ficoll Hypaque (GE Healthcare) in Accuspin tubes (Sigma-Aldrich) as described previously (57). Harvested PBMCs were suspended in Recovery Cell Culture Freezing Medium (Thermo Fisher Scientific) and stored in liquid nitrogen. Serum used for ELISA, Western blot procedures, binding antibody multiplex assays, or HIV pseudovirus neutralization assays was prepared from whole blood collected and processed in serum separator tubes (SST). Aliquots were stored at −20° C.
Intracellular cytokine staining was performed as described before (57). T cells were stimulated with Env.BG505 peptide (Genscript) 15-mers overlapping by 11 amino acids. Two different Env.BG505 peptide pools, spanning gp120 or gp41, were used at 4 μg per ml. All flow cytometry data had mock background responses subtracted.
Infected VERO and VERO-CD4/CCR5 cells and VSV vector particles also were analyzed by flow cytometry. For infected cells, VERO or VERO-CD4/CCR5 monolayers were infected with 0.1 to 1.0 pfu per cell and incubated overnight at 37°. The following day, cells were washed with PBS and then treated with Enzyme-free Cell Dissociation Buffer (Life Sciences) to produce a cell suspension. The cells were collected by centrifugation and then suspended in PBS before being incubated with Env-specific monoclonal antibodies. Flow cytometry was performed as described earlier (16).
Env incorporated in VSV particles also was analyzed by flow cytometry (16). Typically, purified virus (10 8 pfus) was bound to 100 ug Alum (Adju-Phos, Brenntag, Denmark) and the alum/virus complexes were blocked with PBS containing 3% BSA before being incubated with primary antibodies. After primary antibody incubation, the complexes were collected by centrifugation, washed using PBS containing 3% BSA, and then incubated with labeled secondary antibody. Centrifugation and washing was repeated before analysis with a LSRII flow cytometer (Becton Dickinson). The flow cytometer was set to analyze 30,000 particles with forward scatter (FSC) and side scatter (SSC) set to log 10 scale and threshold set to 4000. Data was analyzed using FlowJo software version 9.4 (Tree Star), where complexes were gated according to positivity compared to an alum only control.
Western blotting also was used for analysis of serum antibodies. Polypeptide substrates used for the analysis were either purified VSVΔG-EnvG.BG505 particles (no G pseudotype, 5×10 8 pfus) or purified Env proteins. Purified virus or protein was diluted to 162.5 μL in HBSS containing 15% Trehalose before being mixed with 62.5 μl LDS NuPAGE sample buffer (Novex) and 25 μL of NuPAGE Sample Reducing Agent (Novex). Samples were heat denatured before being electrophoresed in a denaturing preparative gel (NuPAGE 4-12% Bis-Tris 2D, ThermoFisher), and afterwards proteins were transferred to a nitrocellulose membrane. The membrane was rinsed with PBS and then incubated at room temperature for 1 h in blocking buffer composed of StartingBlock T20 buffer (ThermoFisher) supplemented with Clear Milk (Pierce/ThermoFisher) and 1% goat serum (Sigma). The blocked membrane was transferred to a multichannel Mini Protein II MultiScreen (BioRad) device that created multiple channels for analysis of sera from individual macaques. Individual lanes were incubated for 1 h at room temperature with heat-inactivated macaque serum (diluted 1:300 in blocking buffer for a total volume of 550 μL) before the solution was aspirated completely from each lane. The membrane was then removed from the multiscreen device and rinsed 5 times with miliQ water (59) and then washed 3 times for 5 minutes each with PBS containing 0.1% Tween-20. The membrane was incubated with secondary antibody (mouse anti-monkey IgG, SouthernBiotech; diluted 1:10,000 in blocking buffer) for 45 mins at room temperature after which it was washed as described above. The blot was developed with chemiluminescence reagent (SuperSignal West Femto Maximum Sensitivity Substrate, ThermoFisher) and imaged with a Biorad ChemiDoc Touch Imaging System.
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Example 3: Using VSV Evolution to Fine Tune the Env Immunogen
The EnvG hybrid was developed with the goal of producing an immunogen that was optimal for delivery with a live VSV vector. The Env-G design objectives were to generate a modified immunogen that enabled more abundant expression on the infected cell surface and increased incorporation in VSV particles while maintaining native Env antigenic properties and the ability to direct infection and replication in cells bearing the HIV coreceptors CD4 and CCR5 (CD4+/CCR5+ cells). Systematic evaluation of several Env domain substitutions demonstrated that replacement of the Env signal peptide (SP), transmembrane region (TM), and cytoplasmic tail (CT) with analogous domains from VSV G substantially improved expression of Env on the cell surface ( FIG. 1 ). Moreover, the surface of cells expressing the Env-G hybrid was bound by a panel of anti-Env monoclonal antibodies demonstrating that the antigenic profile was very similar to Env expressed by cells infected with HIV. Importantly, when a chimeric VSVΔG-Env vector was developed in which the G gene was replaced with Env-G, replication-competent recombinant virus was isolated that replicated specifically in CD4+/CCR5+ cells demonstrating that the EnvG retained functions that are essential for cell attachment and virus replication.
The domain swap approach enabled development of a live VSVΔG-Env chimera that readily propagated in CD4+/CCR5+ cells. After conducting multiple rounds of amplification in CD4+/CCR5+ cells, virus emerged that grew to higher titers suggesting that one or more mutations occurred resulting in a virus with increased replicative fitness. Genomic sequence analysis conducted on this virus strain identified three amino acid substitutions in Env, which were (amino acid numbering according to reference strain HXB2): K169T in the second variable domain of Env (V2 domain), I307T in the V3 domain, and W672R in the membrane-proximal external region (MPER). Consistent with these substitutions being the adaptive mutations that improve replicative fitness of the virus, the three amino acid changes have been stable during numerous subsequent rounds of virus propagation. Moreover, there was a substantial difference in virus quantities produced from infected cultures; VSVΔG-Env.BG505 with the three substitutions routinely exceeds 1×10e7 PFU per ml of medium while VSVΔG-Env.BG505 amplified prior to adaptation produced titers closer to 1×10e6.
To provide additional evidence that the three substitutions were the result of adaptive mutations that improved replicative fitness, the mutations were incorporated into the VSVΔG-Env.BG505 genomic DNA clone and a new recombinant virus was recovered containing the Env substitutions. This new recombinant strain grew efficiently, maintained the three amino acid substitutions during many rounds of propagation, and accrued no additional EnvG mutations. These results indicated that the three amino acid substitutions provided a replicative fitness advantage for the VSVΔG-Env.BG505 chimera.
The accrual of the three amino acid substitutions that enhanced replicate fitness indicated that EnvG structure likely required some additional ‘fine tuning’ to support optimal VSVΔG-Env.BG505 growth. The substitutions probably compensated for some structural changes in the Env complex that resulted from replacement of TM and CT with VSV G sequence. Structural changes in the Env complex are known to occur when mutations are introduced into the Env TM (1) and CT (2); thus, it is reasonable to expect that replacement of the Env TM and CT with VSV G sequence will cause some structural alteration that requires compensatory second-site mutations to achieve optimal EnvG function and virus replicative fitness.


The VSVΔG-Env.BG505 vaccine containing the K169T, I307T and W672R was found to be efficacious in the Indian Rhesus macaque SHIV challenge model.
CITATIONS


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Example 4: Transgenic Vero-CD4/CCR5 Cell Line
Human immunodeficiency virus (HIV) or its simian equivalent simian immunodeficiency virus (SIV) initiates infection through the viral envelope (Env) membrane glycoprotein binding to cellular CD4 and a coreceptor such as CCR5. Similarly, Env pseudotyped viral vectors can also infect cells by recognizing the coreceptors. In vitro, HIV, SIV, and Env pseudotyped replicating viral vectors can be propagated on primate peripheral blood mononuclear cells (PBMCs) or transgenic cell lines that are engineered to constitutively express CD4/CCR5. To support propagation and production of chimeric vesicular stomatitis virus (VSV) and canine distemper virus (CDV) vectors that have Env in place of native vector membrane glycoproteins, Applicants generated a transgenic Vero cell lines that express either human or rhesus macaque CD4/CCR5. Optimized transgene design and transfection procedures make transgenic Vero-CD4/CCR5 derivation process efficient and reliable. Stable clones were selected through rigorous multiple rounds of limiting dilutions. The VSV- and CDV-Env chimeras grow efficiently on the transgenic Vero-CD4/CCR5 cell lines and express Env of native conformation and antigenicity. Because Vero is a FDA-approved cell substrate for human vaccine production, the transgenic Vero-CD4/CCR5 cells have substantial potential to be used for manufacturing of replicating viral vectored HIV vaccines that express functional Env immunogens.
Most CD4/CCR5 expressing transgenic cell lines (e.g. GHOST, HOS, A3R5, and TZM-bl) were for use in analytical assays, but are not suitable for HIV vaccine manufacturing. The Vero cell line is approved for producing human vaccines (e.g. inactivated polio vaccine), therefore transgenic Vero-CD4/CCR5 cells are useful for HIV vaccine production since many safety risks associated with cell substrates have been addressed for the Vero cell background. In addition, the unique CD4/CCR5 transgene design directs strong expression of a CCR5 and CD4 polyprotein linked by a 2A sequence that is subsequently self-cleaved resulting in 1 to 1 ratio of CD4 and CCR5 molecules.
The transgenic Vero-CD4/CCR5 cell lines can be used for producing replicating viral vectors expressing HIV or SIV Env. Their use can also be expanded for use in assays requiring cells expressing CD4 and CCR5.
As the expression cassette proved effective with CD4 and CCR5, it is useful for making cell lines expressing other polypeptides.
FIGS. 33A-33E . Sequence annotation of VERO-hCD4/CCR5 gene. A restriction map of the Vert construct shows restriction enzymes cutting a maximum of two times, using RELibrary as a restriction enzyme library.
FIG. 34 . Gene design: VERO-CD4/CCR5 Cell Line(VERT). VERO-hCD4/CCR5: Transgenic Vero cells expression human CD4 and CCR5 receptors. sVERT3: Transgenic Vero cells expression simian CD4 and CCR5 receptors.
FIG. 35 . VERO-hCD4/CCR5 clone 4F11 resembles the Vero cell.
FIG. 36 . VERO-hCD4/CCR5 cytopathic effect when infected by VSV chimera.
FIG. 37 . VERO-hCD4/CCR5 maintains infectivity over 20 passages.
FIG. 38 . VERO-hCD4/CCR5 maintains the receptor expression over 20 passages.
Having thus described in detail preferred embodiments of the present invention, it is to be understood that the invention defined by the above paragraphs is not to be limited to particular details set forth in the above description as many apparent variations thereof are possible without departing from the spirit or scope of the present invention.