(en)Antibodies and antigen binding fragments that specifically binds to Siglec-15 are described herein. These antibodies or antigen binding fragments may have the ability of inhibiting differentiation of osteoclasts and/or the ability of inhibiting the bone resorption activity of osteoclasts. Compositions and cells expressing anti-Siglec-15 antibodies or antigen binding fragments are also disclosed herewith. Anti-Siglec-15 antibodies may also be useful for the treatment of bone loss, or bone diseases. Methods for the detection or diagnosis of bone loss or bone-related diseases are also described.

1.ApplicationNumber: US-201314406560-A
1.PublishNumber: US-9493562-B2
2.Date Publish: 20161115
3.Inventor: STUIBLE MATTHEW
TREMBLAY GILLES BERNARD
SULEA TRAIAN
MORAITIS ANNA N.
FILION MARIO

4.Inventor Harmonized: STUIBLE MATTHEW(CA)
TREMBLAY GILLES BERNARD(CA)
SULEA TRAIAN(CA)
MORAITIS ANNA N(CA)
FILION MARIO(CA)

5.Country: US
6.Claims:
(en)Antibodies and antigen binding fragments that specifically binds to Siglec-15 are described herein. These antibodies or antigen binding fragments may have the ability of inhibiting differentiation of osteoclasts and/or the ability of inhibiting the bone resorption activity of osteoclasts. Compositions and cells expressing anti-Siglec-15 antibodies or antigen binding fragments are also disclosed herewith. Anti-Siglec-15 antibodies may also be useful for the treatment of bone loss, or bone diseases. Methods for the detection or diagnosis of bone loss or bone-related diseases are also described.

7.Description:
(en)PRIORITY CLAIM
This patent application is a national stage filing under 35 U.S.C. §371 of international application No. PCT/CA2013/000646 filed on Jul. 17, 2013, which claimed priority to U.S. provisional application No. 61/673,442 filed Jul. 19, 2012, U.S. provisional application No. 61/777,049 filed on Mar. 12, 2013 and U.S. provisional application No. 61/810,415 filed on Apr. 10, 2013. The entire contents of each of these priority applications are incorporated herein by reference.
SEQUENCE LISTING
In accordance with 37 C.F.R. §1,52(e)(5), a Sequence Listing in the form of a text file (entitled “Sequence Listing”, created on Dec. 9, 2014 and of 168 kilobytes) is incorporated herein by reference in its entirety.


FIELD OF THE INVENTION
The present invention relates to antibodies and antigen binding fragments thereof that specifically bind to Siglec-15. The present invention particularly relates to anti-Siglec-15 antibodies adapted for administration to human and/or anti-Siglec-15 antibodies comprising amino acids of a human IgG1 constant region. The present invention also relates to the use of anti-Siglec-15 antibodies for treatment and/or diagnosis of diseases or conditions.
The antibodies of the present invention may be used, for example, to inhibit the activity or function of Siglec-15 or to deliver therapeutic agents to cells expressing the protein.
BACKGROUND OF THE INVENTION
Bone is a dynamic connective tissue comprised of functionally distinct cell populations required to support the structural, mechanical and biochemical integrity of bone and the human body's mineral homeostasis. The principal cell types involved include, osteoblasts responsible for bone formation and maintaining bone mass, and osteoclasts responsible for bone resorption. Osteoblasts and osteoclasts function in a dynamic process termed bone remodelling. The development and proliferation of these cells from their progenitors is governed by networks of growth factors and cytokines produced in the bone microenvironment as well as by systemic hormones. Bone remodelling is ongoing throughout the lifetime of the individual and is necessary for the maintenance of healthy bone tissue and mineral homeostasis. The process remains largely in equilibrium and is governed by a complex interplay of systemic hormones, peptides and downstream signalling pathway proteins, local transcription factors, cytokines, growth factors and matrix remodelling genes.
An interference or imbalance arising in the bone remodelling process can produce skeletal disease, with the most common skeletal disorders characterized by a net decrease in bone mass. A primary cause of this reduction in bone mass is an increase in osteoclast number and/or activity. The most common of such disease, and perhaps the best known, is osteoporosis occurring particularly in women after the onset of menopause. In fact osteoporosis is the most significant underlying cause of skeletal fractures in late middle-aged and elderly women. While estrogen deficiency has been strongly implicated as a factor in postmenopausal osteoporosis, there is longstanding evidence that remodelling is a locally controlled process being that it takes place in discrete packets throughout the skeleton as first described by Frost over forty years ago (Frost H. M. 1964).
Since bone remodelling takes place in discrete packets, locally produced hormones and enzymes may be more important than systemic hormones for the initiation of bone resorption and the normal remodelling process. Such local control is mediated by osteoblasts and osteoclasts in the microenvironment in which they operate. For example, osteoclasts attach to the bone matrix and form a separate compartment between themselves and the bone surface delimited by a sealing zone formed by a ring of actin surrounding the ruffled border. Multiple small vesicles transport enzymes toward the bone matrix and internalize partially digested bone matrix. The microenvironment within the sealing zone is rich with the presence of lysosomal enzymes and is highly acidic compared to the normal physiological pH of the body. The ruffled border membrane also expresses RANK, the receptor for RANKL, and macrophage-colony stimulating factor (MCSF) receptor, both of which are responsible for osteoclast differentiation, as well as the calcitonin receptor capable of rapidly inactivating the osteoclast (Baron, R. 2003).
In a complex pattern of inhibition and stimulation, growth hormone, insulin-like growth factor-1, the sex steroids, thyroid hormone, calciotrophic hormones such as PTH and prostaglandin E2, various cytokines, such as interleukin-1 beta, interleukin-6, and tumor necrosis factor-alpha, and 1,25-dihydroxyvitamin D (calcitriol) act coordinately in the bone remodelling process (Jilka et al. 1992; Poli et al. 1994; Srivastava et al. 1998; de Vemejoul 1996).
Thus, it stands to reason that the unique local environments created by these specialized cells is due to the expression of either unique genetic sequences not expressed in other tissues and/or splice variants of polynucleotides and polypeptides expressed in other tissues. The isolation and identification of polynucleotides, polypeptides and their variants and derivatives specific to osteoclast activity may permit a clearer understanding of the remodelling process and offer tissue specific therapeutic targets for the treatment of disease states related to bone remodelling.
Many diseases linked to bone remodelling are poorly understood, generally untreatable or treatable only to a limited extent. For example, osteoarthritis is difficult to treat as there is no cure and treatment focuses on relieving pain and preventing the affected joint from becoming deformed. Non-steroidal anti-inflammatory drugs (NSAIDs) are generally used to relieve pain.
Another example is osteoporosis where the only current medications approved by the FDA for use in the United States are the anti-resorptive agents that prevent bone breakdown. Estrogen replacement therapy is one example of an anti-resorptive agent. Others include alendronate (Fosamax—a biphosphonate anti-resorptive), risedronate (Actonel—a bisphosphonate anti-resorptive), raloxifene (Evista—selective estrogen receptor modulator (SERM)), calcitonin (Calcimar—a hormone), and parathyroid hormone/teriparatide (Forteo—a synthetic version of the human hormone, parathyroid hormone, which helps to regulate calcium metabolism).
Bisphosphonates such as alendronate and risedronate bind permanently to the surface of bone and interfere with osteoclast activity. This allows the osteoblasts to outpace the rate of resorption. The most common side effects are nausea, abdominal pain and loose bowel movements. However, alendronate is reported to also cause irritation and inflammation of the esophagus, and in some cases, ulcers of the esophagus. Risedronate is chemically different from alendronate and has less likelihood of causing esophagus irritation. However, certain foods, calcium, iron supplements, vitamins and minerals, or antacids containing calcium, magnesium, or aluminum can reduce the absorption of risedronate, thereby resulting in loss of effectiveness.
The most common side effect of Raloxifen and other SERMS (such as Tamoxifen) are hot flashes. However, Raloxifene and other hormone replacement therapies have been shown to increase the risk of blood clots, including deep vein thrombosis and pulmonary embolism, cardiovascular disease and cancer.
Calcitonin is not as effective in increasing bone density and strengthening bone as estrogen and the other anti-resorptive agents. Common side effects of either injected or nasal spray calcitonin are nausea and flushing. Patients can develop nasal irritations, a runny nose, or nosebleeds. Injectable calcitonin can cause local skin redness at the site of injection, skin rash, and flushing.
A situation demonstrative of the link between several disorders or disease states involving bone remodelling is that of the use of etidronate (Didronel) first approved by the FDA to treat Paget's disease. Paget's disease is a bone disease characterized by a disorderly and accelerated remodelling of the bone, leading to bone weakness and pain. Didronel has been used ‘off-label’ and in some studies shown to increase bone density in postmenopausal women with established osteoporosis. It has also been found effective in preventing bone loss in patients requiring long-term steroid medications (such as Prednisone or Cortisone). However, high dose or continuous use of Didronel can cause another bone disease called osteomalacia. Like osteoporosis, osteomalacia can lead to weak bones with increased risk of fractures. Because of osteomalacia concerns and lack of enough studies yet regarding reduction in the rate of bone fractures, the United States FDA has not approved Didronel for the treatment of osteoporosis.
Osteoporosis therapy has been largely focused on antiresorptive drugs that reduce the rate of bone loss but emerging therapies show promise in increasing bone mineral density instead of merely maintaining it or slowing its deterioration. The osteoporosis early stage pipeline consists largely of drug candidates in new therapeutic classes, in particular cathepsin K inhibitors, osteoprotegerin and calcilytics as well as novel bisphosphonates. Some of these are examples where novel drugs exploiting genomics programs are being developed based on a deeper understanding of bone biology and have the potential to change the face of treatment of bone disorders in the long term.
The present invention particularly relates to anti-Siglec-15 antibodies adapted for administration to human. The present invention also particularly relates to anti-Siglec-15 antibodies comprising amino acids of a human IgG1 constant region (e.g., including humanized, chimeric or non-humanized antibodies). In some instances, the antibodies and antigen binding fragments of the present invention may bind to an epitope which is unique to a human Siglec-15 protein and which is not found in a corresponding Siglec-15 protein of other species (e.g., not found in Siglec-15 orthologs or putative orthologs). In other instances, the antibodies and antigen binding fragments of the present invention may bind to an epitope that is common to a human Siglec-15 protein and a mouse Siglec-15 protein. Yet in other instances, the antibodies and antigen binding fragments of the present invention may bind to an epitope that is common to human Siglec-15 and other orthologs or putative orthologs (see for example, Angata et al., 2007).
The present invention describes the use of antibodies specific for Siglec-15 for the diagnosis, prognosis, and treatment (including prevention) of cancer or bone loss (e.g., severe or excessive bone loss associated with bone-related disease or associated with an increase in osteoclast differentiation or activity). In particular, the present invention relates to the use of anti-Siglec-15 antibodies for inhibiting the differentiation of osteoclasts and/or for inhibiting bone resorption. The present invention also relates to the use of these antibodies for diagnosis, prevention and treatment of various other types of diseases where the activity of osteoclasts is increased.
Sialic-acid-binding immunoglobulin-like lectins (Siglecs) are members of the immunoglobulin (Ig) superfamily that have the ability to interact with sialic acids (McMillan and Crocker, 2008; Crocker et al., 2007). There are several Siglec family members that all share specific structural features, in particular, displaying an amino-terminal V-set Ig domain that binds to sialic acid and a variable number of C2-set Ig domains. These membrane receptors are generally expressed in highly specific manners and many of the family members are expressed in hematopoietic cells (McMillan and Crocker, 2008). These proteins are thought to promote cell-cell interactions, mediate signalling, and regulate immune functions through the recognition of glycans (Crocker et al., 2007). Sialic acids are nine-carbon sugars typically located at the ends of complex glycoconjugates on the surface of cells. They can be attached to a wide variety of proteins and lipids (McMillan and Crocker, 2008).
Siglec-15 is one of the most recently described Siglec family members that have a high homology to Siglec-14 (Angata et al., 2007). These authors reported that it preferentially binds to sialyl Tn structure and that it interacts with DAP12 and DAP10. The functional significance of these interactions is not known but it was proposed that Siglec-15 probably harbors an activating function (Angata et al., 2007). Despite these preliminary insights into a potential role in mammals of Siglec-15, important advances in the understanding of the biological function of the protein were contributed when the sequence was identified as part of a screen to discover novel regulators of osteoclast differentiation (Sooknanan et al. 2007). In this patent application, it was revealed that attenuation of the Siglec-15 transcript by RNA interference in a mouse model of osteoclastogenesis resulted in significant reduction of differentiation of precursors in response to RANKL treatment. Similar results were disclosed in human osteoclasts. Furthermore, the studies presented in this disclosure also showed that the localization of Siglec-15 at the cell membrane was necessary for its function in osteoclast differentiation. Furthermore, a recent publication showed that the presence of sialic acid at the end of surface glycoconjugates was required for proper osteoclast differentiation and were probably important for the fusion of osteoclast precursor cells (Takahata et al., 2007). This last observation creates a direct functional link between sialic acid binding and the expression of Siglec-15 in differentiating osteoclasts and strongly suggested that Siglec-15 plays a role in the early differentiation program of osteoclast precursors.
Thus, the expression profile of Siglec-15, its strong inducibility during osteoclast differentiation, its localization at the surface of the membrane, and its structural features all contribute to the feasibility of targeting this protein at the cell surface with monoclonal antibodies. The only other example of monoclonal antibody-based therapy that target osteoclasts is denosumab, a human monoclonal antibody that is specific for RANKL (Ellis et al. 2008). The present invention relates to the use of anti-Siglec-15 antibodies or antigen binding fragments as blockers of osteoclast differentiation and/or bone resorption, in the detection or treatment of bone loss, especially in the context of bone-related diseases or in the context of increased osteoclast differentiation or activity. The present invention also relates to the use of antibodies or antigen binding fragments in the detection or treatment of cancer.
SUMMARY OF THE INVENTION
This invention relates to antibodies and antigen binding fragments as well as kits useful for the treatment (including prevention), detection and diagnosis of bone loss or cancer. Humanized anti-Siglec-15 antibodies are particularly contemplated.
The antibodies or antigen binding fragments of the present invention may be useful for the treatment of bone loss or bone resorption.
The antibodies and antigen binding fragments may also be particularly be useful for detection of differentiated osteoclast or osteoclast undergoing differentiation. The antibodies and antigen binding fragments may additionally be useful for detection of and diagnosis of bone loss. The antibodies or antigen binding fragment of the present invention may also be useful for treating bone loss.
The antibodies and antigen binding fragments may also be particularly useful for detection or diagnosis of cancer cells expressing Siglec-15 and particularly cancers having a high expression of Siglec-15. The antibodies and antigen binding fragments may further be particularly be useful for detection of ovarian cancer, renal cancer, cancer of the central nervous system, prostate cancer, melanoma, breast cancer, lung cancer or colon cancer. The antibodies or antigen binding fragment of the present invention may further be useful for treating ovarian cancer, renal cancer, cancer of the central nervous system, prostate cancer, melanoma, breast cancer, lung cancer or colon cancer.
The antibodies or antigen-binding fragment of the present invention may bind to amino acids 20 to 259 of Siglec-15 (SEQ ID NO.:2) or to a corresponding region of a Siglec-15 variant (e.g., a variant having at least 80% sequence identity with SEQ ID NO.:12 including, for example, SEQ ID NO.:4). More particularly the antibodies or antigen-binding fragment of the present invention may bind to amino acids 49 to 165 of Siglec-15 (SEQ ID NO.:2) or to a corresponding region of a Siglec-15 variant (e.g., a variant having at least 80% sequence identity with SEQ ID NO.:12 including, for example, SEQ ID NO.:4). The antibodies or antigen binding fragment of the present invention include those which may bind to an epitope unique to human Siglec-15 including, for example, an epitope comprising the arginine located at position 99 (R99) of SEQ ID NO.:2.
The antibody or antigen binding fragment may be capable of inhibiting an osteoclast differentiation activity of the polypeptide and/or bone resorption.
It is to be understood herein that antibodies that preferably bind human Siglec-15 over mouse Siglec-15 may be more effective at inhibiting differentiation or activity of human osteoclasts than mouse osteoclasts. An antibody that binds an epitope found in human Siglec-15 and not in mouse Siglec-15, may inhibit differentiation or activity of human osteoclasts and not that of mouse osteoclasts. The Siglec-15 protein of cynomolgus monkeys is very similar to that of the human Siglec-15 amino acids. Potency of anti-Siglec-15 antibodies may thus be tested in monkeys or using cells isolated from monkeys. Therefore, potency assays may be adapted depending on the specificity of the antibody (e.g., towards human, monkey and/or mouse Siglec-15).
In accordance with an embodiment of the invention, the antibody or antigen binding fragment may interfere with the ability of the polypeptide to promote osteoclast differentiation and/or bone resorption. In accordance with another embodiment of the invention, the antibody or antigen binding fragment may interfere with the ability of the polypeptide to promote tumor growth.
The antibody or antigen binding fragment of the present invention may be capable of interfering with (inhibiting) differentiation of an osteoclast precursor cell into a differentiated osteoclast.
In accordance with the present invention, the antibody or antigen binding fragment may be, for example, a polyclonal antibody, a monoclonal antibody, a chimeric antibody, a humanized antibody, a human antibody, a hybrid antibody or a fragment thereof.
Particular examples of antibodies encompassed by the present invention include antibodies having at least one immunoglobulin chain (light chain or heavy chain) comprising a humanized variable domain while the other variable domains may be non-humanized (e.g., mouse variable domain) resulting in a hybrid antibody. Other example of antibodies encompassed by the present invention includes antibodies having heavy and light immunoglobulin chains comprising a humanized variable domain.
Other particular embodiments of the present invention include a humanized antibody where non-human amino acids (e.g., one or more amino acids from the mouse antibody counterpart) have been reintroduced.
The present invention therefore provides a humanized antibody of a non-human parent antibody (e.g., mouse antibody) that is capable of specific binding to Siglec-15.
In one embodiment, a hybrid antibody or fragment thereof may comprise, for example, a light chain variable region of a non-human antibody and a heavy chain variable region of a humanized antibody.
In another embodiment, a hybrid antibody or fragment thereof may comprise, for example, a heavy chain variable region of a non-human antibody and a light chain variable region of a humanized antibody.
A humanized or hybrid antibody of the present invention may comprise a heavy chain variable region which may include non-human complementarity determining region amino acid residues and human framework region amino acid residues of a natural human antibody and a complementary light chain.
A humanized or hybrid antibody of the present invention may comprise a light chain variable region which may include non-human complementarity determining region amino acid residues and human framework region amino acid residues of a natural human antibody and a complementary heavy chain.
The term “hybrid antibody” refers to an antibody comprising at least one humanized or human heavy or light chain variable region (having affinity for Siglec-15) and at least one non-human heavy or light chain variable region (e.g. from a mouse, rat, rabbit).
The natural human antibody that is selected for humanization of the non-human parent antibody may comprise a variable region having a three-dimensional structure similar to that of (superimposable to) a (modeled) variable region of the non-human parent antibody. As such, the humanized or hybrid antibody has a greater chance of having a three-dimensional structure similar to that of the non-human parent antibody.
In accordance with the present invention, the human framework region amino acid residues of the humanized or hybrid antibody light chain are from a natural human antibody light chain framework region. The light chain framework region of the natural human antibody selected for humanization purposes, may have, for example, at least 70% identity with a light chain framework region of the non-human parent antibody. Preferably, the natural human antibody selected for humanization purposes may have the same or substantially the same number of amino acids in its light chain complementarity determining region to that of a light chain complementarity determining region of the non-human parent antibody.
In other embodiments of the invention, the human framework region amino acid residues of the humanized or hybrid antibody light chain are from a natural human antibody light chain framework region having at least 70, 75, 80, 85% identity (or more) with the light chain framework region of the non-human parent antibody.
Also in accordance with the present invention, the human framework region amino acid residues of the humanized or hybrid antibody heavy chain are from a natural human antibody heavy chain framework region having at least 70% identity with a heavy chain framework region of the non-human parent antibody. Preferably, the natural human antibody selected for humanization purposes may have the same or substantially the same number of amino acids in its heavy chain complementarity determining region to that of a heavy chain complementarity determining region of the non-human parent antibody.
In other embodiments of the invention, the human framework region amino acid residues of the humanized or hybrid antibody heavy chain are from a natural human antibody heavy chain framework region having at least 70, 75, 80, 85% identity with the heavy chain framework region of the non-human parent antibody.
In an embodiment of the invention, the heavy chain variable region of the humanized or hybrid antibody may thus comprise at least one non-human complementarity determining region.
Alternatively, in other embodiments of the invention, the heavy chain variable region of the humanized or hybrid antibody may comprise at least two non-human complementarity determining regions or even three non-human complementarity determining regions.
In an additional embodiment of the invention, the light chain variable region may comprise at least one non-human complementarity determining region.
Alternatively, in yet additional embodiments of the invention, the light chain variable region comprise at least two non-human complementarity determining regions or even three non-human complementarity determining regions.
The humanized antibody may thus advantageously comprise all six CDRs of the non-human antibody. In the case of a divalent humanized antibody, all twelve CDRs may be from the non-human antibody.
The constant region or fragment thereof may be from an IgG1, IgG2, IgG3, or IgG4 and especially from a human IgG1, IgG2, IgG3, or IgG4. In a more specific embodiment, the constant region may be from an IgG2 (e.g., human IgG2). In a preferred embodiment the constant region may be from an IgG1 (e.g., human IgG1).
The constant region of the light chain may be a lambda constant region or a kappa constant region.
Antigen binding fragments which may be particularly be useful include, for example, a FV (scFv), a Fab, a Fab′ or a (Fab′) 2 .
The antibody or antigen binding fragment may be produced in or from an isolated mammalian cell (other than an hybridoma cell) or in an hybridoma cell. An exemplary embodiment of an isolated mammalian cell is a human cell.
In an aspect of the invention, the antibody or antigen binding fragment of the present invention may interfere (inhibit) with the differentiation of a human osteoclast precursor cell into a differentiated human osteoclast.
In an exemplary embodiment, the antibody or antigen binding fragment of the present invention may interfere (inhibit) with the differentiation of a primary human osteoclast precursor cell into a differentiated human osteoclast.
The antibodies and antigen binding fragments of the present invention may also be used to generally target cells expressing or overexpressing Siglec-15, including bone cells and breast, colon, lung, ovarian, prostate, and renal cancer cells as well as melanoma cells and cancer cells of the central nervous system.
More particularly, the antibodies and antigen binding fragments may be used to target osteoclasts cells undergoing differentiation.
The present invention provides in one aspect thereof, an antibody or antigen binding fragment (e.g., isolated or substantially purified) which may be capable of specific binding to SEQ ID NO:2.
As such, the present invention encompasses diagnostic and/or therapeutic antibodies or antigen binding fragments having specificity for SEQ ID NO:2. Also encompassed by the present invention are antibodies or antigen binding fragments having the same epitope specificity as the antibody of the present invention. A candidate antibody may be identified by determining whether it will bind to the epitope to which the antibodies described herein binds and/or by performing competition assays with antibodies or antigen binding fragments known to bind to the epitope.
Therefore, another aspect the present invention provides an isolated antibody or antigen binding fragment capable of competing with the antibody or antigen binding fragment described herein.
In further aspects, the present invention provides method of treatment and method of detection using the antibody or antigen binding fragment of the present invention.
The term “antibody” refers to intact antibody, monoclonal or polyclonal antibodies. The term “antibody” also encompasses, multispecific antibodies such as bispecific antibodies. Human antibodies are usually made of two light chains and two heavy chains each comprising variable regions and constant regions. The light chain variable region comprises 3 CDRs, identified herein as CDRL1, CDRL2 and CDRL3 flanked by framework regions. The heavy chain variable region comprises 3 CDRs, identified herein as CDRH1, CDRH2 and CDRH3 flanked by framework regions.
The term “antigen-binding fragment”, as used herein, refers to one or more fragments of an antibody that retain the ability to bind to an antigen (e.g., SEQ ID NO:2 or variants thereof). It has been shown that the antigen-binding function of an antibody can be performed by fragments of an intact antibody. Examples of binding fragments encompassed within the term “antigen-binding fragment” of an antibody include (i) a Fab fragment, a monovalent fragment consisting of the V L , V H , C L and C H1 domains; (ii) a F(ab′) 2 fragment, a bivalent fragment comprising two Fab fragments linked by a disulfide bridge at the hinge region; (iii) a Fd fragment consisting of the V H and C H1 domains; (iv) a Fv fragment consisting of the V L and V H domains of a single arm of an antibody, (v) a dAb fragment (Ward et al., (1989) Nature 341:544-546), which consists of a V H domain; and (vi) an isolated complementarity determining region (CDR), e.g., V H CDR3. Furthermore, although the two domains of the Fv fragment, V L and V H , are coded for by separate genes, they can be joined, using recombinant methods, by a synthetic linker that enables them to be made as a single polypeptide chain in which the V L and V H regions pair to form monovalent molecules (known as single chain Fv (scFv); see e.g., Bird et al. (1988) Science 242:423-426; and Huston et al. (1988) Proc. Natl. Acad. Sci. USA 85:5879-5883). Such single chain antibodies are also intended to be encompassed within the term “antigen-binding fragment” of an antibody. Furthermore, the antigen-binding fragments include binding-domain immunoglobulin fusion proteins comprising (i) a binding domain polypeptide (such as a heavy chain variable region, a light chain variable region, or a heavy chain variable region fused to a light chain variable region via a linker peptide) that is fused to an immunoglobulin hinge region polypeptide, (ii) an immunoglobulin heavy chain CH2 constant region fused to the hinge region, and (iii) an immunoglobulin heavy chain CH3 constant region fused to the CH2 constant region. The hinge region may be modified by replacing one or more cysteine residues with serine residues so as to prevent dimerization. Such binding-domain immunoglobulin fusion proteins are further disclosed in US 2003/0118592 and US 2003/0133939. These antibody fragments are obtained using conventional techniques known to those with skill in the art, and the fragments are screened for utility in the same manner as are intact antibodies.
A typical antigen binding site is comprised of the variable regions formed by the pairing of a light chain immunoglobulin and a heavy chain immunoglobulin. The structure of the antibody variable regions is very consistent and exhibits very similar structures. These variable regions are typically comprised of relatively homologous framework regions (FR) interspaced with three hypervariable regions termed Complementarity Determining Regions (CDRs). The overall binding activity of the antigen binding fragment is often dictated by the sequence of the CDRs. The FRs often play a role in the proper positioning and alignment in three dimensions of the CDRs for optimal antigen binding.
Antibodies and/or antigen binding fragments of the present invention may originate, for example, from a mouse, a rat or any other mammal or from other sources such as through recombinant DNA technologies.
The antibodies or antigen binding fragments may have therapeutic uses in the treatment of bone loss.
Hormone ablative therapy (treatment with drugs that stop the production of specific hormones) increases the risk of fractures due to bone loss. Adjuvant hormonal therapies for women with breast cancer involve antiestrogens (e.g., tamoxifen) and aromatase inhibitors, which have been shown to accelerate bone loss and increase fracture risk due to estrogen suppression. Additionally, many men with prostate cancer are treated with androgen deprivation therapy (ADT) (e.g., gonadotropin-releasing hormone [GnRH] agonists) as their cancer progresses. GnRH agonists inhibit production of testosterone, which acts as a growth factor for prostate cancer cells. However, this treatment also leads to a decrease in bone mass, thus increasing the risk of fractures due to osteoporosis. Therefore, the antibodies or antigen binding fragment of the present invention may have therapeutic uses in the treatment of bone loss associated with cancer treatment.
The antibodies or antigen binding fragments may also have therapeutic uses in the treatment of cancer. In an exemplary embodiment, the antibodies or fragments may have therapeutic uses in cancer treatment-induced bone loss. In another exemplary embodiment, the antibodies or fragments may have therapeutic uses in bone loss associated with bone diseases such as conditions where there is an increase in the bone degradative activity of osteoclasts. In certain instances, the antibodies or antigen binding fragments may interact with cells that express SEQ ID NO:2 and induce an immunological reaction by mediating ADCC. In other instances, the antibodies and fragments may block the interaction of SEQ ID NO:2 with its natural ligands. In yet other instances, the antibodies and fragment may induce internalization of the protein and/or its degradation.
The antibody or antigen binding fragment of the invention may be administered (e.g., concurrently, sequentially) with another drug useful for the treatment of bone loss, bone resorption or useful for the treatment of a disease associated with bone loss or bone resorption.
Antibodies and antigen binding fragment capable of inhibiting bone loss have been described in international application Nos. PCT/CA2010/001586 published under No. WO2011/041894 on Apr. 14, 2011, and PCT/CA2007/000210 published under No. WO2007/093042 on Feb. 13, 2007, the entire content of which is incorporated herein by reference.
Antibody Conjugates
Although it is not always necessary, for detection or therapeutic purposes, the antibody or antigen binding fragment of the present invention may be conjugated with a detectable moiety (i.e., for detection or diagnostic purposes) or with a therapeutic moiety (for therapeutic purposes).
For detection purposes, an unconjugated antibody (primary antibody) may be used for binding to the antigen and a secondary antibody carrying a detectable moiety and capable of binding to the primary antibody may be added. However, as indicated above, the anti-SIGLEC 15 antibody may be conjugated with a detectable label and as such a secondary antibody may not be necessary,
A “detectable moiety” is a moiety detectable by spectroscopic, photochemical, biochemical, immunochemical, chemical and/or other physical means. A detectable moiety may be coupled either directly and/or indirectly (for example via a linkage, such as, without limitation, a DOTA or NHS linkage) to antibodies and antigen binding fragments thereof of the present invention using methods well known in the art. A wide variety of detectable moieties may be used, with the choice depending on the sensitivity required, ease of conjugation, stability requirements and available instrumentation. A suitable detectable moiety include, but is not limited to, a fluorescent label, a radioactive label (for example, without limitation, 125I, In 111 , Tc 99 , I 131 and including positron emitting isotopes for PET scanner etc), a nuclear magnetic resonance active label, a luminescent label, a chemiluminescent label, a chromophore label, an enzyme label (for example and without limitation horseradish peroxidase, alkaline phosphatase, etc.), quantum dots and/or a nanoparticle. Detectable moiety may cause and/or produce a detectable signal thereby allowing for a signal from the detectable moiety to be detected.
In another exemplary embodiment of the invention, the antibody or antigen binding fragment thereof may be coupled (modified) with a therapeutic moiety (e.g., drug, cytotoxic moiety).
In some instances, for therapeutic purposes, an unconjugated antibody may by itself be capable of sequestering the antigen, may block an important interaction between the antigen and another binding partner, may recruit effector cells, etc. However, as indicated above, the antibody may be conjugated with a therapeutic moiety.
In an exemplary embodiment, the antibodies and antigen binding fragments may comprise a chemotherapeutic or cytotoxic agent. For example, the antibody and antigen binding fragments may be conjugated to the chemotherapeutic or cytotoxic agent. Such chemotherapeutic or cytotoxic agents include, but are not limited to, Yttrium-90, Scandium-47, Rhenium-186, Iodine-131, Iodine-125, and many others recognized by those skilled in the art (e.g., lutetium (e.g., Lu 177 ), bismuth (e.g., Bi 213 ), copper (e.g., Cu 67 )). In other instances, the chemotherapeutic or cytotoxic agent may be comprised of, among others known to those skilled in the art, 5-fluorouracil, adriamycin, irinotecan, auristatins, taxanes, pseudomonas endotoxin, ricin, calicheamicin and other toxins. Exemplary cytotoxic agents may particularly comprise an agent, which is capable of killing non-proliferating cells.
The antibody or antigen binding fragment of the present invention may especially be conjugated with agents targeting DNA. Exemplary embodiments of agents targeting DNA includes for example, alkylating agents such as duocarmycins and duocarmycin derivatives such as adozelesin, bizelesin, carzelesin etc. Other exemplary embodiments of agents targeting DNA includes for example, calicheamicin, esperamicin and derivatives (see compounds disclosed for example in U.S. Pat. Nos. 5,264,586, 5,108,192, 4,970,198, 5,037,651, 5,079,233, 4,675,187, 4,539,203, 4,554,162, 4,837,206 and US2007213511, the entire content of each document is incorporated herein by reference).
A particular embodiment of the invention includes for example, an antibody or antigen binding fragment disclosed herein conjugated with duocarmycin. Another particular embodiment of the invention includes for example, an antibody or antigen binding fragment disclosed herein conjugated with calicheamicin.
Alternatively, in order to carry out the methods of the present invention and as known in the art, the antibody or antigen binding fragment of the present invention (conjugated or not) may be used in combination with a second molecule (e.g., a secondary antibody, etc.) which is able to specifically bind to the antibody or antigen binding fragment of the present invention and which may carry a desirable detectable, diagnostic or therapeutic moiety.
Pharmaceutical Compositions of the Antibodies and their Use
Pharmaceutical compositions of the antibodies (conjugated or not) are also encompassed by the present invention. The pharmaceutical composition may comprise an antibody or an antigen binding fragment and may also contain a pharmaceutically acceptable carrier.
Other aspects of the invention relate to a composition which may comprise the antibody or antigen binding fragment described herein and a carrier.
Yet other aspects of the invention relate to the use of the isolated antibody or antigen binding fragment described herein in the treatment or diagnosis of bone diseases or cancer.
In addition to the active ingredients, a pharmaceutical composition may contain pharmaceutically acceptable carriers comprising water, PBS, salt solutions, gelatins, oils, alcohols, and other excipients and auxiliaries that facilitate processing of the active compounds into preparations that may be used pharmaceutically. In other instances, such preparations may be sterilized.
As used herein, “pharmaceutical composition” usually comprises therapeutically effective amounts of the agent together with pharmaceutically acceptable diluents, preservatives, solubilizers, emulsifiers, adjuvant and/or carriers. A “therapeutically effective amount” as used herein refers to that amount which provides a therapeutic effect for a given condition and administration regimen. Such compositions are liquids or lyophilized or otherwise dried formulations and include diluents of various buffer content (e.g., Tris-HCl., acetate, phosphate), pH and ionic strength, additives such as albumin or gelatin to prevent absorption to surfaces, detergents (e.g., Tween 20, Tween 80, Pluronic F68, bile acid salts). Solubilizing agents (e.g., glycerol, polyethylene glycerol), anti-oxidants (e.g., ascorbic acid, sodium metabisulfite), preservatives (e.g., thimerosal, benzyl alcohol, parabens), bulking substances or tonicity modifiers (e.g., lactose, mannitol), covalent attachment of polymers such as polyethylene glycol to the protein, complexation with metal ions, or incorporation of the material into or onto particulate preparations of polymeric compounds such as polylactic acid, polyglycolic acid, hydrogels, etc, or onto liposomes, microemulsions, micelles, unilamellar or multilamellar vesicles, erythrocyte ghosts, or spheroplasts. Such compositions may influence the physical state, solubility, stability, rate of in vivo release, and rate of in vivo clearance. Controlled or sustained release compositions include formulation in lipophilic depots (e.g., fatty acids, waxes, oils). Also comprehended by the invention are particulate compositions coated with polymers (e.g., poloxamers or poloxamines). Other embodiments of the compositions of the invention incorporate particulate forms protective coatings, protease inhibitors or permeation enhancers for various routes of administration, including parenteral, pulmonary, nasal, oral, vaginal, rectal routes. In one embodiment the pharmaceutical composition is administered parenterally, paracancerally, transmucosally, transdermally, intramuscularly, intravenously, intradermally, subcutaneously, intraperitonealy, intraventricularly, intracranially and intratumorally.
Further, as used herein “pharmaceutically acceptable carrier” or “pharmaceutical carrier” are known in the art and include, but are not limited to, 0.01-0.1 M or 0.05 M phosphate buffer or 0.8% saline. Additionally, such pharmaceutically acceptable carriers may be aqueous or non-aqueous solutions, suspensions, and emulsions. Examples of non-aqueous solvents are propylene glycol, polyethylene glycol, vegetable oils such as olive oil, and injectable organic esters such as ethyl oleate. Aqueous carriers include water, alcoholic/aqueous solutions, emulsions or suspensions, including saline and buffered media. Parenteral vehicles include sodium chloride solution, Ringer's dextrose, dextrose and sodium chloride, lactated Ringer's orfixed oils. Intravenous vehicles include fluid and nutrient replenishers, electrolyte replenishers such as those based on Ringer's dextrose, and the like. Preservatives and other additives may also be present, such as, for example, antimicrobials, antioxidants, collating agents, inert gases and the like.
For any compound, the therapeutically effective dose may be estimated initially either in cell culture assays or in animal models such as mice, rats, rabbits, dogs, or pigs. An animal model may also be used to determine the concentration range and route of administration. Such information may then be used to determine useful doses and routes for administration in humans. These techniques are well known to one skilled in the art and a therapeutically effective dose refers to that amount of active ingredient that ameliorates the symptoms or condition. Therapeutic efficacy and toxicity may be determined by standard pharmaceutical procedures in cell cultures or with experimental animals, such as by calculating and contrasting the ED 50 (the dose therapeutically effective in 50% of the population) and LD 50 (the dose lethal to 50% of the population) statistics. Any of the therapeutic compositions described above may be applied to any subject in need of such therapy, including, but not limited to, mammals such as dogs, cats, cows, horses, rabbits, monkeys, and humans.
The pharmaceutical compositions utilized in this invention may be administered by any number of routes including, but not limited to, oral, intravenous, intramuscular, intra-arterial, intramedullary, intrathecal, intraventricular, transdermal, subcutaneous, intraperitoneal, intranasal, enteral, topical, sublingual, or rectal means.
Pharmaceutical compositions of the present invention may further comprise for example, at least one drug member selected from the group consisting of bisphosphonates, active vitamin D3, calcitonin and derivatives thereof, hormone preparations such as estradiol, SERMs (selective estrogen receptor modulators), ipriflavone, vitamin K2 (menatetrenone), calcium preparations, PTH (parathyroid hormone) preparations, nonsteroidal anti-inflammatory agents, soluble TNF receptor preparations, anti-TNF-alpha antibodies or functional fragments of the antibodies, anti-PTHrP (parathyroid hormone-related protein) antibodies or functional fragments of the antibodies, IL-1 receptor antagonists, anti-IL-6 receptor antibodies or functional fragments of the antibodies, anti-RANKL antibodies or functional fragments of the antibodies and OCIF (osteoclastogenesis inhibitory factor).
The term “treatment” for purposes of this disclosure refers to both therapeutic treatment and prophylactic or preventative measures, wherein the object is to prevent or slow down (lessen) the targeted pathologic condition or disorder. Those in need of treatment include those already with the disorder as well as those prone to have the disorder or those in whom the disorder is to be prevented.
The antibodies or antigen binding fragments may have therapeutic uses in the treatment of various bone loss or cancer. In an exemplary embodiment, the antibodies or fragments may have therapeutic uses in bone loss associated with bone diseases such as conditions where there is an increase in the bone degradative activity of osteoclasts.
In certain instances, the anti-Siglec-15 antibodies and fragments may interact with cells, such as osteoclasts or osteoclast precursors, that express Siglec-15. In certain instances, the antibodies or antigen binding fragments may interact with cells that express SEQ ID NO:2 and induce an immunological reaction by mediating ADCC. In other instances, the antibodies and fragments may block the interaction of SEQ ID NO:2 with its natural ligands.
The anti-Siglec-15 antibodies or antigen binding fragments may have therapeutic uses in the treatment of bone loss in the context of various bone-related diseases, including but not limited to osteoporosis, osteopenia, osteomalacia, hyperparathyroidism, hypothyroidism, hyperthyroidism, hypogonadism, thyrotoxicosis, systemic mastocytosis, adult hypophosphatasia, hyperadrenocorticism, osteogenesis imperfecta, Paget's disease, Cushing's disease/syndrome, Turner's syndrome, Gaucher disease, Ehlers-Danlos syndrome, Marfan's syndrome, Menkes' syndrome, Fanconi's syndrome, multiple myeloma, hypercalcemia, hypocalcemia, arthritides, periodontal disease, rickets (including vitamin D dependent, type I and II, and x-linked hypophosphatemic rickets), fibrogenesis imperfecta ossium, osteosclerotic disorders such as pycnodysostosis and damage caused by macrophage-mediated inflammatory processes. In the preferred embodiment, the antibodies and fragments have therapeutic uses in conditions where severe bone loss prevails, in particular metastatic cancer to the bone.
The anti-Siglec-15 antibodies and antigen binding fragments thereof may have therapeutic uses in the treatment of cancer or bone loss caused by or associated with various bone remodelling disorders. In particular, the anti-Siglec-15 antibodies and immunologically functional fragments therein have therapeutic uses in conditions where osteoclasts are hyperactive and contribute to the degradation of the bone surface. In certain instances, the anti-Siglec-15 antibodies and antigen binding fragment thereof may be administered concurrently in combination with other treatments given for the same condition. As such, the antibodies may be administered with anti-resorptives (e.g., bisphosphonates) that are known to those skilled in the art. Additionally, the antibodies may be administered with anti-mitotics (e.g., taxanes), platinum-based agents (e.g., cisplatin), DNA damaging agents (e.g. Doxorubicin), and other cytotoxic therapies that are known to those skilled in the art. In other instances, the anti-Siglec-15 antibodies and immunologically functional fragments therein may be administered with other therapeutic antibodies. These include, but are not limited to, antibodies that target RANKL, EGFR, CD-20, and Her2.
Further scope, applicability and advantages of the present invention will become apparent from the non-restrictive detailed description given hereinafter. It should be understood, however, that this detailed description, while indicating exemplary embodiments of the invention, is given by way of example only, with reference to the accompanying drawings.



BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1A . Molecular model of the murine 25D8 variable domain. CDR loops are indicated with arrows as L1, L2 and L3 in the light chain and H1, H2 and H3 in the heavy chain.
FIG. 1B . Molecular model of the murine 25E9 variable domain. CDR loops are indicated with arrows as L1, L2 and L3 in the light chain and H1, H2 and H3 in the heavy chain.
FIG. 2A . Sequence alignment of the mouse, humanized and selected human framework sequences for the variable light (VL) domain of the 25D8 antibody. The CDRs are highlighted in light grey and correspond to SEQ ID NOs. 53, 54 and 55.
FIG. 2B . Sequence alignment of the mouse, humanized and selected human framework sequences for the variable heavy (VH) domain of the 25D8 antibody. The CDRs are highlighted in light grey and correspond to SEQ ID NOs. 56, 57 and 58.
FIG. 3A . Sequence alignment of the mouse, humanized and selected human framework sequences for the variable light (VL) domain of the 25E9 antibody. The CDRs are highlighted in light grey and correspond to SEQ ID NOs. 47, 48 and 49.
FIG. 3B . Sequence alignment of the mouse, humanized and selected human framework sequences for the variable heavy (VH) domain of the 25E9 antibody. The CDRs are highlighted in light grey and correspond to SEQ ID NOs. 50, 51 and 52.
FIG. 4A . Assembled sequences of the humanized full-length IgG2 25D8 (SEQ ID NOs.:23 and 27) and chimeric full-length IgG2 (SEQ ID NOs.:21 and 25) 25D8 antibodies.
FIG. 4B . Assembled sequences of the humanized full-length IgG2 25E9 (SEQ ID NOs.:7 and 29) and chimeric full-length IgG2 25E9 (SEQ ID NOs.:5 and 30) antibodies.
FIG. 5A . SPR chromatograms of the mouse and humanized 25D8 IgG2 antibodies.
FIG. 5B . SPR chromatograms of the mouse and humanized 25E9 IgG2 antibodies.
FIG. 6A illustrates the alignment between 25E9 mouse light chain variable domain and 25E9 humanized light chain variable domain Variant 1. Alignment were done by using the ClustalW2 program; where “*” means that the residues in that column are identical in all sequences in the alignment, “:” means that conserved substitutions have been observed and “.” means that semi-conserved substitutions are observed. (Larkin M. A., et al., (2007) ClustalW and ClustalX version 2 . Bioinformatics 2007 23(21): 2947-2948). These alignments were used to generate the consensus sequences set forth in SEQ ID NOs.: 33, 34 and 35.
FIG. 6B illustrates the alignment between 25E9 mouse heavy chain variable domain and 25E9 humanized heavy chain variable domain Variant 1. Alignment were done by using the ClustalW2 program; where “*” means that the residues in that column are identical in all sequences in the alignment, “:” means that conserved substitutions have been observed and “.” means that semi-conserved substitutions are observed. (Larkin M. A., et al., (2007) ClustalW and ClustalX version 2 . Bioinformatics 2007 23(21): 2947-2948). These alignments were used to generate the consensus sequences set forth in SEQ ID NOs. 36, 37 and 38.
FIG. 7A illustrates the alignment between 25D8 mouse light chain variable domain and 25D8 humanized light chain variable domain. Alignment were done by using the ClustalW2 program; where “*” means that the residues in that column are identical in all sequences in the alignment, “:” means that conserved substitutions have been observed and “.” means that semi-conserved substitutions are observed. (Larkin M. A., et al., (2007) ClustalW and ClustalX version 2 . Bioinformatics 2007 23(21): 2947-2948). These alignments were used to generate the consensus sequences set forth in SEQ ID NOs.: 39, 40 and 41.
FIG. 7B illustrates the alignment between 25D8 mouse heavy chain variable domain and 25D8 humanized heavy chain variable domain. Alignment were done by using the ClustalW2 program; where “*” means that the residues in that column are identical in all sequences in the alignment, “:” means that conserved substitutions have been observed and “.” means that semi-conserved substitutions are observed. (Larkin M. A., et al., (2007) ClustalW and ClustalX version 2 . Bioinformatics 2007 23(21): 2947-2948). These alignments were used to generate the consensus sequences set forth in SEQ ID NOs.:42, 43 and 44.
FIG. 8 . Flow cytometry results indicating that 25E9 specifically binds to human Siglec-15 expressed on the surface of cells in a concentration dependent manner.
FIG. 9 . Images showing the ability of 25E9 to inhibit the differentiation and resorptive activity of human osteoclasts.
FIG. 10A . Western blot showing internalization of biotinylated Siglec-15 in the presence of anti-Siglec-15 antibody.
FIG. 10B . Characterization of Siglec-15 endocytosis by confocal microscopy.
FIG. 10C . Western blot showing Siglec-15 protein levels
FIG. 10D . Western blot showing Siglec-15 protein expression in RAW264.7 following RANKI stimulation in the presence or absence of anti-Siglec-15 antibody.
FIG. 11 . Analysis of cell signaling induced by Siglec-15 clustering. Control (C) or differentiated (Δ) RAW264.7 cells were treated with primary antibody (anti-Siglec-15 or control human IgG) at 4 C followed by a secondary crosslinking antibody for the indicated times at 37 C. Total lysates were analyzed by western blotting with the indicated antibodies.
FIG. 12 . SPR chromatograms illustrating the differences in binding parameters between the humanized 25E9 L1H1 IgG1 (left panel) and the humanized 25E9 L1H1 IgG2 (right panel). Purified Fc-Siglec-15 was immobilized (150RU) and humanized 25E9 was injected at the indicated concentrations (100 nM, 33.3 nM, 11.1 nM, 3.70 nM and 1.23 nM). The curves were fit with a 1:1 ratio.
FIG. 13 . Representative images showing the increased potency of the humanized 25E9 L1H1 IgG1 compared to the humanized 25E9 IgG2 for inhibiting the differentiation of osteoclasts.
FIG. 14A . Assembled sequences of the humanized full-length IgG1 25D8 (SEQ ID NOs.:23 and 46) and chimeric full-length IgG1 25D8 (SEQ ID NO.: 21 and 45) antibodies.
FIG. 14B . Assembled sequences of the humanized full-length IgG1 25E9 (SEQ ID NOs:7 and 13) and chimeric full-length IgG1 25E9 (SEQ ID NOs.:5 and 11) antibodies.
FIG. 15 . Flow cytometry results indicating that 25E9-ADC specifically binds to human Siglec-15 expressed on the surface of cells in a manner very similar to the unconjugated antibody.
FIG. 16 . Shows the survival curves of the 25E9-ADC against mature, multi-nucleated osteoclasts. The response is very different to the unconjugated 25E9, which strongly inhibits osteoclast activity without affecting their survival.
FIG. 17 Shows images of TRAP stained osteoclasts to illustrate the cytotoxic effects of the 25E9-ADC against mature, multi-nucleated osteoclasts. The response is very different to the unconjugated 25E9, which strongly inhibits osteoclast activity without affecting their survival. A control-ADC has no effect against osteoclasts.



DETAILED DESCRIPTION OF THE INVENTION
Variant antibodies or antigen binding fragments encompassed by the present invention are those, which may comprise an insertion, a deletion or an amino acid substitution (conservative or non-conservative). These variants may have at least one amino acid residue in its amino acid sequence removed and a different residue inserted in its place.
Sites of interest for substitutional mutagenesis include the hypervariable regions (CDRs), but modifications in the framework region or even in the constant region are also contemplated. Conservative substitutions may be made by exchanging an amino acid (of a CDR, variable chain, antibody, etc.) from one of the groups listed below (group 1 to 6) for another amino acid of the same group.
Generally, mutations in the CDRs may have a greater impact on the antigen binding activity of the antibody or antigen binding fragment than mutations in the framework region. Mutation in the framework region may be performed to increase the “humanness” of the antibody. Variant antibody or antigen binding fragments that are encompassed by the present invention are those which have a substantially identical antigen binding capacity (including similar, identical, or slightly less) to those presented herein or have a better antigen binding capacity than those presented herein.
Other exemplary embodiment of conservative substitutions are shown in Table 1A under the heading of “preferred substitutions”. If such substitutions result in a undesired property, then more substantial changes, denominated “exemplary substitutions” in Table 1A, or as further described below in reference to amino acid classes, may be introduced and the products screened.
It is known in the art that variants may be generated by substitutional mutagenesis and retain the biological activity of the polypeptides of the present invention. These variants have at least one amino acid residue in the amino acid sequence removed and a different residue inserted in its place. For example, one site of interest for substitutional mutagenesis may include a site in which particular residues obtained from various species are identical. Examples of substitutions identified as “conservative substitutions” are shown in Table 1A. If such substitutions result in a change not desired, then other type of substitutions, denominated “exemplary substitutions” in Table 1A, or as further described herein in reference to amino acid classes, are introduced and the products screened.
Substantial modifications in function or immunological identity are accomplished by selecting substitutions that differ significantly in their effect on maintaining (a) the structure of the polypeptide backbone in the area of the substitution, for example, as a sheet or helical conformation. (b) the charge or hydrophobicity of the molecule at the target site, or (c) the bulk of the side chain. Naturally occurring residues are divided into groups based on common side chain properties:
(group 1) hydrophobic: norleucine, methionine (Met), Alanine (Ala), Valine (Val), Leucine (Leu), Isoleucine (Ile) (group 2) neutral hydrophilic: Cysteine (Cys), Serine (Ser), Threonine (Thr) (group 3) acidic: Aspartic acid (Asp), Glutamic acid (Glu) (group 4) basic: Asparagine (Asn), Glutamine (Gln), Histidine (His), Lysine (Lys), Arginine (Arg) (group 5) residues that influence chain orientation: Glycine (Gly), Proline (Pro); and (group 6) aromatic: Tryptophan (Trp), Tyrosine (Tyr), Phenylalanine (Phe)

Non-conservative substitutions will entail exchanging a member of one of these classes for another.







TABLE 1A



Amino acid substitution






Original
Exemplary
Conservative
Semi-conservative

residue
substitution
substitution
substitution



Ala (A)
Val, Leu, Ile
Val
N, V, P, (C)

Arg (R)
Lys, Gln, Asn
Lys
S, T, E, D, A

Asn (N)
Gln, His, Lys, Arg,
Gln
K, R


Asp

Asp (D)
Glu, Asn
Glu
K, R, H, A

Cys (C)
Ser, Ala
Ser
F, G

Gln (Q)
Asn; Glu
Asn
M, L, K, R

Glu (E)
Asp, Gln
Asp
K, R, H, A

Gly (G)
Ala
Ala
—

His (H)
Asn, Gln, Lys, Arg,
Arg
L, M, A, (C)

Ile (I)
Leu, Val, Met, Ala,
Leu
F, Y, W, G, (C)


Phe,


norleucine

Leu (L)
Norleucine, Ile, Val,
Ile
F, Y, W, H, (C)


Met,


Ala, Phe

Lys (K)
Arg, Gln, Asn
Arg
Q, N, S, T, D, E, A

Met (M)
Leu, Phe, Ile
Leu
Q, F, Y, W, (C), (R),




(K), (E)

Phe (F)
Leu, Val, Ile, Ala,
Tyr
I, V, (C)


Tyr

Pro (P)
Ala
Ala
A, (C), (D), (E), F, H,




(K), L, M, N, Q, (R), S,




T, W, Y

Ser (S)
Thr
Thr
D, E, R, K

Thr (T)
Ser
Ser
D, E, R, K, I

Trp (W)
Tyr, Phe
Tyr
L, M, I, V, (C)

Tyr (Y)
Trp, Phe, Thr, Ser
Phe
L, M, I, V, (C)

Val (V)
Ile, Leu, Met, Phe,
Leu
P, (C)


Ala,


norleucine



Changing from A, F, H, I, L, M, P, V, W, or Y to C is semi-conservative if the cysteine remains as a free thiol. Changing from M to E, R, K is semi-conservative if the ionic tip of the new side group may reach the protein surface while the methylene groups make hydrophobic contact. Changing from P to one of K, R, E or D is semi-conservative if the side group is on or near the surface of the protein.



















































Variation in the amino acid sequence of the variant antibody or antigen binding fragment may include an amino acid addition, deletion, insertion, substitution etc., one or more modification in the backbone or side-chain of one or more amino acid, or an addition of a group or another molecule to one or more amino acids (side-chains or backbone).
Variant antibody or antigen binding fragment may have substantial sequence similarity and/or sequence identity in its amino acid sequence in comparison with that of the original antibody or antigen binding fragment amino acid sequence. The degree of similarity between two sequences is based upon the percentage of identities (identical amino acids) and of conservative substitution.
Generally, the degree of similarity and identity between variable chains has been determined herein using the Blast2 sequence program (Tatiana A. Tatusova, Thomas L. Madden (1999), “Blast 2 sequences—a new tool for comparing protein and nucleotide sequences”, FEMS Microbiol Lett. 174:247-250) using default settings, i.e., blastp program, BLOSUM62 matrix (open gap 11 and extension gap penalty 1; gapx dropoff 50, expect 10.0, word size 3) and activated filters.
Percent identity may therefore be indicative of amino acids which are identical in comparison with the original peptide and which may occupy the same or similar position.
Percent similarity may be indicative of amino acids which are identical and those which are replaced with conservative amino acid substitution in comparison with the original peptide at the same or similar position.
Variants (i.e., analogues) of the present invention (including VL variants, VH variants, CDR variants, antibody variants, polypeptide variants, etc.) therefore comprise those which may have at least 70%, 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% sequence identity with an original sequence or a portion of an original sequence.
In accordance with the present invention, a SEQ ID NO.:2 variant includes a polypeptide having a region at least 80% identical with amino acids 49-165 or with amino acids 20 to 259 of SEQ ID NO.:2. Variants of SEQ ID NO.:2 also include polypeptides having at least 80% sequence identity with SEQ ID NO.:2. Preferred variants of SEQ ID NO.:2 includes those that are able to inhibit osteoclast differentiation and/or bone resorption. Such variants may be identified, for example, by testing their osteoclast differentiation and/or bone resorption activity in vitro or in vivo. Examples of methods or assays that may be used to test the activity of Siglec-15 variants are described herein and have been provided in international application No. PCT/CA2007/001134. It is to be understood that the osteoclast used to perform the assays described herein may originate, for example, preferably from human but also from mouse. Preferred variants of SEQ ID NO.:2 may include, for example, those where an epitope comprising arginine 99 (R99) of SEQ ID NO.:2 is preserved.
Exemplary embodiments of variants are those having at least 81% sequence identity to a sequence described herein and 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% sequence similarity with an original sequence or a portion of an original sequence.
Other exemplary embodiments of variants are those having at least 82% sequence identity to a sequence described herein and 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% sequence similarity with an original sequence or a portion of an original sequence.
Further exemplary embodiments of variants are those having at least 85% sequence identity to a sequence described herein and 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% sequence similarity with an original sequence or a portion of an original sequence.
Other exemplary embodiments of variants are those having at least 90% sequence identity to a sequence described herein and 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% sequence similarity with an original sequence or a portion of an original sequence.
Additional exemplary embodiments of variants are those having at least 95% sequence identity to a sequence described herein and 95%, 96%, 97%, 98%, 99% or 100% sequence similarity with an original sequence or a portion of an original sequence.
Yet additional exemplary embodiments of variants are those having at least 97% sequence identity to a sequence described herein and 97%, 98%, 99% or 100% sequence similarity with an original sequence or a portion of an original sequence.
For a purpose of concision the applicant provides herein a Table 1B illustrating exemplary embodiments of individual variants encompassed by the present invention and comprising the specified % sequence identity and % sequence similarity. Each “X” is to be construed as defining a given variant.







TABLE 1B





Percent (%) sequence identity

























80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100




























Percent (%)
80
X





















sequence
81
X
X

similarity
82
X
X
X


83
X
X
X
X


84
X
X
X
X
X


85
X
X
X
X
X
X


86
X
X
X
X
X
X
X


87
X
X
X
X
X
X
X
X


88
X
X
X
X
X
X
X
X
X


89
X
X
X
X
X
X
X
X
X
X


90
X
X
X
X
X
X
X
X
X
X
X


91
X
X
X
X
X
X
X
X
X
X
X
X


92
X
X
X
X
X
X
X
X
X
X
X
X
X


93
X
X
X
X
X
X
X
X
X
X
X
X
X
X


94
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X


95
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X


96
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X


97
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X


98
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X


99
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X


100
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X
X












































As used herein, the term “identical” means that a sequence share 100% sequence identity with another sequence.
As used herein, the term “substantially identical” means that a sequence share 70%, 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% sequence identity with another sequence or a portion of another sequence.
The present invention encompasses CDRs, light chain variable domains, heavy chain variable domains, light chains, heavy chains, antibodies and/or antigen binding fragments which comprise at least 70% identity (including any range between 70% and 99%) with the sequence described herein.
The present invention relates to the use of monoclonal antibodies to target osteoclasts found in various bone related disease where severe bone loss is observed due to increased activity of the osteoclasts. In order to direct the antibodies to the osteoclasts, the identification of osteoclast-specific antigens that are expressed at the cell surface of the cells must be carried out. There are several technologies that are available to identify cell-specific antigens and the method that was used to identify Siglec-15 in differentiating osteoclasts that were treated with RANKL, an innovative discovery platform called Subtractive Transcription-based Amplification of mRNA (STAR), is described in the published patent application No. PCT/CA2007/000210.
Analysis of the human osteoclast STAR libraries yielded many genes that encode secreted and cell surface proteins. One of these, termed 0326-SL109, contained an open reading frame that encoded a polypeptide of 328 amino acids, corresponding to SEQ ID NO:2 that was encoded by a cDNA of 987 base pairs with the nucleotide sequence shown in SEQ ID NO:1. A search of publicly available databases revealed that the 0326-SL109 nucleotide sequence was identical to that of a human gene called CD33 antigen-like 3 (CD33L3). CD33L3 was later found to be a member of the Siglec family of sialic acid binding proteins and was renamed Siglec-15 based on homology to other Siglecs (Crocker et al., 2007). Based on this information, the mouse orthologue was isolated and sequenced and found to be approximately 85% identical to the human sequence at the amino acid level. SEQ ID NO:3 and SEQ ID NO:4 show the sequences of cDNA and polypeptide of the murine Siglec-15, respectively. Bioinformatic analysis predicted a type I membrane-anchored protein that presents its functional domain to the extracellular compartment. As with other Siglec sequences, an amino-terminal signal peptide (located between amino acids 1 and 19 of SEQ ID NO:2) targets the protein to the membrane of cells and the final processed protein is anchored to the membrane via a single transmembrane helix located at the carboxy-terminus (located between amino acids 261 and 283 of SEQ ID NO:2). The V-set Ig domain is located between amino acids 49 and 165 of SEQ ID NO:2 whereas the C2-set Ig domain is located between amino acids 178 and 244 of SEQ ID NO:2.
Previous findings (Sooknanan et al. 2007) established that the transcript encoding human Siglec-15 was significantly upregulated in response to RANKL. This determination was performed on RNA macroarrays that contained spotted total RNA samples from several different human osteoclast differentiation experiments from different human PBMNC donors. Furthermore, these studies (Sooknanan et al. 2007) revealed that the Siglec-15 transcript was expressed in only one normal tissue among a vast panel of 30 human normal tissues indicating a very high osteoclast specificity of the Siglec-15 gene expression. Using more sensitive methods such as semi-quantitative RT-PCR, the expression of the Siglec-15 mRNA was stimulated within one day of RANKL treatment in many osteoclast samples indicating that the gene was expressed early in osteoclast precursor cells, prior to the commencement of cell fusion. Finally, the tissue expression profile of Siglec-15 was assessed by semi-quantitative RT-PCR and found to only be expressed in a single normal human tissue thus validating the macroarray results of Sooknanan et al. Taken together, these expression results underscore the strength of the Applicant's discovery approach in its ability to identify targets, as exemplified by Siglec-15, that are highly restricted to differentiating osteoclasts.
Based on the expression of Siglec-15 in the early stages of differentiation of osteoclasts, its limited expression in normal tissues, and a critical biological role for Siglec-15 in the activity of osteoclasts, Siglec-15 was chosen as a therapeutic target for the development of monoclonal antibodies for the detection, prevention, and treatment of bone resorption or bone-related diseases such as cancer-induced bone loss, osteoporosis, bone loss associate with cancer treatment.
Therefore, a variety of anti-Siglec-15 antibodies and immunologically functional fragments thereof, such as chimeric and humanized monoclonal antibodies, antibody fragments, single chain antibodies, domain antibodies, and polypeptides with an antigen-binding region, for targeting Siglec-15 are provided.
In accordance with the present invention, the antibodies or antigen binding fragment thereof may particularly be able to inhibit osteoclast differentiation.
Further in accordance with the present invention, the antibodies or antigen binding fragment thereof may be able to inhibit osteoclast formation.
Also in accordance with the present invention, the antibodies or antigen binding fragment thereof may be able to inhibit osteoclasts activity.
Further in accordance with the present invention, the antibodies or antigen binding fragment thereof may be able to inhibit bone resorption (e.g., bone resorption activity of osteoclasts).
Accordingly, the present invention provides in one aspect, an antibody or antigen binding fragment thereof capable of specific binding to Siglec-15 which may have a light chain variable region at least 80% identical to SEQ ID NO.:6 and/or a heavy chain variable region at least 80% identical to SEQ ID NO.:12. The antibody or antigen binding fragment thereof may also comprise at least one amino acid substitution in comparison with SEQ ID NO.:6 or SEQ ID NO.:12.
The present invention also provides in another aspect, an antibody or antigen binding fragment thereof which may have a light chain variable region at least 80% identical to SEQ ID NO.:22 and/or a heavy chain variable region at least 80% identical to SEQ ID NO.:26. The antibody or antigen binding fragment thereof may also comprise at least one amino acid substitution in comparison with SEQ ID NO.:22 or SEQ ID NO.:26.
In accordance with the present invention, the amino acid substitution may be an amino acid appearing at a corresponding position in a natural human antibody.
In accordance with an embodiment of the invention, the amino acid substitution may be outside of a complementarity determining region (CDR).
In accordance with an embodiment of the invention, the antibody the amino acid substitution may be located, for example, in the light chain variable region.
In accordance with an additional embodiment of the invention, the antibody or antigen binding fragment thereof may comprise at least two or at least three amino acid substitutions. Such amino acid substitutions may be located in the same variable region or may be located in distinct variable regions.
Further in accordance with the present invention, the antibody or antigen binding fragment thereof may comprise for example, from one to twenty-five amino acid substitutions in the light chain variable region and/or heavy chain variable region. More particularly, the antibody or antigen binding fragment thereof may have, for example, from one to twenty-two amino acid substitution in its light chain variable region and from one to twenty-five amino acid substitutions in its heavy chain variable region.
Antibodies or antigen binding fragments comprising the complementarity determining regions of SEQ ID NO.:6 and the complementarity determining regions of SEQ ID NO.:12 and comprising framework amino acids of a human antibody are particularly contemplated, such as, for example, humanized antibody.
Antibodies or antigen binding fragments comprising the complementarity determining regions of SEQ ID NO.:22 and the complementarity determining regions of SEQ ID NO.:26 and comprising framework amino acids of a human antibody are particularly contemplated.
Exemplary embodiments of the invention includes for example an antibody or an antigen binding fragment thereof having a light chain variable domain as set forth in SEQ ID NO.:33 (Generic 25E9 light chain variable domain (consensus 1)).





(SEQ ID NO.: 33)

DIVMTQXXXSXPVTPGEXXSISCRSTKSLLHSNGNTYLYWXLQXPGQSPQ



LLIYRMSNLASGVPDRFSGSGSGTXFTLXISRVEAEDVGVYYCMQHLEYP



FTFGGGTKXEIK;













wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:6 (the mouse VL). The amino acid substitution may be, for example conservative or non-conservative. In accordance with the invention, the amino acid substitution may be conservative.
Another exemplary embodiment of the invention includes for example an antibody or an antigen binding fragment thereof having a light chain variable domain as set forth in SEQ ID NO.:34 (Generic 25E9 light chain variable domain (consensus 2)).





(SEQ ID NO.: 34)

DIVMTQX a1 X a2 X a3 SX a4 PVTPGEX a5 X a6 SISCRSTKSLLHSNGNTYL



YWX a7 LQX a8 PGQSPQLLIYRMSNLASGVPDRFSGSGSGTX a9 FTLX a10



ISRVEAEDVGVYYCMQHLEYPFTFGGGTKX a11 EIK;













wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:6 (the mouse VL) and;
wherein Xa1, Xa4, Xa7, Xa8, Xa10 and Xa11 may each independently be a conservative amino acid substitution in comparison with SEQ ID NO. 6;
wherein Xa2, Xa5, Xa6 may each independently be a semi-conservative amino acid substitution in comparison with SEQ ID NO. 6;
wherein Xa3 may be P or L; and
wherein Xa9 may be A or D.
Yet another exemplary embodiment of the invention includes for example, an antibody or an antigen binding fragment thereof having a light chain variable domain as set forth in SEQ ID NO.:35 (Generic 25E9 light chain variable domain (consensus 3)).





(SEQ ID NO.: 35)

DIVMTQX a1 X a2 X a3 SX a4 PVTPGEX a5 X a6 SISCRSTKSLLHSNGNTYL



YWX a7 LQX a8 PGQSPQLLIYRMSNLASGVPDRFSGSGSGTX a9 FTLX a10



ISRVEAEDVGVYYCMQHLEYPFTFGGGTKX a11 EIK;













wherein at least one of the amino acid identified by X (including Xa1 to Xa11) may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:6 (the mouse VL) and
wherein Xa1 may be A or S;
wherein Xa2 may be A or P;
wherein Xa3 may be P or L;
wherein Xa4 may be a hydrophobic amino acid (e.g., V or L);
wherein Xa5 may be S or P;
wherein Xa6 may be a hydrophobic amino acid (e.g., V or A);
wherein Xa7 may be an aromatic amino acid (e.g. F or Y);
wherein Xa8 may be a basic amino acid (e.g., R or K);
wherein Xa9 may be A or D;
wherein Xa10 may be a basic amino acid (e.g., R or K); and
wherein Xa11 may be a hydrophobic amino acid (e.g., L or V).
In a further embodiment, the present invention includes for example, an antibody or an antigen binding fragment thereof, having a heavy chain variable domain as set forth in SEQ ID NO.:36 (Generic 25E9 heavy chain variable domain (consensus 1)).





(SEQ ID NO.: 36)

EIQLQQSGXEXXXPGXSVXXSCKASGYTFTDYDMHVWXQXPXXGLEWXGT



IDPETGGTAYNQKFKGXXTXTADXSXXTAYMELSSLXSEDXAVYYCTSFY



YTYSNYDVGFAYWGQGTLVTVSX;













wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:12 (the mouse VH). The amino acid substitution may be, for example conservative or non-conservative. In accordance with the invention, the amino acid substitution may be conservative.
Yet a further embodiment of the present invention includes for example, an antibody or an antigen binding fragment thereof having a heavy chain variable domain as set forth in SEQ ID NO.:37 (Generic 25E9 heavy chain variable domain (consensus 2)).







(SEQ ID NO.: 37)


EIQLQQSGX b1 EX b2 X b3 X b4 PGX b5 SVX b6 X b7 SCKASGYTFTDYDMHW





VX b8 QX b9 PX b10 X b11 GLEWX b12 GTIDPETGGTAYNQKFKGX b13





X b14 TX b15 TADX b16 SX b17 X b18 TAYMELSSLX b19 SEDX b20 AVYYC





TSFYYTYSNYDVGFAYWGQGTLVTVSX b21 ;















wherein at least one of the amino acid identified by X (including Xb1 to Xb21) may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:12 (the mouse VH) and
wherein Xb2, Xb4, Xb5, Xb7, Xb8, Xb9, Xb11, Xb12, Xb13, Xb15, Xb16, Xb17, Xb18, Xb20 and Xb21 may each independently be a conservative amino acid substitution in comparison with SEQ ID NO. 12;
wherein Xb1, Xb6, Xb14 may each independently be a semi-conserved amino acid substitution in comparison with SEQ ID NO.:12 (the mouse VH);
wherein Xb3 may be V or K;
wherein Xb10 may be V or G; and
wherein Xb19 may be T or R.
Another embodiment of the invention includes, for example, an antibody or an antigen binding fragment having an heavy chain variable domain as set forth in SEQ ID NO.:38 (Generic 25E9 heavy chain variable domain (consensus 3)).







(SEQ ID NO.: 38)


EIQLQQSGX b1 EX b2 X b3 X b4 PGX b5 SVX b6 X b7 SCKASGYTFTDYDMHW





VX b8 QX b9 PX b10 X b11 GLEWX b12 GTIDPETGGTAYNQKFKGX b13





X b14 TX b15 TADX b16 SX b17 X b18 TAYMELSSLX b19 SEDX b20 AVYYC





TSFYYTYSNYDVGFAYWGQGTLVTVSX b21 ;















wherein at least one of the amino acid identified by X (including Xb1 to Xb21) may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:12 (the mouse VH) and;
wherein Xb1 may be a hydrophobic amino acid (e.g., V or A);
wherein Xb2 may be a hydrophobic amino acid (e.g., L or V);
wherein Xb3 may be V or K;
wherein Xb4 may be a basic amino acid (e.g., R or K);
wherein Xb5 may be A or S;
wherein Xb6 may be T or K;
wherein Xb7 may be a hydrophobic amino acid (e.g., L or V);
wherein Xb8 may be a basic amino acid (e.g., K or R);
wherein Xb9 may be T or A;
wherein Xb10 may be V or G;
wherein Xb11 may be a basic amino acid (e.g., H or Q);
wherein Xb12 may be a hydrophobic amino acid (e.g., I or M);
wherein Xb13 may be a basic amino acid (e.g., K or R);
wherein Xb14 may be a hydrophobic amino acid (e.g., A or V);
wherein Xb15 may be a hydrophobic amino acid (e.g., L or I);
wherein Xb16 may be a basic amino acid (e.g., R or K);
wherein Xb17 may be a neutral hydrophilic amino acid (e.g., S or T);
wherein Xb18 may be a neutral hydrophilic amino acid (e.g., T or S);
wherein Xb19 may be T or R;
wherein Xb20 may be a neutral hydrophilic amino acid (e.g., S or T); and
wherein Xb21 may be A or S.
Other exemplary embodiments of the invention include, for example, an antibody or an antigen binding fragment thereof, having a light chain variable domain set forth in SEQ ID NO.: 39 (Generic 25D8 light chain variable domain (consensus 1)).





(SEQ ID NO.: 39)

DIVMTQXXXSXPVTXGXXASISCRSSKSLLHSNGITYLYWYLQKPGQSPQ



LLIYQMSNLASGVPDRFSXSGSGTDFTLXISRVEAEDVGVYYCAQNLELP



YTFGGGTKXEIK;













wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:22 (the mouse VL). The amino acid substitution may be, for example conservative or non-conservative. In accordance with the invention, the amino acid substitution may be conservative.
Yet another exemplary embodiment of the invention includes, for example, an antibody or antigen binding fragment thereof, having a light chain variable domain set forth in SEQ ID NO.: 40 (Generic 25D8 light chain variable domain (consensus 2)).





(SEQ ID NO.: 40)

DIVMTQX c1 X c2 X c3 SX c4 PVTX c5 GX c6 X c7 ASISCRSSKSLLHSNGIT



YLYWYLQKPGQSPQLLIYQMSNLASGVPDRFSX c8 SGSGTDFTLX c9 ISR



VEAEDVGVYYCAQNLELPYTFGGGTKX c10 EIK;













wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:22 (the mouse VL) and
wherein Xc1, Xc3, Xc9 and Xc10 may each independently be a conservative amino acid substitution in comparison with SEQ ID NO.:22;
wherein Xc2, Xc7, Xc8 may each independently be a semi-conservative amino acid substitution in comparison with SEQ ID NO.: 22;
Wherein Xc4 may be N or L;
Wherein Xc5 may be L or P; and
Wherein Xc6 may be T or E.
An additional embodiment of the present invention includes for example, an antibody or antigen binding fragment thereof, having a light chain variable domain set forth in SEQ ID NO.: 41 (Generic 25D8 light chain variable domain (consensus 3)).





(SEQ ID NO.: 41)

DIVMTQX c1 X c2 X c3 SX c4 PVTX c5 GX c6 X c7 ASISCRSSKSLLHSNGIT



YLYWYLQKPGQSPQLLIYQMSNLASGVPDRFSX c8 SGSGTDFTLX c9 ISR



VEAEDVGVYYCAQNLELPYTFGGGTKX c10 EIK;













wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:22 (the mouse VL) and
Wherein Xc1 may be A or T;
Wherein Xc2 may be A or P;
Wherein Xc3 may be F or L;
Wherein Xc4 may be N or L;
Wherein Xc5 may be L or P;
Wherein Xc6 may be T or E;
Wherein Xc7 may be S or P;
Wherein Xc8 may be S or G;
Wherein Xc9 may be a basic amino acid (e.g., R or K); and
Wherein Xc10 may be a hydrophobic amino acid (e.g., L or V).
Yet an additional embodiment of the present invention includes for example, an antibody or antigen binding fragment thereof, having a heavy chain variable domain set forth in SEQ ID NO.: 42 (Generic 25D8 heavy chain variable domain (consensus 1)).





(SEQ ID NO.: 42)

QVQXQQXGAEXXKPGXSVKXSCKASGYTFTSYWMHWVXQXPGQGLEWXGL



INPSNARTNYNEKFNTXXTXTXDKSXSTAYMXLSSLXSEDXAVYYCARGG



DGDYFDYWGQGTTXTVSS;













wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:26 (the mouse VH). The amino acid substitution may be, for example conservative or non-conservative. In accordance with the invention, the amino acid substitution may be conservative.
In a further embodiment, the present invention includes for example, an antibody or antigen binding fragment thereof, having a heavy chain variable domain set forth in SEQ ID NO.: 43 (Generic 25D8 heavy chain variable domain (consensus 2)).







(SEQ ID NO.: 43)


QVQX d1 QQX d2 GAEX d3 X d4 KPGX d5 SVKX d6 SCKASGYTFTSYWM





HWVX d7 QX d8 PGQGLEWX d9 GLINPSNARTNYNEKFNTX d10 X d11





TX d12 TX d13 DKSX d14 STAYMX d15 LSSLX d16 SEDX d17 AVYYCAR





GGDGDYFDYWGQGTTX d18 TVSS;















wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:26 (the mouse VH) and;
wherein Xd1, Xd3, Xd5, Xd6, Xd7, Xd9, Xd10, Xd12, Xd14, Xd15, Xd17, Xd18 may each independently be a conservative amino acid substitution in comparison with SEQ ID NO.:26;
wherein Xd2, Xd11, Xd13, may each independently be a semi-conservative amino acid substitution in comparison with SEQ ID NO.:26;
wherein Xd4 may be V or K;
wherein Xd8 may be R or A; and;
wherein Xd16 may be T or R.
In yet a further embodiment, the present invention includes, for example, an antibody or antigen binding fragment thereof, having a heavy chain variable domain set forth in SEQ ID NO.: 44 (Generic 25D8 heavy chain variable domain (consensus 3)).







(SEQ ID NO.: 44)


QVQX d1 QQX d2 GAEX d3 X d4 KPGX d5 SVKX d6 SCKASGYTFTSYWM





HWVX d7 QX d8 PGQGLEWX d9 GLINPSNARTNYNEKFNTX d10 X d11





TX d12 TX d13 DKSX d14 STAYMX d15 LSSLX d16 SEDX d17 AVYYCAR





GGDGDYFDYWGQGTTX d18 TVSS;















wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:26 (the mouse VH) and;
wherein Xd1 may be a hydrophobic amino acid (e.g., V or L);
wherein Xd2 may be P or S;
wherein Xd3 may be a hydrophobic amino acid (e.g., L or V);
wherein Xd4 may be V or K;
wherein Xd5 may be A or S;
wherein Xd6 may be a hydrophobic amino acid (e.g., L or V);
wherein Xd7 may be a basic amino acid (e.g., K or R);
wherein Xd8 may be R or A;
wherein Xd9 may be a hydrophobic amino acid (e.g., I or M);
wherein Xd10 may be a basic amino acid (e.g., K or R);
wherein Xd11 may be a hydrophobic amino acid (e.g., A or V);
wherein Xd12 may be a hydrophobic amino acid (e.g., L or I);
wherein Xd13 may be a hydrophobic amino acid (V or A);
wherein Xd14 may be a neutral hydrophilic amino acid (e.g., S or T);
wherein Xd15 may be Q or E;
wherein Xd16 may be T or R.
wherein Xd17 may be a neutral hydrophilic amino acid (e.g., S or T); and
wherein Xd18 may be a hydrophobic amino acid (L or V).
The term “humanized antibody” encompasses fully humanized antibody (i.e., frameworks are 100% humanized) and partially humanized antibody (e.g., at least one variable domain contains one or more amino acids from a human antibody, while other amino acids are amino acids of a non-human parent antibody). Typically a “humanized antibody” contains CDRs of a non-human parent antibody (e.g., mouse, rat, rabbit, non-human primate, etc.) and frameworks that are identical to those of a natural human antibody or of a human antibody consensus. In such instance, those “humanized antibodies” are characterized as fully humanized. A “humanized antibody” may also contain one or more amino acid substitutions that have no correspondence to those of the human antibody or human antibody consensus. Such substitutions include, for example, back-mutations (e.g., re-introduction of non-human amino acids) that may preserve the antibody characteristics (e.g., affinity, specificity etc.). Such substitutions are usually in the framework region. A “humanized antibody” optionally also comprise at least a portion of a constant region (Fc) which is typically that of a human antibody. Typically, the constant region of a “humanized antibody” is identical to that of a human antibody.
Of course, any antibody, antigen binding fragment thereof or antibody portion (light chain or heavy chain variable regions), having an amino acid sequence identical to that described herein is encompassed by the present invention, irrelevant of whether it is obtained via humanization technology, hybridoma technology, transgenic mice technologies, or else.
It is to be understood herein that the framework amino acids of the antibodies of the present invention may be from 80% to 100% (e.g., 85 to 100%; 90 to 100%, 95 to 100%) identical to those of a natural human antibodies. Usually, when a framework amino acid is not identical to a corresponding amino acid of a natural antibody, such amino acid may remain identical to the original amino acid (e.g., a mouse amino acid).
As used herein the term “from one to twenty-five (1 to 25)” includes every individual values and ranges such as for example, 1, 2, 3, and up to 25; 1 to 25; 1 to 24, 1 to 23, 1 to 22, 1 to 21, 1 to 20, 1 to 19; 1 to 18; 1 to 17; 1 to 16; 1 to 15 and so on; 2 to 25, 2 to 24, 2 to 23, 2 to 22, 2 to 21, 2 to 20; 2 to 19; 2 to 18; 2 to 17 and so on; 3 to 25, 3 to 24, 3 to 23, 3 to 22, 3 to 21, 3 to 20; 3 to 19; 3 to 18 and so on; 4 to 25, 4 to 24, 4 to 23, 4 to 22, 4 to 21, 4 to 20; 4 to 19; 4 to 18; 4 to 17; 4 to 16 and so on; 5 to 25, 5 to 24, 5 to 23, 5 to 22, 5 to 21, 5 to 20; 5 to 19; 5 to 18; 5 to 17 and so on, etc.
Likewise, other ranges such as for example, “from one to twenty-two (1 to 22)” includes every individual values and ranges such as for example, 1, 2, 3, and up to 22; 1 to 22, 1 to 21, 1 to 20, 1 to 19, 1 to 18, 1 to 17, 1 to 16, 1 to 15; 1 to 14; 1 to 13; 1 to 12; 1 to 11; 1 to 10 and so on; 2 to 22, 2 to 21, 2 to 20, 2 to 19, 2 to 18, 2 to 17, 2 to 16, 2 to 15; 2 to 14; 2 to 13; 2 to 12 and so on; 3 to 22, 3 to 21, 3 to 20, 3 to 19, 3 to 18, 3 to 17, 3 to 16, 3 to 15; 3 to 14; 3 to 13 and so on; 4 to 22, 4 to 21, 4 to 20, 4 to 19, 4 to 18, 4 to 17, 4 to 16, 4 to 15; 4 to 14; 4 to 13; 4 to 12; 4 to 11 and so on; 5 to 22, 5 to 21, 5 to 20, 5 to 19, 5 to 18, 5 to 17, 5 to 16, 5 to 15; 5 to 14; 5 to 13; 5 to 12 and so on, etc.
In a more specific embodiment of the invention, the number of amino acid substitutions that may be made in a light chain variable region derived from SEQ ID NO.:6 may be for example, from 1 to 11 amino acid substitutions.
In yet a more specific embodiment of the invention, the number of amino acid substitutions that may be made in a heavy chain variable region derived from SEQ ID NO.:12 may be for example, from 1 to 21 amino acid substitutions. In some instances, when considering SEQ ID NO.:12, it may be useful to have at least three amino acid substitutions.
In a further more specific embodiment of the invention, the number of amino acid substitutions that may be made in a light chain variable region derived from SEQ ID NO.:22 may be for example, from 1 to 10 amino acid substitutions.
In yet a further more specific embodiment of the invention, the number of amino acid substitutions that may be made in a heavy chain variable region of SEQ ID NO.:26 may be for example, from 1 to 18 amino acid substitutions.
In accordance with an embodiment of the invention, the acid substitutions may be for example, in the light chain variable region.
In accordance with an embodiment of the invention, the amino acid substitutions may be for example, in the heavy chain variable region.
An antibody or antigen binding fragment may therefore have a light chain variable region having up to twenty-two amino acid substitutions in comparison with SEQ ID NO.:6 or SEQ ID NO.:22 and may have a heavy chain variable region having up to twenty-five amino acid substitutions in comparison with SEQ ID NO.:12 or SEQ ID NO.:26. It is to be understood herein that when the antibody or antigen binding fragment has two light chain variable regions and two heavy chain variable regions, each one of the light chain variable regions may independently have up to twenty amino acid substitutions and each one of the heavy chain variable regions may have up to twenty amino acid substitutions.
As discussed herein the amino acid substitutions may be conservative or non-conservative. In an exemplary embodiment the amino acid substitutions may be conservative.
It is to be understood herein that the antibody or antigen binding fragment of the invention may if desired have a light chain variable region and/or heavy chain variable region showing a deletion in comparison with SEQ ID NO.:6, SEQ ID NO.:12, SEQ ID NO.:22 and/or SEQ ID NO.:26. Such deletion may be found, for example, at an amino- or carboxy-terminus of the light chain variable region and/or heavy chain variable region.
Another exemplary embodiment of the antibody or antigen binding fragment of the present invention includes for example, an antibody or antigen binding fragment having a light chain variable region which may comprise at least 90 consecutive amino acids of any of SEQ ID NO.:33, SEQ ID NO.:34, SEQ ID NO.:35, SEQ ID NO.:8 or SEQ ID NO.:10.
As used herein the term “at least 90 consecutive amino acids of SEQ ID NO.:33” also includes the terms “at least 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, or at least 112 consecutive amino acids”. The term “at least 90 consecutive amino acids of SEQ ID NO.:33” encompasses any possible sequence of at least 90 consecutive amino acids found in SEQ ID NO.:33 and especially those sequences which include the 3 CDRs of SEQ ID NO.:33, such as, for example a sequence comprising amino acids 6 to 108, 5 to 109, 13 to 103, 14 to 111 of SEQ ID NO.:33 and so on.
As used herein the term “at least 90 consecutive amino acids of SEQ ID NO.:34” also includes the terms “at least 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, or at least 112 consecutive amino acids”. The term “at least 90 consecutive amino acids of SEQ ID NO.:34” encompasses any possible sequence of at least 90 consecutive amino acids found in SEQ ID NO.:34 and especially those sequences which include the 3 CDRs of SEQ ID NO.:34, such as, for example a sequence comprising amino acids 7 to 109, 12 to 104, 22 to 112, 18 to 112 of SEQ ID NO.:34 and so on.
The terms “at least 90 consecutive amino acids of SEQ ID NO.:35”, “at least 90 consecutive amino acids of SEQ ID NO.:8” or “at least 90 consecutive amino acids of SEQ ID NO.:10” have similar meanings.
In accordance with the present invention, the antibody or antigen binding fragment of the present invention may have, for example, a light chain variable region as set forth in SEQ ID NO.:8 or in SEQ ID NO.:10.
The antibody or antigen binding fragment of the invention includes (or further includes) for example, a heavy chain variable region which may comprise at least 90 consecutive amino acids of any of SEQ ID NOs.:36, 37, 38, 14, 16, 18 or 20.
As used herein the term “at least 90 consecutive amino acids of SEQ ID NO.:36” also includes the terms “at least 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, or at least 123 consecutive amino acids”. The term “at least 90 consecutive amino acids of SEQ ID NO.:36” encompasses any possible sequence of at least 90 consecutive amino acids found in SEQ ID NO.:36 and especially those sequences which include the 3 CDRs of SEQ ID NO.:36, such as, for example a sequence comprising amino acids 1 to 106, 2 to 112, 11 to 113, 7 to 102 of SEQ ID NO.:36 and so on.
As used herein the term “at least 90 consecutive amino acids of SEQ ID NO.:37” also includes the terms “at least 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117, 118, 119, 120, 121, 122 or at least 123 consecutive amino acids”. The term “at least 90 consecutive amino acids of SEQ ID NO.:37” encompasses any possible sequence of at least 90 consecutive amino acids found in SEQ ID NO.:37 and especially those sequences which include the 3 CDRs of SEQ ID NO.:37, for example a sequence comprising amino acids 6 to 109, 8 to 113, 1 to 102, 2 to 105 of SEQ ID NO.:37 and so on.
The terms “at least 90 consecutive amino acids of SEQ ID NO.:38”, “at least 90 consecutive amino acids of SEQ ID NO.:14, “at least 90 consecutive amino acids of SEQ ID NO.:16”, “at least 90 consecutive amino acids of SEQ ID NO.:18” or “at least 90 consecutive amino acids of SEQ ID NO.:20” have similar meanings.
In accordance with the present invention, the antibody or antigen binding fragment of the present invention may have, for example, a heavy chain variable region as set forth in SEQ ID NO.:14, 16, 18 or 20.
In accordance with the present invention the antibody or antigen binding fragment may comprise, for example,
a) a light chain variable region which may comprise at least 90 consecutive amino acids of SEQ ID NO.:33 and a heavy chain variable region which may comprise at least 90 consecutive amino acids of any of SEQ ID NO.:36, SEQ ID NO.:37, SEQ ID NO.:38, SEQ ID NO.:14, SEQ ID NO.:16, SEQ ID NO.:18 or SEQ ID NO.:20; b) a light chain variable region which may comprise at least 90 consecutive amino acids of SEQ ID NO.:34 and a heavy chain variable region which may comprise at least 90 consecutive amino acids of any of SEQ ID NO.:36, SEQ ID NO.:37, SEQ ID NO.:38, SEQ ID NO.:14, SEQ ID NO.:16, SEQ ID NO.:18 or SEQ ID NO.:20; c) a light chain variable region which may comprise amino acids at least 90 consecutive amino acids of SEQ ID NO.:35 and a heavy chain variable region which may comprise at least 90 consecutive amino acids of any of SEQ ID NO.:36, SEQ ID NO.:37, SEQ ID NO.:38, SEQ ID NO.:14, SEQ ID NO.:16, SEQ ID NO.:18 or SEQ ID NO.:20; d) a light chain variable region which may comprise at least 90 consecutive amino acids of SEQ ID NO.:8 and a heavy chain variable region which may comprise at least 90 consecutive amino acids of any of SEQ ID NO.:36, SEQ ID NO.:37, SEQ ID NO.:38, SEQ ID NO.:14, SEQ ID NO.:16, SEQ ID NO.:18 or SEQ ID NO.:20; or e) a light chain variable region which may comprise at least 90 consecutive amino acids of SEQ ID NO.:10 and a heavy chain variable region which may comprise at least 90 consecutive amino acids of any of SEQ ID NO.:36, SEQ ID NO.:37, SEQ ID NO.:38, SEQ ID NO.:14, SEQ ID NO.:16, SEQ ID NO.:18 or SEQ ID NO.:20.

In accordance with a more specific embodiment of the invention, the light chain variable region may comprise at least 90 consecutive amino acids of SEQ ID NO.:8 or 10 and the heavy chain variable region may comprise at least 90 consecutive amino acids of SEQ ID NO.:14, 16, 18 or 20.
In accordance with an even more specific embodiment of the invention, the light chain variable region may be as set forth in SEQ ID NO.:8 or 10 and the heavy chain variable region may be as set forth in SEQ ID NO.:14, 16, 18 or 20.
More particularly, antibodies comprising the light chain variable region set fort in SEQ ID NO.: 8 and the heavy chain variable region set forth in SEQ ID NO.:14 are contemplated.
Other exemplary embodiments of the antibodies or antigen binding fragments of the invention are those which may comprise a light chain variable region which may comprise at least 90 consecutive amino acids of any of SEQ ID Nos. 39, 40, 41, or 24.
As used herein the term “at least 90 consecutive amino acids of SEQ ID NO.:39” also includes the terms “at least 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110 111 or at least 112, consecutive amino acids”. The term “at least 90 consecutive amino acids of SEQ ID NO.:39” encompasses any possible sequence of at least 90 consecutive amino acids found in SEQ ID NO.:39 and especially those sequences which include the 3 CDRs of SEQ ID NO.:39, for example a sequence comprising amino acids 6 to 102, 11 to 106, 1 to 106, 3 to 95, 5 to 95 of SEQ ID NO.:39 and so on.
As used herein the term “at least 90 consecutive amino acids of SEQ ID NO.:40” also includes the terms “at least 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111 or at least 112, consecutive amino acids”. The term “at least 90 consecutive amino acids of SEQ ID NO.:40” encompasses any possible sequence of at least 90 consecutive amino acids found in SEQ ID NO.:40 and especially those sequences which include the 3 CDRs of SEQ ID NO.:40, for example a sequence comprising amino acids 9 to 106, 10 to 101, 1 to 98, 3 to 99, 7 to 107 of SEQ ID NO.:40 and so on.
The terms “at least 90 consecutive amino acids of SEQ ID NO.:41” or “at least 90 consecutive amino acids of SEQ ID NO.:24” have similar meanings.
In accordance with the present invention, the antibody or antigen binding fragment of the present invention may have, for example, a light chain variable region as set forth in SEQ ID NO.:24.
The antibody or antigen binding fragment of the invention includes (or further includes) for example, a heavy chain variable region which may comprise at least 90 consecutive amino acids of any of SEQ ID NOs.:42, 43, 44 or 26.
As used herein the term “at least 90 consecutive amino acids of SEQ ID NO.:42” also includes the terms “at least 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117 or at least 118 consecutive amino acids”. The term “at least 90 consecutive amino acids of SEQ ID NO.:42” encompasses any possible sequence of at least 90 consecutive amino acids found in SEQ ID NO.:42 and especially those sequences which include the 3 CDRs of SEQ ID NO.:42, such as, for example a sequence comprising amino acids 6 to 111, 1 to 106, 2 to 104, 5 to 106, 10 to 107 of SEQ ID NO.:42 and so on.
As used herein the term “at least 90 consecutive amino acids of SEQ ID NO.:43” also includes the terms “at least 91, 92, 93, 94, 95, 96, 97, 98, 99, 100, 101, 102, 103, 104, 105, 106, 107, 108, 109, 110, 111, 112, 113, 114, 115, 116, 117 or at least 118 consecutive amino acids”. The term “at least 90 consecutive amino acids of SEQ ID NO.:43” encompasses any possible sequence of at least 90 consecutive amino acids found in SEQ ID NO.:43 and especially those sequences which include the 3 CDRs of SEQ ID NO.:43, such as, for example a sequence comprising amino acids 3 to 107, 1 to 115, 1 to 110, 22 to 116, 20 to 115 of SEQ ID NO.:43 and so on.
The terms “at least 90 consecutive amino acids of SEQ ID NO.:44” or “at least 90 consecutive amino acids of SEQ ID NO.:26” has a similar meaning.
In accordance with the present invention, the antibody or antigen binding fragment of the present invention may have, for example, a heavy chain variable region as set forth in SEQ ID NO.:26.
In accordance with the present invention the antibody or antigen binding fragment may comprise, for example,
a) a light chain variable region which may comprise at least 90 consecutive amino acids of SEQ ID NO.:39 and a heavy chain variable region which may comprise at least 90 consecutive amino acids of any of SEQ ID NO.:42, SEQ ID NO.:43, SEQ ID NO.:44 or SEQ ID NO.:26; b) a light chain variable region which may comprise at least 90 consecutive amino acids of SEQ ID NO.:40 and a heavy chain variable region which may comprise at least 90 consecutive amino acids of any of SEQ ID NO.:42, SEQ ID NO.:43, SEQ ID NO.:44 or SEQ ID NO.:26; c) a light chain variable region which may comprise amino acids at least 90 consecutive amino acids of SEQ ID NO.:41 and a heavy chain variable region which may comprise at least 90 consecutive amino acids of any of SEQ ID NO.:42, SEQ ID NO.:43, SEQ ID NO.:44 or SEQ ID NO.:26 or; d) a light chain variable region which may comprise at least 90 consecutive amino acids of SEQ ID NO.:24 and a heavy chain variable region which may comprise at least 90 consecutive amino acids of any of SEQ ID NO.:42, SEQ ID NO.:43, SEQ ID NO.:44 or SEQ ID NO.:26.

In accordance with a more specific embodiment of the invention, the light chain variable region may have at least 90 consecutive amino acids of SEQ ID NO.:24 and the heavy chain variable region may have at least 90 consecutive amino acids of SEQ ID NO.:26.
In accordance with an even more specific embodiment of the invention, the light chain variable region may be as set forth in SEQ ID NO.:24 and the heavy chain variable region may be as set forth in SEQ ID NO.:26.
Embodiments of the invention more particularly comprises an antibody or antigen binding fragment selected from the group consisting of:
a. an antibody comprising a light chain as set forth in SEQ ID NO.:7 and a heavy chain as set forth in SEQ ID NO.:13 or an antigen binding fragment thereof; b. an antibody comprising a light chain as set forth in SEQ ID NO.:7 and a heavy chain as set forth in SEQ ID NO.:15 or an antigen binding fragment thereof; c. an antibody comprising a light chain as set forth in SEQ ID NO.:7 and a heavy chain as set forth in SEQ ID NO.:17 or an antigen binding fragment thereof; d. an antibody comprising a light chain as set forth in SEQ ID NO.:7 and a heavy chain as set forth in SEQ ID NO.:19 or an antigen binding fragment thereof; e. an antibody comprising a light chain as set forth in SEQ ID NO.:7 and a heavy chain as set forth in SEQ ID NO.:29 or an antigen binding fragment thereof; f. an antibody comprising a light chain as set forth in SEQ ID NO.:7 and a heavy chain as set forth in SEQ ID NO.:59 or an antigen binding fragment thereof; g. an antibody comprising a light chain as set forth in SEQ ID NO.:7 and a heavy chain as set forth in SEQ ID NO.:60 or an antigen binding fragment thereof; h. an antibody comprising a light chain as set forth in SEQ ID NO.:7 and a heavy chain as set forth in SEQ ID NO.:61 or an antigen binding fragment thereof; i. an antibody comprising a light chain as set forth in SEQ ID NO.:9 and a heavy chain as set forth in SEQ ID NO.:13 or an antigen binding fragment thereof; j. an antibody comprising a light chain as set forth in SEQ ID NO.:9 and a heavy chain as set forth in SEQ ID NO.:15 or an antigen binding fragment thereof; k. an antibody comprising a light chain as set forth in SEQ ID NO.:9 and a heavy chain as set forth in SEQ ID NO.:17 or an antigen binding fragment thereof; l. an antibody comprising a light chain as set forth in SEQ ID NO.:9 and a heavy chain as set forth in SEQ ID NO.:19 or an antigen binding fragment thereof; m. an antibody comprising a light chain as set forth in SEQ ID NO.:9 and a heavy chain as set forth in SEQ ID NO.:29 or an antigen binding fragment thereof; n. an antibody comprising a light chain as set forth in SEQ ID NO.:9 and a heavy chain as set forth in SEQ ID NO.:59 or an antigen binding fragment thereof; o. an antibody comprising a light chain as set forth in SEQ ID NO.:9 and a heavy chain as set forth in SEQ ID NO.:60 or an antigen binding fragment thereof; p. an antibody comprising a light chain as set forth in SEQ ID NO.:9 and a heavy chain as set forth in SEQ ID NO.:61 or an antigen binding fragment thereof; q. an antibody comprising a light chain as set forth in SEQ ID NO.:23 and a heavy chain as set forth in SEQ ID NO.:27 or an antigen binding fragment thereof; r. an antibody comprising a light chain as set forth in SEQ ID NO.:23 and a heavy chain as set forth in SEQ ID NO.:46 or an antigen binding fragment thereof.

Other embodiments of the invention comprises an antibody or antigen binding fragment selected from the group consisting of:
a. an antibody comprising a light chain as set forth in SEQ ID NO.:5 and a heavy chain as set forth in SEQ ID NO.:13 or an antigen binding fragment thereof; b. an antibody comprising a light chain as set forth in SEQ ID NO.:5 and a heavy chain as set forth in SEQ ID NO.:15 or an antigen binding fragment thereof; c. an antibody comprising a light chain as set forth in SEQ ID NO.:5 and a heavy chain as set forth in SEQ ID NO.:17 or an antigen binding fragment thereof; d. an antibody comprising a light chain as set forth in SEQ ID NO.:5 and a heavy chain as set forth in SEQ ID NO.:19 or an antigen binding fragment thereof; e. an antibody comprising a light chain as set forth in SEQ ID NO.:5 and a heavy chain as set forth in SEQ ID NO.:29 or an antigen binding fragment thereof; f. an antibody comprising a light chain as set forth in SEQ ID NO.:5 and a heavy chain as set forth in SEQ ID NO.:59 or an antigen binding fragment thereof; g. an antibody comprising a light chain as set forth in SEQ ID NO.:5 and a heavy chain as set forth in SEQ ID NO.:60 or an antigen binding fragment thereof; h. an antibody comprising a light chain as set forth in SEQ ID NO.:5 and a heavy chain as set forth in SEQ ID NO.:61 or an antigen binding fragment thereof; i. an antibody comprising a light chain as set forth in SEQ ID NO.:7 and a heavy chain as set forth in SEQ ID NO.:11 or an antigen binding fragment thereof; j. an antibody comprising a light chain as set forth in SEQ ID NO.:7 and a heavy chain as set forth in SEQ ID NO.:30 or an antigen binding fragment thereof; k. an antibody comprising a light chain as set forth in SEQ ID NO.:9 and a heavy chain as set forth in SEQ ID NO.:11 or an antigen binding fragment thereof; and l. an antibody comprising a light chain as set forth in SEQ ID NO.:9 and a heavy chain as set forth in SEQ ID NO.:30 or an antigen binding fragment thereof.

The antibody or antigen binding fragment of the present invention may have a light chain variable region and/or heavy chain variable region as described above and may further comprise amino acids of a constant region, such as, for example, amino acids of a constant region of a human antibody.
In an exemplary embodiment, the antibody or antigen binding fragment of the present invention may comprise, for example, a human IgG1 constant region.
Anti-Siglec-15 antibodies of the IgG1 subtypes, which have, for example, an increase in activity of at least 10 fold in comparison with corresponding IgG2 subtypes *or other subtypes) are particularly contemplated.
An increase in the potency of the IgG1-based anti-Siglec-15 antibody of at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 95, 100 fold or more or an increase in its affinity of at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 20, 30, 40, 50, 60, 70, 80, 90, 95, 100 fold or more may be particularly useful.
The increased in potency or affinity may be measured by the ability of the IgG1-based anti-Siglec-15 antibody to inhibit osteoclast differentiation or osteoclast activity in comparison with a different antibody subtype having identical or substantially identical CDRs or variable regions. In some circumstances, it may be possible to consider using an IgG1 antibody concentration as low as 10 ng/ml or 100 ng/ml for attempting to inhibit osteoclast differentiation and/or bone resorption in vitro. It may be understood herein that lower dosage of IgG1-based anti-Siglec-15 antibodies may achieve a desired therapeutic effect when compared, for example, with a corresponding IgG2-based anti-Siglec-15.
Particularly contemplated antibodies include those having a kappa light chain constant region and an IgG1 heavy chain constant region.
Antibodies and antigen binding fragments of the invention include for example, monoclonal antibodies, polyclonal antibodies, human antibodies, humanized antibodies, chimeric antibodies having the amino acid sequence described herein. Human and humanized antibodies having the amino acid sequences identified herewith are particularly contemplated.
It is to be understood herein that the sequences of antibodies or antigen binding fragments thereof made of a) a light chain variable region set forth in SEQ ID NO.:6 and a heavy chain variable region set forth in SEQ ID NO.:12 or b) a light chain variable region set forth in SEQ ID NO.:22 and a heavy chain variable region set forth in SEQ ID NO.: 26 are considered of mouse origin (i.e., a non-human antibody).
As indicated herein, humanization of a non-human antibody may be performed for example, by substitution of framework amino acids for corresponding amino acids of a natural human antibody. Substitutions are usually made in a manner that does not negatively affect antigen binding.
In accordance with another exemplary embodiment of the invention, the antigen binding fragment may be, for example, a scFv, a Fab, a Fab′ or a (Fab′) 2 .
EXAMPLES
Based on binding assays to recombinant Siglec-15 and evaluation of their ability to inhibit the differentiation and activity of human osteoclasts, candidate lead antibodies 25D8 and 25E9 were selected for humanization. This experimental report describes the in silico humanization procedure and the resulting humanized versions of the antibodies.
Example 1
3D Modeling of the Variable Regions of the Mouse 25D8 and 25E9 Monoclonal Antibodies
This task was accomplished by homology modeling. The most similar template structures to the murine 25D8 (SEQ ID NO.:22 and SEQ ID NO.:26) and 25E9 (SEQ ID NO.:6 and SEQ ID NO.:12) variable sequences were identified by a blast searches against PDB. To build an initial model of the mouse 25D8 variable region the following template structures were used (PDB codes): 3CFC for the light chain, and 1NGQ for the heavy chain. To build an initial model of the mouse 25E9 variable region the following template structures were used: 1AE6 for the light chain, and 1NMC for the heavy chain. Mutations were operated on these template structures according to the murine 25D8 and 25E9 sequences: 3 mutations in 3CFC light chain (all in CDRs), 17 mutations in 1NGQ heavy chain (3 in the framework, 14 in CDRs), 7 mutations in 1AE6 light chain (4 in the framework, 3 in CDRs), and 34 mutations in 1NMC heavy chain (17 in the framework, 17 in CDRs). The CDR loops did not appear to require any adjustment in length except for the CDR-H3 loop in each antibody (2-residue deletion was made from 1NGQ to 25D8, and 1-residue insertion from 1NMC to 25E9). The mutated structures corresponding to the heavy and light chains of the murine 25D8 and 25E9 variable domains were virtually assembled into two-chain antibody structures by superimposing the heavy and light chains of the respective template structures. The resulting structures of assembled 25D8 and 25E9 variable domains were first refined by energy minimization with the AMBER force-field and a stepwise release of constraints, ranging from the CDR loops that were relaxed first, to the backbone heavy atoms of the framework region that were fully relaxed only in the last stage. The CDR-H3 loop in each antibody variable domain structure was then refined by Monte-Carlo-minimization (MCM) conformational sampling, in which dihedral angles in the CDR-H3 region were sampled in each MCM cycle followed by energy minimization of a predefined region extending 10 Å around the initial conformation of the CDR-H3 loop.
Representations of the modeled variable regions of the mouse 25D8 and 25E9 antibodies are given in FIGS. 1A and 1B , respectively. Homology 3D-models of the variable region of the mouse 25D8 ( FIG. 1A ) and mouse 25E9 ( FIG. 1B ) antibodies. CDRs are labeled (L1, L2, L3 in the light chain, and H1, H2, H3 in the heavy chain). Mouse framework residues replaced by human framework residues are indicated as blue sphere models. Retained mouse residues in the 25E9 heavy chain are represented by red sphere models and labeled.
The structures of the human or humanized variable sequences most similar to each of the 25D8 and 25E9 variable sequences were also identified from PDB, and then superimposed onto the modeled structures of the murine 25D8 and 25E9 variable domains. This assisted the modeling of side-chain mutations in the framework region in order to build the humanized 3D-structure starting from the modeled murine 3D-structures.
Example 2
Characterization of the Mouse 25D8 and 25E9 Amino-Acid Sequences and Modeled Structure
This step was carried out to estimate the humanness index, antigen contact propensity index, to delineate the CDRs, canonical residues, inter-chain packing (VHNL interface residues), variable-/constant-region packing (VH/CH and VL/CL interface residues), unusual framework residues, potential N- and O-glycosylation sites, buried residues, Vernier zone residues, and proximity to CDRs. Internet-available resources and local software were used to assess these properties.
Example 3
Selection of the Best Human Light-Chain and Heavy-Chain Frameworks for the Mouse CDRs
This was done by standard sequence homology comparison against a local copy of human germline databases (VBASE), against other sequence libraries (Genbank and SwissProt), as well as the set of human framework consensus sequences. BLAST searches were conducted to retrieve sequence matches with highest homology in the framework region only (thus excluding CDRs) while matching the length of the CDR loops. The human frameworks identified for the heavy and light chains correspond to the k2 and h1 classes, respectively, for both 25D8 and 25E9 antibodies. Several highly similar human framework sequences were retained in order to assess the amino-acid variability at candidate positions for mutation, as well as to provide a pool of suitable framework sequences as backup in the event of affinity loss upon humanization.
These homologous human framework sequences are aligned to the murine 25D8 and 25E9 sequences in FIGS. 2 and 3 , respectively. Kabat numbering and antigen contact propensity scores are shown at the top. CDRs are highlighted in grey. Candidate residues for back-mutations are highlighted below the sequence alignment according to proximity to CDRs, surface exposure, and contact with the pairing variable domain. Primary candidate positions for back-mutations are indicated by arrows.
Example 4
Identifying Mouse Framework Residues that can Influence Conformation and Antigen Binding
This is an important step that flags amino-acid residues that should be mutated to the corresponding human sequences with particular care. These residues represent primary candidates for back-mutations to the mouse sequences in case of affinity loss. It is the most difficult and unpredictable step of humanization by design, particularly in the absence of an experimental structure of the antibody-antigen complex. It relies on the identification of residues in one or more of the following categories: canonical, CDR-H3, Vernier zone, unusual, CDR-proximal (within 5 Å), inter-chain packing, and glycosylation-site residues. Such residues might affect antigen-binding site and affinity directly or indirectly. The antigen contact propensity index as well as amino-acid occurrence in human germline databases at each position are also extremely important in deciding whether a certain residue can be safely mutated from the mouse sequence to the human sequence. The proposed humanized sequences of the 25D8 and 25E9 light and heavy variable sequences are shown in FIGS. 2 and 3 , respectively. The number of framework mutations between each humanized sequence and their donor mouse sequence and several aligned candidate acceptor human sequences are also listed (given as percentage of the framework in parentheses). Mutated residues and candidate residues for back-mutations are also indicated in FIGS. 1, 2 and 3 . As it can be seen, the light chains of the 25D8 and 25E9 antibodies appear to require 9 and 11 mutations to their respective proposed humanized framework, respectively. This represents a 100% framework humanization attempt for the light chains. The heavy chain of each antibody appears to require substantially more mutations than their light chains for humanization, 18 in the case of 25D8 and 17 in the case of 25E9. In addition, the humanized sequences for the heavy chains do not correspond fully (100%) to human framework sequences. Particularly in the case of the 25E9 heavy chain, the highest level of framework humanization proposed is 94% in a first attempt, which translates into 5 residues differing in the humanized sequence from the closest human framework sequence. The decision to retain 4 of these residues from the 25E9 mouse sequence was based on careful structural and comparative sequence analyses that indicated a high probability of altering antigen-binding affinity if mutations are to be introduced at these positions: GluH1, IleH2, ThrH93, and SerH94 due to proximity to antigen-binding CDRs (see FIG. 1 b ). It must be noted that Glu is a common residue found at the H1 position in human framework sequences (see FIG. 3 ). A fifth residue differing in the humanized sequence from the closest human framework is His H43 in the mouse sequence, that was mutated to GlnH43 in the humanized sequence (Gln is common at this position while His is rare). In the case of humanization of the 25D8 variable heavy chain framework, that reached 99%, i.e., one residue difference in the framework of the proposed humanized sequence relative to the closest human framework sequence: GluH81 in the humanized sequences replaced GlnH81 of the mouse sequence instead of AspH81 that appears in the closest human framework. The decision to mutate to Glu instead of Asp at position H81 was based on the relative occurrence of these two possible substitutions in human frameworks (see FIG. 2 ). Overall, it can be concluded that humanization of the 25D8 antibody is easier than that of the 25E9 antibody.
Example 5
Additional Structural Analysis
Prior to submitting the humanized sequence for recombinant expression, additional structural analysis included selection of signal peptide, selection of isotype, and analysis of structural compatibility at the variable-/constant-region junctions. In addition, a comparative analysis of inter-chain packing and variable-/constant-region packing between mouse and humanized antibodies indicated that in the case of 25D8 and 25E9 humanizations it may be feasible to generate hybrid antibodies combining humanized and chimeric (mouse variable region) chains, i.e., mouse/mouse (M/M), mouse/humanized (M/H), humanized/mouse (H/M) and humanized/humanized (H/H) as light-chain/heavy-chain pairing. Assembled humanized and chimeric sequences for the 25D8 and 25E9 full-length IgG 2 antibodies are shown in FIGS. 4A and 4B , respectively. Assembled humanized and chimeric sequences for the 25D8 and 25E9 full-length IgG1 antibodies are shown in FIGS. 12A and 12B , respectively.
Other exemplary embodiments of antibodies may be generated, for example, by mixing each of the light chains disclosed herein with each of the heavy chain variants disclosed herein. For example, antibodies may be generated by the association of a light chain and heavy chain comprising respectively the 25E9 light chain humanized variant 2 variable domain (SEQ ID NO.:10) and the 25E9 heavy chain humanized variable domain variants 1, 2, 3 or 4 (SEQ ID NO.:14, 16, 18 or 20). Antibodies generated by the association of a light chain and heavy chain comprising respectively, the 25E9 light chain humanized variant 1 variable domain (SEQ ID NO.:8) and the 25E9 heavy chain humanized variable domain variants 1, 2, 3 or 4 (SEQ ID NO.:14, 16, 18 or 20) are particularly contemplated. Humanized 25E9 antibodies comprising the light chain humanized variant 1 variable domain (SEQ ID NO.:8) and the heavy chain humanized variable domain variant 1 (SEQ ID NO.:14) (a.k.a., the L1H1 IgG2 variant (SEQ ID NOs.:7 and 29) or the L1H1 IgG1 variant (SEQ ID NOs.:7 and 13)) have been selected for further experimentation. However, based on experiments disclosed herewith, it appears that antibodies having a kappa light chain constant region and an IgG1 heavy chain constant region have interesting characteristics (e.g., L1H1 IgG1 variant (SEQ ID NOs. 7 and 13)).
Antibodies or antigen binding fragments made by the association of the light chain of SEQ ID NO.:7 with any of the heavy chains set forth in SEQ ID NOs. 13, 15, 17, 19, 29, 59, 60 or 61 or by the association of the light chain of SEQ ID NO.:9 with any of the heavy chains set forth in SEQ ID NOs. 13, 15, 17, 19, 29, 59, 60, or 61 are contemplated.
Example 6
Analysis of the Binding Parameters of Humanized Siglec-15 Antibodies
Small lots of the mouse and selected humanized or chimeric 25D8 IgG2 and humanized 25E9 (the L1H1 IgG2, L1H1 IgG1, L1H2 IgG1, L1H3 IgG and L1H1 IgG1 variants) antibodies were produced by transient transfection and purified to allow some comparative analyses to be conducted. A Surface Plasmon Resonance (SPR) method was used to measure the direct binding of recombinant Siglec-15 with the different antibodies. As with the ELISA methods, Siglec-15 that was used in the SPR experiments was expressed as a Fc-Siglec-15 fusion protein in 293-6E cells. It should be noted that as a Fc conjugate, the protein may be expressed as dimer by virtue of the homodimeric interaction in the Fc region. This occurrence could produce avidity effects during the binding that did not allow a direct determination of affinity constants. In addition, the presence of the Fc region in both the antibodies and the Siglec-15 protein does not permit direct affinity determinations. Thus, the binding results of each antibody sample are presented only in relation to each other.
To conduct the study, the heavy and light immunoglobulin chains from either chimeric (mouse variable regions) 25D8 IgG2, chimeric 25E9 IgG2, humanized 25D8 IgG2 or the humanized 25E9 L1H1 IgG2 variant were used directly. For comparison, purified preparations of full mouse antibodies were also tested. In the case of the purified batches of antibodies, size-exclusion chromatography was applied to all protein samples to reduce the proportion of aggregates in the preparations. For SPR, the Fc-Siglec-15 was immobilized on the sensor chip and antibody dilutions were injected (flowed) over the chips. Representative scans for the 25D8 and the 25E9 antibodies are shown in FIGS. 5A and 5B , respectively.
For the 25D8 antibody, the scans were very similar between the mouse, chimeric and humanized versions of the antibody. This showed that the kinetic parameters were not significantly altered during the humanization of this antibody. Although there are slight differences between the chromatograms, this was to be expected given the fact that the comparison was conducted between purified antibodies and cell supernatants.
In the case of the 25E9 antibody, the chromatograms for the chimeric and mouse antibodies were very similar. For the humanized 25E9 L1H1 IgG2 variant, the on and off rates appeared to be slightly different compared to the other versions. This was likely due to interference from the cell supernatants. Despite this difference, the actual affinity constant of the humanized 25E9 L1H1 IgG2 variant was expected to be very similar to that of the mouse antibody.
We tested the ability of the humanized antibodies to interact with human Siglec-15 expressed on the surface of cultured cells. Human 293-6E cells were grown to a cell density of approximately 1.5×10 6 cells/ml and transfected with an expression plasmid that encodes the entire human Siglec-15 cDNA. Twenty-four hours later, the cells were harvested, counted and 1×10 5 cells were incubated with increasing concentrations of the humanized IgG1 variant of 25E9 for 1 hour at 4 C. Following a washing step with cold PBS, bound 25E9 was detected with an anti-human kappa light chain IgG conjugated to FITC. Fluorescently labeled cells were injected into a flow cytometer to measure the fluorescence signal on the surface of intact cells. As shown in FIG. 8 , the humanized 25E9 L1H1 IgG1 variant binds to cells expressing human Siglec-15 in a concentration dependent manner. The average K D was in the low nanomolar range. Furthermore, the binding parameters were very similar in the presence of the humanized 25E9 L1H1 IgG1 variant produced in either CHO cells or 293 cells. As a control, transfected cells incubated with either PBS, a control IgG or untransfected 293 cells resulted in no fluorescence signal indicating the specificity of the interaction between Siglec-15 and the humanized 25E9 L1H1 IgG1 variant. Similar results were obtained with other 25E9 humanized IgG1 antibody variants (the L1H2 IgG1, the L1H3 IgG1, the L1H4 IgG1 and, the L1H1 IgG2) or with the humanized 25D8 IgG2 antibody.
Example 7
Antibody Testing
Cell Culture
To induce osteoclast differentiation, mouse RAW264.7 cells (ATCC, Manassas, Va.), grown in DMEM containing 10% fetal calf serum (Gibco) and 1 mM sodium pyruvate, were scraped and resuspended in PBS. Cells were plated at 2×10 4 cells/cm 2 in media containing 100 ng/ml mouse RANKL (R&D Systems, Minneapolis, Minn.). Cells were allowed to differentiate for 3 days (for immunofluorescence microscopy) or 4 days (for all other experiments). Human osteoclast precursors (CD14+ peripheral blood mononuclear cells (PBMCs)) were isolated from normal human PBMCs (AllCells, Emeryville, Calif.) using CD14 microbeads and MS columns (Miltenyi Biotec, Cologne, Germany) following the manufacturer's instructions. Cells were plated at 3.1×10 5 cells/cm 2 in Alpha-MEM (Gibco) containing 10% fetal calf serum (HyClone), 1 mM sodium pyruvate (HyClone), 25 ng/ml human MCSF and 30 ng/ml human RANKL (R&D Systems). Cells were allowed to differentiate for 7 days, with half of the media replaced on Day 4.
Cell Stimulation
For cell stimulation with single antibodies, differentiation media was replaced with fresh growth media (without RANKL) containing the indicated antibody concentrations before lysing the cells at various times. For stimulations with primary and secondary (crosslinking) antibodies, differentiation media was replaced with cold growth media containing the primary antibody at 10 ug/ml, and cells were incubated 20 min at 4 C. Media was then replaced with warm growth media containing goat anti-human IgG polyclonal antibody (Jackson Immunoresearch, West Grove, Pa.) and cells were incubated for the indicated times at 37 C before lysis.
Osteoclast TRAP Staining and In Vitro Functional Assays
To test the effect of antibodies on osteoclast differentiation and function, cells were induced to differentiate, as described above, in media containing indicated concentrations of antibodies. Osteoclasts were visualized after four days in culture by TRAP staining: briefly, cells were fixed in 3.7% formaldehyde, permeabilized with 0.2% Triton X-100/PBS, and incubated in TRAP staining buffer (100 mM sodium acetate, pH 5.2, 50 mM sodium tartrate, 0.01% Naphthol ASMX and 0.06% Fast Red Violet) for approximately 30 min at 37 C. The TRAP enzyme generates a red reaction product in osteoclasts. To test osteoclast resorption activity, cells were seeded in wells coated with a calcium phosphate substrate (Osteologic, BD BioSciences or OsteoAssay, Corning) and induced to differentiate as above. After 7 days, wells were treated with bleach to remove cells, and areas of substrate resportion were observed by light microscopy. Antibodies that are able to block the activity of Siglec-15 (in osteoclast or in osteoclast precursor cells) may show, for example, fewer TRAP-positive multinucleated cells or may result in an altered morphology of the TRAP-positive multinucleated cells. This is illustrated in FIG. 9 . As shown in the upper panels, human osteoclasts exposed to 1 μg/ml of the humanized 25E9 antibody (the L1H1 IgG1 variant) (upper right panel) were unable to properly form mature multinucleated osteoclasts. By contrast, human osteoclasts treated with an equal quantity of a control antibody differentiated normally (upper middle panel). As osteoclasts actively digest mineralized substrate, antibodies that are able to block the activity of Siglec-15 (in osteoclast or in osteoclast precursor cells) may show, for example, fewer areas where the calcium substrate has been digested (denuded area) in comparison with a control (e.g., antibodies that do not bind to Siglec-15, absence of antibodies etc.). When the human osteoclasts were differentiated on a calcium phosphate substrate (see FIG. 9 ), which acts as a bone-like surface, cells treated with the control antibody (lower middle panel) generated large areas of denuded calcium phosphate indicating that the osteoclasts exhibited resorptive activity. By contrast, cells treated with 1 μg/ml 25E9 (the L1H1 IgG1 variant) (lower right panel) were unable to resorb the substrate, which was comparable to the undifferentiated precursor cells (lower left panel).
The ability of the 25D8 antibody to inhibit osteoclasts was also preserved after humanization, although its potency always remained lower than that of the 25E9 antibodies (whether humanized or chimeric 25E9).
Another technique involves CD14+ PBMCs that are differentiated into osteoclasts and plated on bovine cortical bone slices (differentiation may be done before plating, upon plating or after plating). The anti-Siglec-15 is added and resorption pits generated on the bone slice surface are observed by reflected light microscopy. Antibodies that are able to block the activity of Siglec-15 (in osteoclast or in osteoclast precursor cells) may result, for example, in fewer or smaller resorption pits.
Our results indicate that anti-Siglec-15 humanized antibodies are able to inhibit osteoclast differentiation and/or bone resorption.
Internalization Assay
To biotinylate cell-surface proteins, differentiated RAW264.7-derived osteoclasts were rinsed twice with cold PBS containing 1 mM CaCl 2 and 1 mM MgCl 2 (PBS/Ca/Mg, HyClone) and incubated with the biotinylation reagent sulfo-NHS-SS-biotin (Pierce), diluted to 1 mg/ml in PBS/Ca/Mg for 1 h at 4 C. The reaction was stopped by quenching unreacted biotinylation reagent with glycine (100 mM in PBS/Ca/Mg). To induce Siglec-15 internalization, cells were treated with anti-Siglec-15 antibody or a control human IgG alone or in combination with a secondary crosslinking antibody, as described in “Cell stimulations”, above. Following antibody treatments, cells were rinsed twice with cold NT buffer (20 mM Tris/HCl, pH 8.6, 150 mM NaCl, 1 mM EDTA and 0.2% BSA) and incubated 2×25 min with sodium-2-mercaptoethane sulfonate (MesNa), prepared at 25 mM in cold NT buffer, to reduce the disulfide bond of sulfo-NHS-SS-biotin and thereby remove any remaining cell-surface biotin. To gauge the maximum possible level of Siglec-15 biotinylation, this MesNa treatment was omitted for one control (these control cells were incubated 2×25 min with NT buffer alone). The remaining MesNa was then quenched with iodoacetamide, diluted to 5 mg/ml in PBS/Ca/Mg, for 15 min.
To evaluate the amount of biotinylated Siglec-15 that had been internalized by the osteoclasts, cells were lysed in mRIPA. Biotinylated proteins were collected by streptavidin pull-down: 250 μg of lysate was incubated overnight with 50 μl of Dynal MyOne streptavidin beads (Invitrogen), rotating at 4 C. After extensive washing, Siglec-15 was detected in the precipitated material by western blotting.
Siglec-15 is Internalized and Degraded Following Antibody Ligation
The ability to mediate endocytosis of bound ligands and antibodies has been demonstrated for some members of the Siglec family; indeed, the cellular uptake of therapeutic antibodies is a critical aspect of the mechanism of action of antibody-drug conjugates targeting the CD22 and CD33 Siglecs (O'Reilly and Paulson, 2009). Interestingly, Siglec-15 also contains a Yxxφ sequence in its cytoplasmic domain (this tyrosine, Y309, is also part of a putative ITIM motif); Yxxf motifs can interact with the clathrin adapter AP-2 to regulate receptor internalization (Angata et al., 2007; Bonifacino and Traub, 2003). Thus, we investigated the effect of antibody ligation on Siglec-15 endocytosis in osteoclasts.
We first tested whether a Siglec-15 antibody, either alone or in combination with a secondary crosslinking antibody, could induce internalization of Siglec-15, labeled with biotin, from the surface of RAW264.7-derived osteoclasts. After the antibody stimulation, any remaining cell-surface biotin was released by treatment with a reducing agent. Cells were then lysed, and internalized, and biotinylated proteins were collected with streptavidin beads. Siglec-15 was detected in the precipitated material by western blotting. Interestingly, we found that treatment with Siglec-15 antibody alone induced substantial internalization compared to a control human IgG ( FIG. 10A , compare lances 7 and 8), while addition of a secondary antibody to induce receptor clustering had less of an effect than the single antibody ( FIG. 10A , lane 5).
We proceeded to characterize the antibody-induced endocytosis of Siglec-15 by immunofluorescence microscopy. RAW264.7-derived osteoclasts, growing on glass coverslips, were “cold-loaded” with anti-Siglec-15 diluted in normal growth media at 4 C, conditions that should permit antibody binding but not endocytosis. Cells were then fixed immediately or incubated in antibody-free warm media for different times prior to fixation. As expected based on the distribution of Siglec-15 in fixed, permeabilized osteoclasts, in intact osteoclasts, cold-loaded Siglec-15 antibodies bound strongly at the cell surface. After a 10-min incubation at 37 C, the staining pattern was clearly altered: Siglec-15 antibodies were present in internal punctae that are likely endosomes ( FIG. 10B , center panel). While after 10 min the Siglec-15 signal was still near the plasma membrane, after 45-min it became mostly perinuclear, which is a typical lysosomal staining pattern (Toyomura et al., 2003). This was confirmed by co-staining these cells for the lysosome marker LAMP-2. Indeed, at 45 min there was substantial co-localization of Siglec-15 and LAMP-2 in perinuclear regions, whereas at earlier time points, the staining patterns were clearly divergent ( FIG. 10B ).
Lysosomes are principal sites of receptor degradation following endocytosis. To determine whether this is the fate of Siglec-15, we treated RAW264.7-derived osteoclasts with antibodies over a prolonged time course and analyzed total protein extracts by western blotting. Our results indicate that there was a clear decrease in Siglec-15 protein levels beginning within 3 h of addition of anti-Siglec-15 ( FIG. 10C , lanes 4 and 6). In contrast, exposure of the osteoclasts with a control IgG did not cause this reduction in signal. Notably, a similar reduction in Siglec-15 protein levels was detected in RAW264.7 cells differentiated with RANKL (for 4 d) in the presence of anti-Siglec-15 ( FIG. 10D ). Together, these results demonstrated that bivalent anti-Siglec-15 antibodies induce rapid internalization of the receptor, which is then targeted to lysosomes for degradation.
Example 8
Preparation of Cell Lysates and Immunoprecipitation
Cell lysates were prepared using mRIPA lysis buffer (50 mM Tris/HCl pH 7.4, 1% NP-40, 0.25% deoxycholate, 150 mM NaCl) containing protease and phosphatase inhibitors (50 mM NaF, 1 mM NaVO 4 and 1× Roche Complete EDTA-free phosphatase inhibitors). Lysate protein concentrations were measured by BCA assay (Pierce). For western blotting of total cell lysates, equal amounts of protein (10-15 ug) were heat-denatured in SDS sample buffer containing β-mercaptoethanol, separated on a 10 or 12% SDS-PAGE gel, transferred to PVDF and probed with the indicated antibodies. For immunoprecipitations, 2 mg or 1 mg of total lysates were incubated with 4 μg antibody and 15 μl of Protein G-Sepharose beads for 4 h, rotating at 4 C. After washing the beads 4× with mRIPA, half of the precipitated material was analyzed by western blotting, as above.
Interaction Between Siglec-15 and DAP12 and Multimerization of Siglec-15
A recent study demonstrated that upon co-overexpression of epitope-tagged forms of Siglec-15 and DAP12 in 293T cells, a complex could be detected, which was dependent on the presence of K273 (Angata et al., 2007). We were also able to detect this complex under similar overexpression conditions (data not shown), and we proceeded to determine whether the complex is also present at endogenous expression levels in osteoclasts. Protein lysates were prepared from differentiated RAW264.7-derived osteoclasts as well as from non-differentiated control cells, and immunoprecipitations were performed using Siglec-15 and DAP12 antibodies. DAP12 was readily detected in protein complexes precipitated with anti-Siglec-15, and likewise, anti-DAP12 precipitated abundant Siglec-15. As expected, based on Siglec-15 protein expression levels, this complex was highly osteoclast-specific and was not detected in non-differentiated cells. Notably, DAP12 expression was not dramatically altered during RAW264.7 osteoclast differentiation.
Previous studies showed that when phosphorylated on its ITAM motif, DAP12 is capable of activating a number of signaling pathways, including the PI3K-Akt, PLCg and Grb2-Ras-Erk cascades (Turnbull and Colonna, 2007). However, the signaling output of DAP12 in specific contexts is highly dependent on its associated receptor (Turnbull and Colonna, 2007). In the absence of an identified natural ligand or molecular partner for Siglec-15, we used an antibody cross-linking approach to evaluate the ability of Siglec-15 to activate intracellular signaling. Initially, we treated RAW-derived osteoclasts with anti-Siglec-15 for multiple time points up to 30 min but failed to observe any activation of Akt, PLCg, or Erk (data not shown). However, for several other DAP12-associated receptors, higher-order clustering of the receptor, rather than bivalent antibody-induced dimerization, is required to induce ITAM-dependent signaling (Turnbull and Colonna, 2007; Underhill and Goodridge, 2007). To induce multimerization, we treated cells with a primary Siglec-15 antibody followed by a secondary, crosslinking antibody. Under these conditions, we observed a signaling effect ( FIG. 11 , lanes 5, 8 and 11), with Akt becoming strongly phosphorylated within minutes of secondary antibody crosslinking. Maximum phosphorylation of Akt was achieved after 5 min of treatment with anti-Siglec-15 ( FIG. 11 , lane 8). In contrast, phospho-Erk ( FIG. 11 ) and phospho-PLCg (not shown) were not modulated. Consistent with the lack of expression of Siglec-15, there was no activation of Akt in non-differentiated RAW264.7 cells under the same conditions. Likewise, substitution of the primary Siglec-15 antibody with a control human IgG eliminated the signaling response ( FIG. 11 , see lanes 3, 6, 9 and 12). These results demonstrated that Siglec-15 crosslinking specifically activates Akt without affecting Erk or PLCg, two other pathways commonly downstream of DAP12 (Turnbull and Colonna, 2007; Underhill and Goodridge, 2007).
If induction of cell signaling by Siglec-15 is dependent on the DAP12 ITAM motif, tyrosine phosphorylation of DAP12 should be detectable upon Siglec-15 clustering. To test this, we immunoprecipitated DAP12 and evaluated its phosphorylation by western blotting. In RAW264.7-derived osteoclasts stimulated with primary/secondary antibodies to crosslink Siglec-15 (as described above), we detected a tyrosine-phosphorylated band at 12 kDa that is very likely DAP12. In non-differentiated cells treated in the same manner or osteoclasts treated with a control human IgG, little or no DAP12 phosphorylation was detected. Notably, although abundant Siglec-15 was co-precipitated with DAP12 from the differentiated osteoclasts (as expected), no phosphotyrosine signal was detected at its molecular weight (37 kDa), indicating that phosphorylation of the cytoplasmic tyrosine residue of Siglec-15, part of its putative ITIM motif, is not involved in the signaling response (data not shown). Thus, our results are consistent with DAP12 acting as a signaling module for Siglec-15; DAP12 becomes phosphorylated following Siglec-15 clustering, likely leading to recruitment of signaling molecules to its ITAM motif and activation of the Akt pathway.
Anti-Siglec-15 antibodies capable of inhibiting dimerization or multimerization of Siglec-15 may thus inhibit Siglec-15 activity in osteoclasts or in osteoclast precursors. For example, in order to determine the ability of an antibody to inhibit dimerization or multimerization of Siglec-15, the level of activation of DAP12 (e.g., DAP12 phosphorylation) and/or of its downstream effectors (Akt pathway) may be tested.
Example 9
Comparison of IgG1 and IgG2 Antibody Variants
We proceeded to compare humanized anti-Siglec-15 IgG1 antibody variants with corresponding humanized anti-Siglec-15 IgG2 antibody variants (i.e., the antibodies have the same variable domains but the human constant region of the heavy chain differs) and found that, in the in vitro experiments described below, IgG1s are much more active than the corresponding IgG2s.
More particularly, we compared the binding activity of the humanized 25E9 L1H1 IgG1 (the L1H1 IgG1 variant) with the humanized 25E9 L1H1 IgG2 (the L1H1 IgG2 variant) using SPR. The analysis was conducted using methods similar to what was described above (see Example 6). In this instance, Fc-Siglec-15 was immobilized on the chip and decreasing concentrations of the 25E9 antibody variants were injected (100 nM, 33.3 nM, 11.1 nM, 3.70 nM and 1.23 nM). The result showed that the affinity of the humanized 25E9 L1H1 IgG1 variant for Siglec-15 was almost 10-fold higher than the humanized 25E9 L1H1 IgG2 variant with comparative KD values of 0.164 nM and 1.26 nM, respectively (see FIG. 12 ). The difference in binding was mostly contributed by a slower off-rate (kd) of the IgG1 compared to the IgG2.
The ability to inhibit human osteoclast differentiation of the humanized 25E9 L1H1 IgG1 variant (the L1H1 IgG1 variant) and IgG2 (the L1H1 IgG2 variant) was also examined. Human osteoclast precursor cells were enriched and differentiated as described above in the presence of increasing concentrations of the antibodies (see FIG. 13 ). In the presence of the humanized 25E9 L1H1 IgG1 variant, less than 100 ng/ml of antibody is required to completely inhibit the differentiation of osteoclasts in this assay. By contrast, 10 μg/ml of the humanized 25E9 L1H1 IgG2 variant is required to obtain the same degree of inhibition. This represents an almost 100-fold difference in potency of the humanized 25E9 L1H1 IgG1 variant versus the corresponding IgG2 variant. In control samples, the differentiation of osteoclasts exposed to either the vehicle or a control IgG at 10 μg/ml was unaffected. Although the increase in potency of IgG1-based antibodies was demonstrated for the L1H1 variant, such increase is also expected for the other 25E9 humanized variants, hybrid or mouse antibodies.
In fact, we also observed that the potency of another Siglec-15 humanized antibody, 25D8, was highly augmented as an IgG1 versus and IgG2. It is expected that other anti-Siglec-15 antibodies may benefit from having a human IgG1 constant region instead of other types of constant region. Such antibodies may be identified by measuring an increase in affinity of the IgG1-based anti-Siglec-15 antibody towards cells expressing Siglec-15 or towards recombinant Siglec-15, or testing the ability of the IgG1-based antibody to inhibit osteoclast differentiation or activity (in vitro or in vivo).
Based on these results, human IgG1-based anti-Siglec-15 antibodies may advantageously be administered at lower dosage in human.
Example 10
Antibody-Drug Conjugates (ADC) that Target Siglec-15
The Applicant demonstrated that binding of an antibody to Siglec-15 expressed on the surface of osteoclasts was efficiently internalized and degraded. Additional studies also indicated that the internalization followed the endosomal pathway and the Siglec-15/antibody complex could be co-localized with LAMP2, a marker of late-endosomes/lysosomes. Experiments were undertaken to examine the feasibility of targeting Siglec-15-expressing cells with an ADC. The humanized 25E9 L1H1 IgG1 variant was conjugated to a payload that is toxic to proliferating cells as well as non-proliferating or fully differentiated cells, in particular osteoclasts. The humanized 25E9 L1H1 IgG1 conjugated antibody was designated 25E9-ADC. Since the conjugation might affect the ability of 25E9 to interact with native Siglec-15, flow cytometry was conducted to measure the binding of the 25E9-ADC to Siglec-15 expressing cells. The experiments were performed as described above using 293-6E cells transfected with a cDNA encoding the human Siglec-15. As illustrated in FIG. 15 , unconjugated 25E9 and the 25E9-ADC interacted with the Siglec-15-transfected cells with very similar affinities (see black curves, h-Siglec-15). This indicated that the conjugation reaction did not alter the ability of the 25E9-ADC to bind to Siglec-15. As a control, cells transfected with the plasmid not containing the Siglec-15 cDNA (see FIG. 15 grey curves, vector) did not bind to 25E9 indicating that the antibodies do not bind to the cells non-specifically.
The cytotoxic activity of the antibodies was examined next. Human osteoclast precursor cells were isolated and seeded in 96-well plates in the presence of M-SCF and RANKL, in a manner similar to what was described previously. The osteoclasts were allowed to differentiate for 7 days in order to become fully mature, multi-nucleated TRAP-positive osteoclasts. Following differentiation, the cells were treated with unconjugated 25E9, 25E9-ADC or the control-ADC for 4 days. The remaining cell number (% survival) was determined using standard calorimetric methods. As expected, unconjugated 25E9 had no effect on the survival of human osteoclasts (see FIG. 16 ). This result was in agreement with previous results showing that despite potent inhibition of osteoclast differentiation by 25E9, the antibody does not kill the cells. By contrast, the 25E9-ADC showed dose-dependent decrease in the number of surviving cells ( FIG. 16 ), a result consistent with cytotoxicity of the delivered toxin. The IC 50 value of this cytotoxicity was in the sub-nanomolar range. The control ADC, which does not bind to human Siglec-15, showed mild non-specific activity in this assay. At the end of the study, the cells were fixed and stained for TRAP activity using methods that were described in Example 7 in order to visually inspect the effect of the antibodies on the osteoclasts. As shown in FIG. 17 , treatment with unconjugated 25E9 (upper panels) had a severe effect on the morphology of the osteoclasts resulting in small, intensely-TRAP stained cells, which we have previously shown are non-functional and completely devoid of resorptive activity (see FIG. 9 ). Treatment with the 25E9-ADC resulted in death of the osteoclasts and virtually all of the cells were gone at 1 μg/ml (see FIG. 17 , middle panels), a result that was in agreement with the cell number determinations shown in FIG. 16 . Finally, the control-ADC did not show any toxic effects on the mature osteoclasts (see FIG. 17 , lower panels) and the number of osteoclasts, even at 10 μg/ml, was similar to the number observed with the untreated cells. These results indicate that the cytotoxicity observed with the 25E9-ADC was specific to Siglec-15-positive osteoclasts.
Taken together, these results show that ADCs that target Siglec-15 expressed on the surface of osteoclasts have cytotoxic activity.
Example 11
In Vivo Functional Assay—Mouse
Evaluation of in vivo efficacy was adapted from the methods described by Schenk (Muhlbauer et al., 1991) using very young mice that have rapidly growing bones. Briefly, 3-4 week-old male mice (5 animals/group) were treated with either, PBS, a control mouse IgG or an anti-Siglec-15 antibody capable of binding to mouse Siglec-15. The antibodies were administered intra-peritoneally twice per week for four weeks using 26G needles. The mice were sacrificed, and bones were dissected and fixed in 4% paraformaldehyde for 24 h. After washing in PBS, the bones were scanned using a PIXImus Densitometer (GE Medical Systems) to determine the bone mineral density (BMD) of the femurs, the tibias and the vertebrae. Three-dimensional images of the bones were generated with a SkyScan high resolution microCT (SkyScan Inc., Kontich, Belgium).
For these experiments, 3-4 week old mice were treated with an anti-Siglec-15 antibody for four weeks and assessed the effects of this treatment on the long bones and the vertebrae. Since young mice have rapidly growing bones at this age, the perturbation of osteoclast activity by anti-resorptives can provoke a rapid, dramatic increase in bone mineral density (BMD) in a relatively short period of time. Following the treatment period, the animals were euthanized, the bones were dissected and scanned by densitometry to calculate the BMD. Compared to a control mouse IgG, treatment with the anti-Siglec-15 monoclonal antibody resulted in a considerable, dose-dependent increase in BMD in the femur, tibia and vertebra of these mice. In order to further examine the changes in BMD, selected bone samples were scanned using X-ray microtomography (MicroCT) to analyze their microarchitecture. In agreement with the densitometry result, we observed a marked increase in trabecular volume in the femurs and the vertebra of the mice treated with the anti-Siglec-15 antibody compared with the control IgG-treated mice and the L5 vertebra. In agreement with these qualitative observations, quantitative measurements of the microCT scans confirmed the increase in bone mineral density in the animals treated with the Siglec-15 antibody. In particular, there were statistically significant increases in bone volume, bone surface, trabecular number and connectivity density. Conversely, the trabecular separation was significantly decreased, a change that was in line with the increased density of trabecular structures.
The objective of the following study was to determine the effect of an antibody targeting Siglec-15 in the rat ovariectomy (OVX) model.
Thirty-two Sprague-Dawley rats were sham operated or ovariectomized and treated 12 weeks later with PBS (q28d), Siglec-15 antibody (an anti-mouse Siglec-15 antibody, 10 mg/kg, q28d) or zoledronic acid (ZOL, 0.1 mg/kg, single injection). After a twelve-week treatment, bones were analyzed by densitometry, microCT, histomorphometry, 3-point bending (femur) and axial compression (LV4) and serum was analyzed for TRAP 5b and ALP levels.
As expected, bone mineral density (BMD) was reduced dramatically in the OVX-PBS group compared to the sham operated animals, while ZOL treatment increased BMD. Administration of 25B2 caused a significant increase in BMD at all sites. These changes were confirmed by microCT analyses, which showed significant increases in bone volume, trabecular (Tb) number and corresponding decreases in Tb separation compared to control group. Correspondingly, improvements in bone strength in animals treated with the anti-mouse Siglec-15 antibody were observed by biomechanical analysis: maximum load, stiffness and energy-to-failure parameters were all increased. Examination of tibial sections showed that the number of osteoclasts was significantly increased by the anti-mouse Siglec-15 antibody treatment, but the TRAP-positive cells were smaller and more intensely stained. Serum TRAP 5b was decreased in the anti-mouse Siglec-15 antibody group consistent with a decrease in secretion of this enzyme by osteoclasts. Interestingly, the serum level and the histological staining of ALP were unchanged in the antibody-treated animals. This contrasts with the effect of ZOL treatment, which caused a significant decrease in ALP staining. Dynamic histomorphometry analysis using dual-calcein labeling indicated that the endosteal mineral apposition rate was greater in the antibody-treated group compared to both the vehicle and ZOL treated groups, suggesting stimulation of new bone formation by the anti-Siglec-15 antibody.
Taken together, our results reveal that targeting Siglec-15 with a monoclonal antibody in a pathologic bone loss model improves bone quality and strength, likely due to combined inhibition of osteoclast function and maintenance of osteoblast activity.
In Vivo Functional Assay—Monkeys
To explore the effects of Siglec-15 inhibition on bone biomarkers in primates, we administered the humanized monoclonal antibody targeting Siglec-15, 25E9, to estrogen-deficient female cynomolgus monkeys.
Two intravenous injections of vehicle (PBS) or 25E9 at 10 mg/kg were administered to two groups at an 8-week interval with a follow-up period of 6 months. Estrogen deficiency was induced by the repeated subcutaneous administration of a gonadotropin-releasing hormone agonist every 4 weeks starting 3 months prior to administering 25E9 and throughout the follow-up period. Serum and urine samples were collected weekly to evaluate the bone resorption and formation biomarkers, determine the PK profile of AB-25E9 and monitor for the presence of antibody-drug antibodies (ADA).
Treatment with 25E9 rapidly decreased bone resorption biomarkers (urinary NTx, serum CTx and TRAP5b) by 30% to 45% demonstrating the anti-resorptive properties of 25E9. Strikingly, the bone formation biomarkers (osteocalcin and BSAP) did not rapidly decrease and were minimally affected. The decrease in the levels of bone resorption biomarkers began to attenuate at approximately Week 6, which coincided with the appearance of ADAs. Interestingly, this attenuation was not observed before Week 20 in animals where little or no ADAs were detected. In agreement with these findings, the decline in AB-25E9 serum concentrations was faster in animals in which ADAs were detected. In monkeys that were negative for ADAs, the terminal elimination half-life of 25E9 ranged between 5-12 days.
Taken together, the biomarker profiles presented here show that 25E9 has anti-resorptive activity and maintains bone formation estrogen-deficient cynomolgus monkeys. These results underscore the novel mechanism of action of 25E9 and highlight its potential for osteoclast-targeted therapy of bone-related diseases.
Our experiments in mice or monkeys also included groups treated with 30 mg/kg of the anti-Siglec-15 antibody. Surprisingly, this increase in dosage was not associated with added benefit. To the contrary, in some instances there was a decrease in the effect of the antibody at this dose compared to a dosage of 10 mg/kg.
REFERENCES
The entire content of the references listed in the present application is incorporated herein by reference.
Stuible M. et al., U.S. Provisional application No. 61/673,442 filed on Jul. 19, 2012. Stuible M. et al., U.S. Provisional application No. 61/777,049 filed on Mar. 12, 2013. Stuible M. et al., U.S. Provisional application No. 61/810,415 filed on Apr. 10, 2013. Sooknanan, R. R. et al., “Polynucleotides and polypeptide sequences involved in the process of bone remodelling”, international application No. PCT/CA2007/000210 (published on Aug. 23, 2007 under No. WO2007/093042). Tremblay, G. B. et al. “Siglec 15 Antibodies in Treating Bone Loss-Related Disease”, international application No. PCT/CA2010/001586 (published on Apr. 14, 2011 under No. WO2011/041894); Hiruma Y. et al., “Antibody Targeting Osteoclast-Related Protein Siglec-15”; U.S. Ser. No. 12/677,621 published on Aug. 19, 2010 under US2010/0209428A1; Hiruma Y. et al., “Anti-Siglec-15 Antibody”, U.S. Ser. No. 13/143,253 published on Nov. 3, 2011 under No. US2011/0268733A1; Watanabe, I. et al., “Antibody Targeting Osteoclast-Related Protein Siglec-15”, international application No. PCT/EP2011/005219 published on Apr. 12, 2012 under No. WO2012045481A2. Angata, T., T. Hayakawa, M. Yamanaka, A. Varki, and M. Nakamura. 2006. Discovery of Siglec-14, a novel sialic acid receptor undergoing concerted evolution with Siglec-5 in primates. FASEB J 20:1964-1973. Angata, T., Y. Tabuchi, K. Nakamura, and M. Nakamura. 2007. Siglec-15: an immune system Siglec conserved throughout vertebrate evolution. Glycobiology 17:838-846. Baron, R., S. Ferrari, and R. G. Russell. 2011. Denosumab and bisphosphonates: different mechanisms of action and effects. Bone 48:677-692. Blasius, A. L., M. Cella, J. Maldonado, T. Takai, and M. Colonna. 2006. Siglec-His an IPC-specific receptor that modulates type I IFN secretion through DAP12 . Blood 107:2474-2476. Blasius, A. L., and M. Colonna. 2006. Sampling and signaling in plasmacytoid dendritic cells: the potential roles of Siglec-H. Trends Immunol 27:255-260. Bonifacino, J. S., and L. M. Traub. 2003. Signals for sorting of transmembrane proteins to endosomes and lysosomes. Annu Rev Biochem 72:395-447. Boyle, W. J., W. S. Simonet, and D. L. Lacey. 2003. Osteoclast differentiation and activation. Nature 423:337-342. Crocker, P. R., J. C. Paulson, and A. Varki. 2007. Siglecs and their roles in the immune system. Nat Rev Immunol 7:255-266. Crocker, P. R., and P. Redelinghuys. 2008. Siglecs as positive and negative regulators of the immune system. Biochem Soc Trans 36:1467-1471. Hiruma, Y., T. Hirai, and E. Tsuda. 2011. Siglec-15, a member of the sialic acid-binding lectin, is a novel regulator for osteoclast differentiation. Biochem Biophys Res Commun 409:424-429. Humphrey, M. B., M. R. Daws, S. C. Spusta, E. C. Niemi, J. A. Torchia, L. L. Lanier, W. E. Seaman, and M. C. Nakamura. 2006. TREM2, a DAP12-associated receptor, regulates osteoclast differentiation and function. J Bone Miner Res 21:237-245. Ishida-Kitagawa, N., K. Tanaka, X. Bao, T. Kimura, T. Miura, Y. Kitaoka, K. Hayashi, M. Sato, M. Maruoka, T. Ogawa, J. Miyoshi, and T. Takeya. 2012. Siglec-15 regulates the formation of functional osteoclasts in concert with DNAX-activating protein of 12 KDa (DAP12). J Biol Chem Kaifu, T., J. Nakahara, M. Inui, K. Mishima, T. Momiyama, M. Kaji, A. Sugahara, H. Koito, A. Ujike-Asai, A. Nakamura, K. Kanazawa, K. Tan-Takeuchi, K. Iwasaki, W. M. Yokoyama, A. Kudo, M. Fujiwara, H. Asou, and T. Takai. 2003. Osteopetrosis and thalamic hypomyelinosis with synaptic degeneration in DAP12-deficient mice. J Clin Invest 111:323-332. Lanier, L. L. 2009. DAP10- and DAP12-associated receptors in innate immunity. Immunol Rev 227:150-160. Law, C. L., S. P. Sidorenko, K. A. Chandran, Z. Zhao, S. H. Shen, E. H. Fischer, and E. A. Clark. 1996. CD22 associates with protein tyrosine phosphatase 1C, Syk, and phospholipase C-gamma (1) upon B cell activation. J Exp Med 183:547-560. Liu, Q. Y., R. R. Sooknanan, L. T. Malek, M. Ribecco-Lutkiewicz, J. X. Lei, H. Shen, B. Lach, P. R. Walker, J. Martin, and M. Sikorska. 2006. Novel subtractive transcription-based amplification of mRNA (STAR) method and its application in search of rare and differentially expressed genes in AD brains. BMC Genomics 7:286. Mao, D., H. Epple, B. Uthgenannt, D. V. Novack, and R. Faccio. 2006. PLCgamma2 regulates osteoclastogenesis via its interaction with ITAM proteins and GAB2 . J Clin Invest 116:2869-2879. Muhlbauer, R. C., F. Bauss, R. Schenk, M. Janner, E. Bosies, K. Strein, and H. Fleisch. 1991. BM 21.0955, a potent new bisphosphonate to inhibit bone resorption. J Bone Miner Res 6:1003-1011. O'Reilly, M. K., and J. C. Paulson. 2009. Siglecs as targets for therapy in immune-cell-mediated disease. Trends Pharmacol Sci 30:240-248. Paloneva, J., M. Kestila, J. Wu, A. Salminen, T. Bohling, V. Ruotsalainen, P. Hakola, A. B. Bakker, J. H. Phillips, P. Pekkarinen, L. L. Lanier, T. Timonen, and L. Peltonen. 2000. Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts. Nat Genet. 25:357-361. Park-Wyllie, L. Y., M. M. Mamdani, D. N. Juurlink, G. A. Hawker, N. Gunraj, P. C. Austin, D. B. Whelan, P. J. Weiler, and A. Laupacis. 2011. Bisphosphonate use and the risk of subtrochanteric or femoral shaft fractures in older women. JAMA 305:783-789. Raggatt, L. J., and N. C. Partridge. 2010. Cellular and molecular mechanisms of bone remodeling. J Biol Chem 285:25103-25108. Reid, I. R., and J. Cornish. 2011. Epidemiology and pathogenesis of osteonecrosis of the jaw. Nat Rev Rheumatol 8:90-96. Roelofs, A. J., K. Thompson, S. Gordon, and M. J. Rogers. 2006. Molecular mechanisms of action of bisphosphonates: current status. Clin Cancer Res 12:6222s-6230s. Sooknanan, R. R., G. B. Tremblay, and M. Filion. 2011. Polynucleotides and polypeptide sequences involved in the process of bone remodeling. U.S. Pat. No. 7,989,160. Takahata, M., N. Iwasaki, H. Nakagawa, Y. Abe, T. Watanabe, M. Ito, T. Majima, and A. Minami. 2007. Sialylation of cell surface glycoconjugates is essential for osteoclastogenesis. Bone 41:77-86. Taylor, V. C., C. D. Buckley, M. Douglas, A. J. Cody, D. L. Simmons, and S. D. Freeman. 1999. The myeloid-specific sialic acid-binding receptor, CD33, associates with the protein-tyrosine phosphatases, SHP-1 and SHP-2 . J Biol Chem 274:11505-11512. Tomasello, E., and E. Vivier. 2005. KARAP/DAP12/TYROBP: three names and a multiplicity of biological functions. Eur J Immunol 35:1670-1677. Toyomura, T., Y. Murata, A. Yamamoto, T. Oka, G. H. Sun-Wada, Y. Wada, and M. Futai. 2003. From lysosomes to the plasma membrane: localization of vacuolar-type H+-ATPase with the a3 isoform during osteoclast differentiation. J Biol Chem 278:22023-22030. Turnbull, I. R., and M. Colonna. 2007. Activating and inhibitory functions of DAP12 . Nat Rev Immunol 7:155-161. Underhill, D. M., and H. S. Goodridge. 2007. The many faces of ITAMs. Trends Immunol 28:66-73. Walker, J. A., and K. G. Smith. 2008. CD22: an inhibitory enigma. Immunology 123:314-325. Walsh, M. C., and Y. Choi. 2003. Biology of the TRANCE axis. Cytokine Growth Factor Rev 14:251-263.

Sequences


Note: Underlined sequences represent the constant region, twice-underlined sequences represent the signal sequence and sequences in bold represent complementarity determining regions.
(human Siglec-15 cDNA) SEQ ID NO: 1 ATGGAAAAGTCCATCTGGCTGCTGGCCTGCTTGGCGTGGGTTCTCCCGACAGGCTCATTTGTGAGA ACTAAAATAGATACTACGGAGAACTTGCTCAACACAGAGGTGCACAGCTCGCCAGCGCAGCGCTGG TCCATGCAGGTGCCACCCGAGGTGAGCGCGGAGGCAGGCGACGCGGCAGTGCTGCCCTGCACCTTC ACGCACCCGCACCGCCACTACGACGGGCCGCTGACGGCCATCTGGCGCGCGGGCGAGCCCTATGCG GGCCCGCAGGTGTTCCGCTGCGCTGCGGCGCGGGGCAGCGAGCTCTGCCAGACGGCGCTGAGCCTG CACGGCCGCTTCCGGCTGCTGGGCAACCCGCGCCGCAACGACCTCTCGCTGCGCGTCGAGCGCCTC GCCCTGGCTGACGACCGCCGCTACTTCTGCCGCGTCGAGTTCGCCGGCGACGTCCATGACCGCTAC GAGAGCCGCCACGGCGTCCGGCTGCACGTGACAGCCGCGCCGCGGATCGTCAACATCTCGGTGCTG CCCAGTCCGGCTCACGCCTTCCGCGCGCTCTGCACTGCCGAAGGGGAGCCGCCGCCCGCCCTCGCC TGGTCCGGCCCGGCCCTGGGCAACAGCTTGGCAGCCGTGCGGAGCCCGCGTGAGGGTCACGGCCAC CTAGTGACCGCCGAACTGCCCGCACTGACCCATGACGGCCGCTACACGTGTACGGCCGCCAACAGC CTGGGCCGCTCCGAGGCCAGCGTCTACCTGTTCCGCTTCCATGGCGCCAGCGGGGCCTCGACGGTC GCCCTCCTGCTCGGCGCTCTCGGCTTCAAGGCGCTGCTGCTGCTCGGGGTCCTGGCCGCCCGCGCT GCCCGCCGCCGCCCAGAGCATCTGGACACCCCGGACACCCCACCACGGTCCCAGGCCCAGGAGTCC AATTATGAAAATTTGAGCCAGATGAACCCCCGGAGCCCACCAGCCACCATGTGCTCACCGTGA (Human Siglec-15 polypeptide: 1-328) SEQ ID NO: 2 MEKSIWLLACLAWVLPTGSFVRTKIDTTENLLNTEVHSSPAQRWSMQVPPEVSAEAGDAAVLPCTF THPHRHYDGPLTAIWRAGEPYAGPQVFRCAAARGSELCQTALSLHGRFRLLGNPRRNDLSLRVERL ALADDRRYFCRVEFAGDVHDRYESRHGVRLHVTAAPRIVNISVLPSPAHAFRALCTAEGEPPPALA WSGPALGNSLAAVRSPREGHGHLVTAELPALTHDGRYTCTAANSLGRSEASVYLFRFHGASGASTV ALLLGALGFKALLLLGVLAARAARRRPEHLDTPDTPPRSQAQESNYENLSQMNPRSPPATMCSP (mouse Siglec-15 cDNA) SEQ ID NO: 3 ATGGAGGGGTCCCTCCAACTCCTGGCCTGCTTGGCCTGTGTGCTCCAGATGGGATCCCTTGTGAAA ACTAGAAGAGACGCTTCGGGGGATCTGCTCAACACAGAGGCGCACAGTGCCCCGGCGCAGCGCTGG TCCATGCAGGTGCCCGCGGAGGTGAACGCGGAGGCTGGCGACGCGGCGGTGCTGCCCTGCACCTTC ACGCACCCGCACCGCCACTACGACGGGCCGCTGACGGCCATCTGGCGCTCGGGCGAGCCGTACGCG GGCCCGCAGGTGTTCCGCTGCACCGCGGCGCCGGGCAGCGAGCTGTGCCAGACGGCGCTGAGCCTG CACGGCCGCTTCCGCCTGCTGGGCAACCCGCGCCGCAACGACCTGTCCCTGCGCGTCGAGCGCCTC GCCCTGGCGGACAGCGGCCGCTACTTCTGCCGCGTGGAGTTCACCGGCGACGCCCACGATCGCTAT GAGAGTCGCCATGGGGTCCGTCTGCGCGTGACTGCAGCTGCGCCGCGGATCGTCAACATCTCGGTG CTGCCGGGCCCCGCGCACGCCTTCCGCGCGCTCTGCACCGCCGAGGGGGAGCCCCCGCCCGCCCTC GCCTGGTCGGGTCCCGCCCCAGGCAACAGCTCCGCTGCCCTGCAGGGCCAGGGTCACGGCTACCAG GTGACCGCCGAGTTGCCCGCGCTGACCCGCGACGGCCGCTACACGTGCACGGCGGCCAATAGCCTG GGCCGCGCCGAGGCCAGCGTCTACCTGTTCCGCTTCCACGGCGCCCCCGGAACCTCGACCCTAGCG CTCCTGCTGGGCGCGCTGGGCCTCAAGGCCTTGCTGCTGCTTGGCATTCTGGGAGCGCGTGCCACC CGACGCCGACTAGATCACCTGGTCCCCCAGGACACCCCTCCACGGTCTCAGGCTCAGGAGTCCAAT TATGAAAATTTGAGCCAGATGAGTCCTCCAGGCCACCAGCTGCCACGTGTTTGCTGTGAGGAACTC CTCAGCCATCACCATCTAGTCATTCACCATGAGAAATAA (mouse Siglec-15 polypeptide) SEQ ID NO: 4 MEGSLQLLACLACVLQMGSLVKTRRDASGDLLNTEAHSAPAQRWSMQVPAEVNAEAGDAAVLPCTF THPHRHYDGPLTAIWRSGEPYAGPQVFRCTAAPGSELCQTALSLHGRFRLLGNPRRNDLSLRVERL ALADSGRYFCRVEFTGDAHDRYESRHGVRLRVTAAAPRIVNISVLPGPAHAFRALCTAEGEPPPAL AWSGPAPGNSSAALQGQGHGYQVTAELPALTRDGRYTCTAANSLGRAEASVYLFRFHGAPGTSTLA LLLGALGLKALLLLGILGARATRRRLDHLVPQDTPPRSQAQESNYENLSQMSPPGHQLPRVCCEEL LSHHHLVIHHEK 25E9 Light (Kappa) Chain Chimeric (mouse variable domain and human constant region) SEQ ID No.: 5 MVLQTQVFISLLLWISGAYG DIVMTQAAPSVPVTPGESVSISCRSTKSLLHSNGNTYLYWFLQRPG QSPQLLIYRMSNLASGVPDRFSGSGSGTAFTLRISRVEAEDVGVYYCMQHLEYPFTFGGGTKLEIK RTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTY SLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC 25E9 Light Chain mouse variable domain (illustrated without signal sequence: CDRs are in bold) SEQ ID No.: 6 DIVMTQAAPSVPVTPGESVSISC RSTKSLLHSNGNTYLY WFLQRPGQSPQLLIY RMSNLAS GVPDR FSGSGSGTAFTLRISRVEAEDVGVYYC MQHLEYPFT FGGGTKLEIK 25E9 Light (Kappa) Chain Humanized Variant 1 (a.k.a.: L1) (humanized variable domain and human constant region) SEQ ID NO.: 7 MVLQTQVFISLLLWISGAYG DIVMTQSPLSLPVTPGEPASISCRSTKSLLHSNGNTYLYWYLQKPG QSPQLLIYRMSNLASGVPDRFSGSGSGTDFTLKISRVEAEDVGVYYCMQHLEYPFTFGGGTKVEIK RTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTY SLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC 25E9 Light Chain Humanized Variant 1 variable domain (a.k.a.: VL1) (illustrated without signal sequence) SEQ ID NO.: 8 DIVMTQSPLSLPVTPGEPASISCRSTKSLLHSNGNTYLYWYLQKPGQSPQLLIYRMSNLASGVPDR FSGSGSGTDFTLKISRVEAEDVGVYYCMQHLEYPFTFGGGTKVEIK 25E9 Light (Kappa) Chain Humanized Variant 2 (a.k.a.: L2) (humanized variable domain and human constant region) SEQ ID NO.: 9 MVLQTQVFISLLLWISGAYG DIVMTQSPLSLPVTPGEPASISCRSTKSLLHSNGNTYLYWFLQKPG QSPQLLIYRMSNLASGVPDRFSGSGSGTDFTLKISRVEAEDVGVYYCMQHLEYPFTFGGGTKVEIK RTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTY SLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC 25E9 Light Chain Humanized Variant 2 variable domain (a.k.a.: VL2) (illustrated without signal sequence) SEQ ID NO.: 10 DIVMTQSPLSLPVTPGEPASISCRSTKSLLHSNGNTYLYWFLQKPGQSPQLLIYRMSNLASGVPDR FSGSGSGTDFTLKISRVEAEDVGVYYCMQHLEYPFTFGGGTKVEIK 25E9 Heavy (Igg1) Chain Chimeric (mouse variable domain and human constant region) SEQ ID NO.: 11 MDWTWRILFLVAAATGTHA EIQLQQSGVELVRPGASVTLSCKASGYTFTDYDMHWVKQTPVHGLEW IGTIDPETGGTAYNQKFKGKATLTADRSSTTAYMELSSLTSEDSAVYYCTSFYYTYSNYDVGFAYW GQGTLVTVSA ASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAV LQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPS VFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSV LTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKG FYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYT QKSLSLSPGK 25E9 Heavy Chain mouse variable domain (illustrated without signal sequence: CDRs are in bold) SEQ ID NO.: 12 EIQLQQSGVELVRPGASVTLSCKAS GYTFTDIDMH WVKQTPVHGLEWIG TIDPETGGTAYNQKFKG KATLTADRSSTTAYMELSSLTSEDSAVYYCTS FYYTYSNYDVGFAY WGQGTLVTVSA 25E9 Heavy (Igg1) Chain Humanized Variant 1 (a.k.a.: H1) (humanized variable domain and human constant region) SEQ ID NO.: 13 MDWTWRILFLVAAATGTHA EIQLQQSGAEVKKPGSSVKVSCKASGYTFTDYDMHWVRQAPGQGLEW MGTIDPETGGTAYNQKFKGRVTITADKSTSTAYMELSSLRSEDTAVYYCTSFYYTYSNYDVGFAYW GQGTLVTVSS ASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAV LQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPS VFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSV LTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKG FYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYT QKSLSLSPGK 25E9 Heavy Chain Humanized Variant 1 variable domain (a.k.a., VH1) (illustrated without signal sequence) SEQ ID NO.: 14 EIQLQQSGAEVKKPGSSVKVSCKASGYTFTDYDMHWVRQAPGQGLEWMGTIDPETGGTAYNQKFKG RVTITADKSTSTAYMELSSLRSEDTAVYYCTSFYYTYSNYDVGFAYWGQGTLVTVSS 25E9 Heavy (Igg1) Chain Humanized Variant 2 (a.k.a.: H2) (humanized variable domain and human constant region) SEQ ID NO.: 15 MDWTWRILFLVAAATGTHA EIQLQQSGAEVKKPGSSVKVSCKASGYTFTDYDMHWVRQAPGQGLEW IGTIDPETGGTAYNQKFKGRATLTADRSTSTAYMELSSLRSEDTAVYYCTSFYYTYSNYDVGFAYW GQGTLVTVSS ASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAV LQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPS VFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSV LTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKG FYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVESCSVMHEALHNHYT QKSLSLSPGK 25E9 Heavy Chain Humanized Variant 2 variable domain (a.k.a., VH2) (illustrated without signal sequence) SEQ ID NO.: 16 EIQLQQSGAEVKKPGSSVKVSCKASGYTFTDYDMHWVRQAPGQGLEWIGTIDPETGGTAYNQKFKG RATLTADRSTSTAYMELSSLRSEDTAVYYCTSFYYTYSNYDVGFAYWGQGTLVTVSS 25E9 Heavy (Igg1) Chain Humanized Variant 3 (a.k.a.: H3) (humanized variable domain and human constant region) SEQ ID NO.: 17 MDWTWRILFLVAAATGTHA EIQLQQSGAEVKKPGSSVKVSCKASGYTFTDYDMHWVKQAPGQGLEW IGTIDPETGGTAYNQKFKGKATLTADRSTSTAYMELSSLRSEDTAVYYCTSFYYTYSNYDVGFAYW GQGTLVTVSS ASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAV LQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPS VFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSV LTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKG FYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVESCSVMHEALHNHYT QKSLSLSPGK 25E9 Heavy Chain Humanized Variant 3 variable domain (a.k.a.: VH3) (illustrated without signal sequence) SEQ ID NO.: 18 EIQLQQSGAEVKKPGSSVKVSCKASGYTFTDYDMHWVKQAPGQGLEWIGTIDPETGGTAYNQKFKG KATLTADRSTSTAYMELSSLRSEDTAVYYCTSFYYTYSNYDVGFAYWGQGTLVTVSS 25E9 Heavy (Igg1) Chain Humanized Variant 4 (a.k.a.: H4) (humanized variable domain and human constant region) SEQ ID NO.: 19 MDWTWRILFLVAAATGTHA EIQLQQSGAEVKKPGSSVKVSCKASGYTFTDYDMHWVKQAPGHGLEW IGTIDPETGGTAYNQKFKGKATLTADRSTSTAYMELSSLTSEDTAVYYCTSFYYTYSNYDVGFAYW GQGTLVTVSS ASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAV LQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPS VFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSV LTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKG FYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYT QKSLSLSPGK 25E9 Heavy Chain Humanized Variant 4 variable domain (a.k.a.: VH4) (illustrated without signal sequence) SEQ ID NO.: 20 EIQLQQSGAEVKKPGSSVKVSCKASGYTFTDYDMHWVKQAPGHGLEWIGTIDPETGGTAYNQKFKG KATLTADRSTSTAYMELSSLTSEDTAVYYCTSFYYTYSNYDVGFAYWGQGTLVTVSS Chimeric 25D8 Light (Kappa) Chain (mouse variable domain and human constant region) SEQ ID NO.: 21 MVLQTQVFISLLLWISGAYG DIVMTQAAFSNPVTLGTSASISCRSSKSLLHSNGITYLYWYLQKPG QSPQLLIYQMSNLASGVPDRFSSSGSGTDFTLRISRVEAEDVGVYYCAQNLELPYTFGGGTKLEIK RTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTY SLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC 25D8 Light Chain mouse variable domain (illustrated without signal sequence) SEQ ID NO.: 22 DIVMTQAAFSNPVTLGTSASISC RSSKSLLHSNGITYLY WYLQKPGQSPQLLIY QMSNLASG VPDR FSSSGSGTDFTLRISRVEAEDVGVYYC AQNLELPYT FGGGTKLEIK Humanized 25D8 Light (Kappa) Chain (humanized variable domain and human constant region) SEQ ID NO.: 23 MVLQTQVFISLLLWISGAYG DIVMTQTPLSLPVTPGEPASISCRSSKSLLHSNGITYLYWYLQKPG QSPQLLIYQMSNLASGVPDRFSGSGSGTDFTLKISRVEAEDVGVYYCAQNLELPYTFGGGTKVEIK RTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTY SLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC Humanized 25D8 Light Chain variable domain (illustrated without signal sequence) SEQ ID NO.: 24 DIVMTQTPLSLPVTPGEPASISCRSSKSLLHSNGITYLYWYLQKPGQSPQLLIYQMSNLASGVPDR FSGSGSGTDFTLKISRVEAEDVGVYYCAQNLELPYTFGGGTKVEIK Chimeric 25D8 Heavy (Igg2) Chain (mouse variable domain and human constant region) SEQ ID NO.: 25 MDWTWRILFLVAAATGTHA QVQVQQPGAELVKPGASVKLSCKASGYTFTSYWMHWVKQRPGQGLEW IGLINPSNARTNYNEKENTKATLTVDKSSSTAYMQLSSLTSEDSAVYYCARGGDGDYFDYWGQGTT LTVSS ASTKGPSVFPLAPCSRSTSESTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSG LYSLSSVVTVPSSNFGTQTYTCNVDHKPSNTKVDKTVERKCCVECPPCPAPPVAGPSVFLFPPKPK DTLMISRTPEVTCVVVDVSHEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTFRVVSVLTVVHQDWL NGKEYKCKVSNKGLPAPIEKTISKTKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVE WESNGQPENNYKTTPPMLDSDGSFFLYSKLTVDKSRWQQGNVESCSVMHEALHNHYTQKSLSLSPG K 25D8 Heavy Chain mouse variable domain (illustrated without signal sequence) SEQ ID NO.: 26 QVQVQQPGAELVKPGASVKLSCKAS GYTFTSYWMH WVKQRPGQGLEWIG LINPSNARTNYNEKFNT KATLTVDKSSSTAYMQLSSLTSEDSAVYYCAR GGDGDYFDY WGQGTTLTVSS Humanized 25D8 Heavy (Igg2) Chain (humanized variable domain and human constant region) SEQ ID NO.: 27 MDWTWRILFLVAAATGTHA QVQLQQSGAEVKKPGSSVKVSCKASGYTFTSYWMHWVRQAPGQGLEW MGLINPSNARTNYNEKENTRVTITADKSTSTAYMELSSLRSEDTAVYYCARGGDGDYFDYWGQGTT VTVSS ASTKGPSVFPLAPCSRSTSESTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSG LYSLSSVVTVPSSNFGTQTYTCNVDHKPSNTKVDKTVERKCCVECPPCPAPPVAGPSVFLFPPKPK DTLMISRTPEVTCVVVDVSHEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTFRVVSVLTVVHQDWL NGKEYKCKVSNKGLPAPIEKTISKTKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVE WESNGQPENNYKTTPPMLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPG K Humanized 25D8 Heavy Chain variable domain (illustrated without signal sequence) SEQ ID NO.: 28 QVQLQQSGAEVKKPGSSVKVSCKASGYTFTSYWMHWVRQAPGQGLEWMGLINPSNARTNYNEKFNT RVTITADKSTSTAYMELSSLRSEDTAVYYCARGGDGDYFDYWGQGTTVTVSS 25E9 Heavy (Igg2) Chain Humanized Variant 1 (humanized variable domain and human constant region) SEQ ID NO. 29 MDWTWRILFLVAAATGTHA EIQLQQSGAEVKKPGSSVKVSCKASGYTFTDYDMHWVRQAPGQGLEW MGTIDPETGGTAYNQKFKGRVTITADKSTSTAYMELSSLRSEDTAVYYCTSFYYTYSNYDVGFAYW GQGTLVTVSS ASTKGPSVFPLAPCSRSTSESTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAV LQSSGLYSLSSVVTVPSSNFGTQTYTCNVDHKPSNTKVDKTVERKCCVECPPCPAPPVAGPSVFLF PPKPKDTLMISRTPEVTCVVVDVSHEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTFRVVSVLTVV HQDWLNGKEYKCKVSNKGLPAPIEKTISKTKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPS DIAVEWESNGQPENNYKTTPPMLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSL SLSPGK 25E9 Heavy (Igg2) Chain Chimeric (mouse variable domain and human constant region) SEQ ID No.: 30 MDWTWRILFLVAAATGTHA EIQLQQSGVELVRPGASVTLSCKASGYTFTDYDMHWVKQTPVHGLEW IGTIDPETGGTAYNQKFKGKATLTADRSSTTAYMELSSLTSEDSAVYYCTSFYYTYSNYDVGFAYW GQGTLVTVSA ASTKGPSVFPLAPCSRSTSESTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAV LQSSGLYSLSSVVTVPSSNFGTQTYTCNVDHKPSNTKVDKTVERKCCVECPPCPAPPVAGPSVFLF PPKPKDTLMISRTPEVTCVVVDVSHEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTFRVVSVLTVV HQDWLNGKEYKCKVSNKGLPAPIEKTISKTKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPS DIAVEWESNGQPENNYKTTPPMLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSL SLSPGK (human IgG1 constant region) SEQ ID NO.: 31 ASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLS SVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFPPKPKD TLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWLN GKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSDIAVEW ESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK (human IgG2 constant region) SEQ ID NO.: 32 ASTKGPSVFPLAPCSRSTSESTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLS SVVTVPSSNFGTQTYTCNVDHKPSNTKVDKTVERKCCVECPPCPAPPVAGPSVFLFPPKPKDTLMI SRTPEVTCVVVDVSHEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTFRVVSVLTVVHQDWLNGKEY KCKVSNKGLPAPIEKTISKTKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNG QPENNYKTTPPMLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK Generic 25E9 light chain variable domain (consensus 1) SEQ ID No. 33 DIVMTQXXXSXPVTPGEXXSISCRSTKSLLHSNGNTYLYWXLQXPGQSPQLLIYRMSNLASGVPDR FSGSGSGTXFTLXISRVEAEDVGVYYCMQHLEYPFTFGGGTKXEIK
wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:6 (the mouse VL). The amino acid substitution may be, for example conservative or non-conservative. In accordance with the invention, the amino acid substitution may be conservative.

Generic 25E9 light chain variable domain (consensus 2) SEQ ID No. 34 DIVMTQX a1 X a2 X a3 SX a4 PVTPGEX a5 X a6 SISCRSTKSLLHSNG NTYLYWX a7 LQX a8 PGQSPQLLIYRMSNLASGVPDRFSGSGSG TX a9 FTLX a10 ISRVEAEDVGVYYCMQHLEYPFTFGGGTKX a11 EIK
wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:6 (the mouse VL) and Wherein Xa1, Xa4, Xa7, Xa8, Xa10 and Xa11 may each independently be a conservative amino acid substitution in comparison with SEQ ID NO. 6;

Wherein Xa2, Xa5, Xa6 may each independently be a semi-conservative amino acid substitution in comparison with SEQ ID NO. 6;

Wherein Xa3 may be P or L; and

Wherein Xa9 may be A or D.

Generic 25E9 light chain variable domain (consensus 3) SEQ ID NO. 35 DIVMTQX a1 X a2 X a3 SX a4 PVTPGEX a5 X a6 SISCRSTKSLLHSNG NTYLYWX a7 LQX a8 PGQSPQLLIYRMSNLASGVPDRFSGSGSG TX a9 FTLX a10 ISRVEAEDVGVYYCMQHLEYPFTFGGGTKX a11 EIK
wherein at least one of the amino acid identified by X (including Xa1 to Xa11) may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:6 (the mouse VL) and

Wherein Xa1 may be A or S;

Wherein Xa2 may be A or P;

Wherein Xa3 may be P or L;

Wherein Xa4 may be a hydrophobic amino acid (e.g., V or L);

Wherein Xa5 may be S or P;

Wherein Xa6 may be a hydrophobic amino acid (e.g., V or A);

Wherein Xa7 may be an aromatic amino acid (e.g. F or Y);

Wherein Xa8 may be a basic amino acid (e.g., R or K);

Wherein Xa9 may be A or D;

Wherein Xa10 may be a basic amino acid (e.g., R or K);

and wherein Xa11 may be a hydrophobic amino acid (e.g., L or V).

Generic 25E9 heavy chain variable domain (consensus 1) SEQ ID NO. 36 EIQLQQSGXEXXXPGXSVXXSCKASGYTFTDYDMHWVXQXPX XGLEWXGTIDPETGGTAYNQKFKGXXTXTADXSXXTAYMELS SLXSEDXAVYYCTSFYYTYSNYDVGFAYWGQGTLVTVSX
wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:12 (the mouse VH). The amino acid substitution may be, for example conservative or non-conservative. In accordance with the invention, the amino acid substitution may be conservative.

Generic 25E9 heavy chain variable domain (consensus 2) SEQ ID NO. 37 EIQLQQSGX b1 EX b2 X b3 X b4 PGX b5 SVX b6 X b7 SCKASGYTFTDY DMHWVX b8 QX b9 Px b10 X b11 GLEWX b12 GTIDPETGGTAYNQKFK GX b13 X b14 TX b15 TADX b16 SX b17 X b18 TAYMELSSLX b19 SEDX b20 AVYYCTSFYYTYSNYDVGFAYWGQGTLVTVSX b21
wherein at least one of the amino acid identified by X (including Xb1 to Xb21) may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:12 (the mouse VH) and

wherein Xb2, Xb4, Xb5, Xb7, Xb8, Xb9, Xb11, Xb12, Xb13, Xb15, Xb16, Xb17, Xb18, Xb20 and Xb21 may each independently be a conservative amino acid substitution in comparison with SEQ ID NO. 12;

wherein Xb1, Xb6, Xb14 may each independently be a semi-conserved amino acid substitution in comparison with SEQ ID NO.:12 (the mouse VH)

wherein Xb3 may be V or K;

wherein Xb10 may be V or G; and

wherein Xb19 may be T or R.

Generic 25E9 heavy chain variable domain (consensus 3) SEQ ID NO. 38 EIQLQQSGX b1 EX b2 X b3 X b4 PGX b5 SVX b6 X b7 SCKASGYTFTDY DMHWVX b8 QX b9 Px b10 X b11 GLEWX b12 GTIDPETGGTAYNQKFK GX b13 X b14 TX b15 TADX b16 SX b17 X b18 TAYMELSSLX b19 SEDX b20 AVYYCTSFYYTYSNYDVGFAYWGQGTLVTVSX b21
wherein at least one of the amino acid identified by X (including Xb1 to Xb21) may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:12 (the mouse VH) and

wherein Xb1 may be a hydrophobic amino acid (e.g., V or A);

wherein Xb2 may be a hydrophobic amino acid (e.g., L or V);

wherein Xb3 may be V or K;

wherein Xb4 may be a basic amino acid (e.g., R or K);

Wherein Xb5 may be A or S;

Wherein Xb6 may be T or K;

Wherein Xb7 may be a hydrophobic amino acid (e.g., L or V);

Wherein Xb8 may be a basic amino acid (e.g., K or R);

Wherein Xb9 may be T or A;

wherein Xb10 may be V or G;

Wherein Xb11 may be a basic amino acid (e.g., H or Q);

Wherein Xb12 may be a hydrophobic amino acid (e.g., I or M);

Wherein Xb13 may be a basic amino acid (e.g., K or R);

Wherein Xb14 may be a hydrophobic amino acid (e.g., A or V);

Wherein Xb15 may be a hydrophobic amino acid (e.g., L or I);

Wherein Xb16 may be a basic amino acid (e.g., R or K);

Wherein Xb17 may be a neutral hydrophilic amino acid (e.g., S or T);

Wherein Xb18 may be a neutral hydrophilic amino acid (e.g., T or S);

wherein Xb19 may be T or R;

Wherein Xb20 may be a neutral hydrophilic amino acid (e.g., S or T); and

Wherein Xb21 may be A or S.

Generic 25D8 light chain variable domain (consensus 1) SEQ ID No.: 39 DIVMTQXXXSXPVTXGXXASISCRSSKSLLHSNGITYLYWY LQKPGQSPQLLIYQMSNLASGVPDRFSXSGSGTDFTLXISR VEAEDVGVYYCAQNLELPYTFGGGTKXEIK
wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:22 (the mouse VL). The amino acid substitution may be, for example conservative or non-conservative. In accordance with the invention, the amino acid substitution may be conservative.

Generic 25D8 light chain variable domain (consensus 2) SEQ ID NO.: 40 DIVMTQX c1 X c2 X c3 SX c4 PVTX c5 GX c6 X c7 ASISCRSSKSLLHS NGITYLYWYLQKPGQSPQLLIYQMSNLASGVPDRFSX c8 SGS GTDFTLX c9 ISRVEAEDVGVYYCAQNLELPYTFGGGTKX c10 E IK
wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:22 (the mouse VL) and

wherein Xc1, Xc3, Xc9 and Xc10 may each independently be a conservative amino acid substitution in comparison with SEQ ID NO.:22;

wherein Xc2, Xc7, Xc8 may each independently be a semi-conservative amino acid substitution in comparison with SEQ ID NO.: 22;

Wherein Xc4 may be N or L;

Wherein Xc5 may be L or P; and

Wherein Xc6 may be T or E.

Generic 25D8 light chain variable domain (consensus 3) SEQ ID NO.: 41 DIVMTQX c1 X c2 X c3 SX c4 PVTX c5 GX c6 X c7 ASISCRSSKSLLHS NGITYLYWYLQKPGQSPQLLIYQMSNLASGVPDRFSX c8 SGS GTDFTLX c9 ISRVEAEDVGVYYCAQNLELPYTFGGGTKX c10 E IK
wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:22 (the mouse VL) and

Wherein Xc1 may be A or T;

Wherein Xc2 may be A or P;

Wherein Xc3 may be F or L;

Wherein Xc4 may be N or L;

Wherein Xc5 may be L or P;

Wherein Xc6 may be T or E;

Wherein Xc7 may be S or P;

Wherein Xc8 may be S or G;

Wherein Xc9 may be a basic amino acid (e.g., R or K); and

Wherein Xc10 may be a hydrophobic amino acid (e.g., L or V).

Generic 25D8 heavy chain variable domain (consensus 1) SEQ ID NO.: 42 QVQXQQXGAEXXKPGXSVKXSCKASGYTFTSYWMHWVXQXP GQGLEWXGLINPSNARTNYNEKFNTXXTXTXDKSXSTAYMX LSSLXSEDXAVYYCARGGDGDYFDYWGQGTTXTVSS
wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:26 (the mouse VH). The amino acid substitution may be, for example conservative or non-conservative. In accordance with the invention, the amino acid substitution may be conservative.

Generic 25D8 heavy chain variable domain (consensus 2) SEQ ID NO.: 43 QVQX d1 QQX d2 GAEX d3 X d4 KPGX d5 SVKX d6 SCKASGYTFTSYWM HWVX d7 QX d8 PGQGLEWX d9 GLINPSNARTNYNEKFNTX d10 X d11 TX d12 TX d13 DKSX d14 STAYMX d15 LSSLX d16 SEDX d17 AVYYCAR GGDGDYFDYWGQGTTX d18 TVSS
wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:26 (the mouse VH) and;

wherein Xd1, Xd3, Xd5, Xd6, Xd7, Xd9, Xd10, Xd12, Xd14, Xd15, Xd17, Xd18 may each independently be a conservative amino acid substitution in comparison with SEQ ID NO.:26;

wherein Xd2, Xd11, Xd13, may each independently be a semi-conservative amino acid substitution in comparison with SEQ ID NO.:26;

wherein Xd4 may be V or K;

wherein Xd8 may be R or A; and;

wherein Xd16 may be T or R.

Generic 25D8 heavy chain variable domain (consensus 3) SEQ ID NO.: 44 QVQX d1 QQX d2 GAEX d3 X d4 KPGX d5 SVKX d6 SCKASGYTFTSYWM HWVX d7 QX d8 PGQGLEWX d9 GLINPSNARTNYNEKFNTX d10 X d11 TX d12 TX d13 DKSX d14 STAYMX d15 LSSLX d16 SEDX d17 AVYYCAR GGDGDYFDYWGQGTTX d18 TVSS
wherein at least one of the amino acid identified by X may be an amino acid substitution in comparison with a corresponding amino acid in the polypeptide set forth in SEQ ID NO.:26 (the mouse VH) and;

wherein Xd1 may be a hydrophobic amino acid (e.g., V or L);

wherein Xd2 may be P or S;

wherein Xd3 may be a hydrophobic amino acid (e.g., L or V);

wherein Xd4 may be V or K;

wherein Xd5 may be A or S;

wherein Xd6 may be a hydrophobic amino acid (e.g., L or V);

wherein Xd7 may be a basic amino acid (e.g., K or R);

wherein Xd8 may be R or A;

wherein Xd9 may be a hydrophobic amino acid (e.g., I or M);

wherein Xd10 may be a basic amino acid (e.g., K or R);

wherein Xd11 may be a hydrophobic amino acid (e.g., A or V);

wherein Xd12 may be a hydrophobic amino acid (e.g., L or I);

wherein Xd13 may be a hydrophobic amino acid (V or A);

wherein Xd14 may be a neutral hydrophilic amino acid (e.g., S or T);

wherein Xd15 may be Q or E;

wherein Xd16 may be T or R.

wherein Xd17 may be a neutral hydrophilic amino acid (e.g., S or T); and

wherein Xd18 may be a hydrophobic amino acid (L or V).







Chimeric 25D8 Heavy (Igg1) Chain (mouse variable domain and human


constant region)

SEQ ID NO.: 45


MDWTWRILFLVAAATGTHA QVQVQQPGAELVKPGASVKLSCKAS GYTFTSYWMH WVKQRPGQGLEW




IG LINPSNARTNYNEKFNT KATLTVDKSSSTAYMQLSSLTSEDSAVYYCAR GGDGDYFDY WGQGTT



LTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSG



LYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFP



PKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLH



QDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSD



IAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLS



LSPGK



Humanized 25D8 Heavy (Igg1) Chain (humanized variable domain and

human constant region)

SEQ ID NO.: 46


MDWTWRILFLVAAATGTHA QVQLQQSGAEVKKPGSSVKVSCKASGYTFTSYWMHWVRQAPGQGLEW




MGLINPSNARTNYNEKFNTRVTITADKSTSTAYMELSSLRSEDTAVYYCARGGDGDYFDYWGQGTT



VTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSG



LYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHTCPPCPAPELLGGPSVFLFP



PKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLH



QDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSRDELTKNQVSLTCLVKGFYPSD



IAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLS



LSPGK



CDR1 of the 25E9 light chain mouse variable domain

SEQ ID NO.: 47



RSTKSLLHSEGNTYLY





CDR2 of the 25E9 light chain mouse variable domain

SEQ ID NO.: 48



RMSNLAS





CDR3 of the 25E9 light chain mouse variable domain

SEQ ID NO.: 49



MQHLEYPFT





CDR1 of the 25E9 heavy chain mouse variable domain

SEQ ID NO.: 50



GYTFTDYDMH





CDR2 of the 25E9 heavy chain mouse variable domain

SEQ ID NO.: 51



TIDPETGGTAYNQKFKG





CDR3 of the 25E9 heavy chain mouse variable domain

SEQ ID NO.: 52



FYYTYSNYDVGFAY





CDR1 of the 25D8 light chain mouse variable domain

SEQ ID NO.: 53



RSSKSLLHSNGITYLY





CDR2 of the 25D8 light chain mouse variable domain

SEQ ID NO.: 54



QMSNLASG





CDR3 of the 25D8 light chain mouse variable domain

SEQ ID NO.: 55



AQNLELPYT





CDR1 of the 25D8 heavy chain mouse variable domain

SEQ ID NO.: 56



GYTFTSYWMH





CDR2 of the 25D8 heavy chain mouse variable domain

SEQ ID NO.: 57



LINPSNARTNYNEKFNT





CDR3 of the 25D8 heavy chain mouse variable domain

SEQ ID NO.: 58



GGDGDYFDY





25E9 Heavy (Igg2) Chain Humanized Variant 2 (a.k.a.: H2)

(humanized variable domain and human constant region)

SEQ ID NO.: 59


MDWTWRILFLVAAATGTHA EIQLQQSGAEVKKPGSSVKVSCKASGYTFTDYDMHWVRQAPGQGLEW




IGTIDPETGGTAYNQKFKGRATLTADRSTSTAYMELSSLRSEDTAVYYCTSFYYTYSNYDVGFAYW



GQGTLVTVSS ASTKGPSVFPLAPCSRSTSESTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAV




LQSSGLYSLSSVVTVPSSNFGTQTYTCNVDHKPSNTKVDKTVERKCCVECPPCPAPPVAGPSVFLF





PPKPKDTLMISRTPEVTCVVVDVSHEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTFRVVSVLTVV





HQDWLNGKEYKCKVSNKGLPAPIEKTISKTKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPS





DIAVEWESNGQPENNYKTTPPMLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSL





SLSPGK




25E9 Heavy (Igg2) Chain Humanized Variant 3 (a.k.a.: H3)

(humanized variable domain and human constant region)

SEQ ID NO.: 60


MDWTWRILFLVAAATGTHA EIQLQQSGAEVKKPGSSVKVSCKASGYTFTDYDMHWVKQAPGQGLEW




IGTIDPETGGTAYNQKFKGKATLTADRSTSTAYMELSSLRSEDTAVYYCTSFYYTYSNYDVGFAYW



GQGTLVTVSS ASTKGPSVFPLAPCSRSTSESTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAV




LQSSGLYSLSSVVTVPSSNFGTQTYTCNVDHKPSNTKVDKTVERKCCVECPPCPAPPVAGPSVFLF





PPKPKDTLMISRTPEVTCVVVDVSHEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTFRVVSVLTVV





HQDWLNGKEYKCKVSNKGLPAPIEKTISKTKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPS





DIAVEWESNGQPENNYKTTPPMLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSL





SLSPGK




25E9 Heavy (Igg2) Chain Humanized Variant 4 (a.k.a.: H4)

(humanized variable domain and human constant region)

SEQ ID NO.: 61


MDWTWRILFLVAAATGTHA EIQLQQSGAEVKKPGSSVKVSCKASGYTFTDYDMHWVKQAPGHGLEW




IGTIDPETGGTAYNQKFKGKATLTADRSTSTAYMELSSLTSEDTAVYYCTSFYYTYSNYDVGFAYW



GQGTLVTVSS ASTKGPSVFPLAPCSRSTSESTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAV




LQSSGLYSLSSVVTVPSSNFGTQTYTCNVDHKPSNTKVDKTVERKCCVECPPCPAPPVAGPSVFLF





PPKPKDTLMISRTPEVTCVVVDVSHEDPEVQFNWYVDGVEVHNAKTKPREEQFNSTFRVVSVLTVV





HQDWLNGKEYKCKVSNKGLPAPIEKTISKTKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPS





DIAVEWESNGQPENNYKTTPPMLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSL





SLSPGK




(nucleotide sequence of the 25E9 Light Chain mouse variable domain)

SEQ ID No.: 62


GATATTGTGATGACCCAGGCTGCACCCTCTGTACCTGTCACTCCTGGAGAGTCAGTATCCATCTCC




TGCAGGTCTACTAAGAGTCTCCTGCATAGTAATGGCAACACTTACTTGTATTGGTTCCTGCAGAGG



CCAGGCCAGTCTCCTCAGCTCCTGATATATCGGATGTCCAACCTTGCCTCAGGAGTCCCAGACAGG



TTCAGTGGCAGTGGGTCAGGAACTGCTTTCACACTGAGAATCAGTAGAGTGGAGGCTGAGGATGTG



GGTGTTTATTACTGTATGCAACATCTAGAATATCCTTTCACGTTCGGAGGGGGGACCAAGCTGGAA



ATAAAA



(nucleotide sequence of the 25E9 heavy Chain mouse variable domain)

SEQ ID NO: 63


GAGATCCAGCTGCAGCAGTCTGGAGTTGAGCTGGTGAGGCCTGGGGCTTCAGTGACGCTGTCCTGC




AAGGCTTCGGGCTACACATTTACTGACTATGACATGCACTGGGTGAAGCAGACACCTGTTCATGGC



CTGGAATGGATTGGAACTATTGATCCTGAAACTGGTGGTACTGCCTACAATCAGAAGTTCAAGGGC



AAGGCCACACTGACTGCGGACAGATCCTCCACCACAGCCTACATGGAGCTCAGCAGCCTGACATCT



GAGGACTCTGCCGTCTATTACTGTACAAGTTTCTACTATACTTACTCTAATTACGACGTGGGGTTT



GCTTACTGGGGCCAAGGGACTCTGGTCACTGTCTCTGCA



(nucleotide sequence of the humanized 25E9 light

chain variable domain-variant 1- illustrated without the portion

coding for the signal sequence)

SEQ ID NO.:64


gacatcgtgatgacccagtcccccctgtccctgcctgtgacacctggcgagcccgcctccatctcc




tgccggtccaccaagtccctgctgcactccaacggcaacacctacctgtactggtatctgcagaag



cccggccagtcccctcagctgctgatctaccggatgtccaacctggcctccggcgtgcccgacaga



ttctccggctctggctccggcaccgacttcaccctgaagatctcccgggtggaagccgaggacgtg



ggcgtgtactactgcatgcagcacctggaataccccttcaccttcggcggaggcaccaaggtggaa



atcaag



(nucleotide sequence of the humanized 25E9 heavy

chain variable domain-variant 1- illustrated without the portion

coding for the signal sequence)

SEQ ID NO.:65


gagattcagctgcagcagtcaggagccgaagtgaagaaacccggctccagcgtcaaggtgagttgc




aaggcctccggatacactttcaccgactatgatatgcactgggtgagacaggcacctgggcagggt



ctggagtggatggggaccatcgatccagaaaccggcggaacagcctacaaccagaagtttaaaggt



cgagtgacaattactgctgacaagtccaccagcacagcatatatggagctgtctagtctgcgttct



gaagatacagccgtctactattgcacttctttctactacacctacagtaactacgacgtggggttt



gcttactggggccagggaactctggtcaccgtgtcatcc



SEQ ID NO.: 66: candidate human model for 25D8 light chain variable

domain

DIVMTQTPLSLPVTPGEPASISC RSSQSLLHSEGYNYLD WYLQKPGQSPQLLIY LGSNRASG VPDR

FSGSGSGTDFTLKISRVEAEDVGVYYC MQGLQTPLT FGGGTKVEIK



SEQ ID NO.: 67: candidate human model for 25D8 light chain variable

domain

DIVMTQTPLSLPVTPGEPASISC RASQSLLHSNGYNYLD WYLQKPGQSPQLLIY LGSNRASG VPDR

FSGSGSGTDFTLRISRVEAEDVGVYYC MQGLQTPLT FGGGTKVEIK



SEQ ID NO.: 68: candidate human model for 25D8 light chain variable

domain

DIVMTQSPLSLSVTPGQPASISC KSSQSLLHSDGKTYLY WYLQKPGQPPQLLIY EVSNRFSG VPDR

FSGSGSGTDFTLKISRVEAEDVGVYYC MQSIQLPYT FGQGTKLEIK



SEQ ID NO.: 69: human model for 25D8 light chain variable domain

DIVMTQSPLSLPVTPGEPASISC RSSQSLLHSNGYNYLD WYLQKPGQSPQLLIY LGSNRASG VPDR

FSGSGSGTDFTLKISRVEAEDVGVYYC MQALQ



SEQ ID No.: 70: candidate human model for 25D8 light chain variable

domain

DIVMTQPPLSLPVTPGEPASISC RSSQSLLHSEGYNYLD WYLQKPGQSPQLLIY LGSNRASG VPDR

FSGSGSGTDFTLKISRVEAEDVGVYYC MQALQ



SEQ ID NO.: 71: candidate human model for 25D8 light chain variable

domain

DIVMTQTPLSLSVTPGQPASISC KSSQSLLHSDGKTYLY WYLQKPGQSPQLLIY EVSNRFSG VPDR

FSGSGSGTDFTLKISRVEAEDVGVYYC MQSIQL



SEQ ID NO.: 72: candidate human model for 25D8 light chain variable

domain

DIVMTQSPLSLPVTPGEPASISC RSSQSLLHSDGNNYLN WYLQKPGQSPQLLIY LVSNRASG VPDR

FSGSGSGTDFTLKISRVEAEDVGVYYC MQALQPRXT FGQGTKVEIK



SEQ ID NO.: 73: candidate human model for 25D8 heavy chain variable

domain

QVQLQQSGAEVKKPGSSVKVSCKAS GGTFGSYAIS WVRQAPGQGLEWMG RIIPILGIATYAQKFQG

RVTITADKSTSTAYMDLSSLRSEDTAVYYCAR GKGEFEGMDV WGQGTTVTVSS



SEQ ID NO.: 74: candidate human model for 25D8 heavy chain variable

domain

QVQLQQSGAEVKKPGSSVKVSCKAS GGTFSSYAIS WVRQAPGQGLEWMG RIIPILGIANYAQKFQG

RVTITADKSTSTAYMELSSLRSEDTAVYYCAR DTHSWFAFDI WGQGTMVTVSS



SEQ ID NO.: 75: candidate human model for 25D8 heavy chain variable

domain

EVOLVQSGAEMKKPGASVKVSCKAS GYSFSIYNIH WVRQAPGQGLEWMG WIHAGTGNRKYSQVFQD

RVTITRDTSASTSYMELSSLTSEDTAVYYCAR DPNFGDFDS WGQGTLVTVSS



SEQ ID NO.: 76: candidate human model for 25D8 heavy chain variable

domain

QVQLVQSGAEVKKPGSSVKVSCKAS GGTFSSYAIS WVRQAPGQGLEWMG GIIPIFGTANYAQKFQG

RVTITADESTSTAYMELSSLRSEDTAVYYCAR MYNWNFFDY WGQGTLVTVSS



SEQ ID NO.: 77: candidate human model for 25D8 heavy chain variable

domain

QVQLVQSGAEVKKPGASVKVSCKAS GYTFTSYYMH WVRQAPGQGLEWMG IINPSGGSTSYAQKFQG

RVTMTRDTSTSTVYMELSSLRSEDTAVYYCAR EGDGYIQAFDY WGQGTLVTVSS



SEQ ID NO.: 78: candidate human model for 25D8 heavy chain variable

domain

QVQLVQSGAEVKKPGSSVKVSCKAS GGTFSSYAIS WVRQAPGQGLEWMG GIIPIFGTANYAQKFQG

RVTITADKSTSTAYMELSSLRSEDTAVYYCAR



SEQ ID NO.: 79: candidate human model for 25D8 heavy chain variable

domain

QVQLVQSGAEVKKPGASVKVSCKAS GYTFTSYYMH WVRQAPGQGLEWMG IINPSGGSTSYAQKFQG

RVTMTRDTSTSTVYMELSSLRSEDTAVYYCAR



SEQ ID NO.: 80: candidate human model for 25D8 heavy chain variable

domain

QVQLVQSGAEVKKPGASVKVSCKAS GYTFTSYAIS WVRQAPGQGLEWMG WINPGNGDTNYAQKFQG

RVTITADTSTSTAYMELSSLRSEDTAVYYCAR GGRGDYFDY WGQGTLVTVSS



SEQ ID NO.: 81: candidate human model for 25E9 light chain variable

domain

DIVMTQSPLSLPVTPGEPASISC RSSQSLLHSTGNNYLD WYLQKPGQSPQLLIY LGSNRAS GVPDR

FSGSGSGTDFTLKISRVEAEDVGVYYC MQFLQTPLT FGGGTKVEIK



SEQ ID NO.: 82: candidate human model for 25E9 light chain variable

domain

DIVMTQTPLSLPVTPGEPASISC RASQSLLHSNGYNYLD WYLQKPGQSPQLLIY LGSNRAS GVPDR

FSGSGSGTDFTLRISRVEAEDVGVYYC MQGLQTPLT FGGGTKVEIK



SEQ ID NO.: 83: candidate human model for 25E9 light chain variable

domain

DIVMTQSPLSLPVTPGEPASISC RSSQSLLHSNGYNYLD WYLQKPGQSPQLLIY LGSNRAS GVPDR

FSGSGSGTDFTLKISRVEAEDVGVYYC MQALQ



SEQ ID NO.: 84: candidate human model for 25E9 light chain variable

domain

DIVMTQPPLSLPVTPGEPASIS CRSSQSLLHSNGYNYLD WYLQKPGQSPQLLIY LGSNRAS GVPDR

FSGSGSGTDFTLKISRVEAEDVGVYYC MQALQ



SEQ ID NO.: 85: candidate human model for 25E9 light chain variable

domain

DIVMTQSPLSLPVTPGEPASISC RSSQSLLHSDGNNYLN WYLQKPGQSPQLLIY LVSNRAS GVPDR

FSGSGSGTDFTLKISRVEAEDVGVYYC MQALQPRXT FGQGTKVEIK



SEQ ID NO.: 86: candidate human model for 25E9 heavy chain variable

domain

QVQLQQSGAEVKKPGSSVKVSCKAS GGTFSTYSIS WVRQAPGHGLEWMG RIFPLLGVAKYAQKFQG

RVTITADKSTSTAYMELSSLRSEDTAVYYCAV PRSSSYWFDP WGQGTLVTVSS 5



SEQ ID NO.: 87: candidate human model for 25E9 heavy chain variable

domain

EVQLVQSGAEVKKPGSSVKVSCKAS GGTFSSYAIS WVRQAPGQGLEWMG GIIPIFGTANYAQKFQG

RVTITADESTSTAYMELSSLRSEDTAVYYCAR GNYDSSGYDDAFDI WGQGTMVTVSS



SEQ ID NO.: 88: candidate human model for 25E9 heavy chain variable

domain

EVQLVQSGAEVKKPGSSVKLSCKAS GDTFSSRPVS WVRQAPGQGLEWMG GIIPIFRTTNYAQKFQG

RVTITADESMTTAYLELRGLTSDDTAVYYCAT TRMKITVFASTFDY WGQGTLVTVSS



SEQ ID NO.: 89: candidate human model for 25E9 heavy chain variable

domain

QVQLVQSGAEVKKPGSSVKVSCKAS GGTFSSYAIS WVRQAPGQGLEWMG GIIPIFGTANYAQKFQG

RVTITADKSTSTAYMELSSLRSEDTAVYYC



SEQ ID NO.: 90: candidate human model for 25E9 heavy chain variable

domain

QVQLVQSGAEVKKPGASVKVSCKAS GYTFTSYYMH WVRQAPGQGLEWMG IINPSGGSTSYAQKFQG

RVTMTRDTSTSTVYMELSSLRSEDTAVYYC



SEQ ID NO.: 91: candidate human model for 25E9 heavy chain variable

domain

EVQLVQSGAEVKKPGATVKISCKVS GYTFTDYYMH WVQQAPGKGLEWMG LVDPEDGETIYAEKFQG

RVTITADTSTDTAYMELSSLRSEDTAVYYCAT



SEQ ID NO.: 92: candidate human model for 25E9 heavy chain variable

domain

QVQLVQSGAEVKKPGASVKVSCKAS GYTFTSYAIS WVRQAPGQGLEWMG WINPGNGDTNYAQKFQG

RVTITADTSTSTAYMELSSLRSEDTAVYYCAR APGYGSRGDYXFDY WGQGTLVTVSS