US20040208876A1 - Monoclonal antibodies to hepatocyte growth factor - Google Patents

Monoclonal antibodies to hepatocyte growth factor Download PDF

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US20040208876A1
US20040208876A1 US10/825,060 US82506004A US2004208876A1 US 20040208876 A1 US20040208876 A1 US 20040208876A1 US 82506004 A US82506004 A US 82506004A US 2004208876 A1 US2004208876 A1 US 2004208876A1
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hgf
mab
mabs
cells
binding
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Kyung Kim
Yi-Chi Su
Lihong Wang
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Galaxy Biotech LLC
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Priority to US10/825,060 priority Critical patent/US20040208876A1/en
Priority to BRPI0418745-8A priority patent/BRPI0418745A/pt
Priority to NZ550324A priority patent/NZ550324A/en
Priority to EP04781281A priority patent/EP1734995B1/de
Priority to AT04781281T priority patent/ATE473760T1/de
Priority to MXPA06011822A priority patent/MXPA06011822A/es
Priority to KR1020067023964A priority patent/KR101072736B1/ko
Priority to JP2007508323A priority patent/JP4594381B2/ja
Priority to US10/917,915 priority patent/US7220410B2/en
Priority to DK04781281.3T priority patent/DK1734995T3/da
Priority to EP10160203A priority patent/EP2204191A1/de
Priority to PCT/US2004/026565 priority patent/WO2005107800A1/en
Priority to CNA200480042750XA priority patent/CN1964738A/zh
Priority to SI200431468T priority patent/SI1734995T1/sl
Priority to RU2006140257/13A priority patent/RU2361879C2/ru
Priority to CA2563080A priority patent/CA2563080C/en
Priority to ES04781281T priority patent/ES2346886T3/es
Priority to DE602004028168T priority patent/DE602004028168D1/de
Priority to PT04781281T priority patent/PT1734995E/pt
Priority to PL04781281T priority patent/PL1734995T3/pl
Priority to AU2004319276A priority patent/AU2004319276C1/en
Priority to ZA200609407A priority patent/ZA200609407B/xx
Publication of US20040208876A1 publication Critical patent/US20040208876A1/en
Assigned to GALAXY BIOTECH, LLC reassignment GALAXY BIOTECH, LLC ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KIM, KYUNG JIN, WANG, LIHONG, SU, YI-CHI
Priority to IL178474A priority patent/IL178474A/en
Priority to CR8698A priority patent/CR8698A/es
Priority to NO20065227A priority patent/NO20065227L/no
Priority to HK07101333.7A priority patent/HK1094167A1/xx
Priority to US11/710,009 priority patent/US7494650B2/en
Priority to US11/818,305 priority patent/US7687063B2/en
Priority to US12/342,059 priority patent/US20090104192A1/en
Assigned to GALAXY BIOTECH, LLC reassignment GALAXY BIOTECH, LLC CORRECTIVE ASSIGNMENT TO CORRECT ASSIGNEE ADDRESS, PREVIOUSLY RECORDED ON REEL 015780 FRAME 0417. ASSIGNORS HEREBY CONFIRMS THE ASSIGNMENT. Assignors: WANG, LIHONG, KIM, KYUNG JIN, SU, YI-CHI
Priority to JP2010174810A priority patent/JP2011012067A/ja
Priority to CY20101100789T priority patent/CY1110783T1/el
Priority to HR20100521T priority patent/HRP20100521T1/hr
Priority to US13/160,444 priority patent/US20120064066A1/en
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/22—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against growth factors ; against growth regulators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
    • C07K2317/92—Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
    • G01N2333/435—Assays involving biological materials from specific organisms or of a specific nature from animals; from humans
    • G01N2333/475—Assays involving growth factors
    • G01N2333/4753—Hepatocyte growth factor; Scatter factor; Tumor cytotoxic factor II

Definitions

  • the present invention relates generally to the combination of monoclonal antibody (mAb) and recombinant DNA technologies for developing novel biologics, and more particularly, for example, to the production of monoclonal antibodies that bind to and neutralize Hepatocyte Growth Factor.
  • mAb monoclonal antibody
  • recombinant DNA technologies for developing novel biologics, and more particularly, for example, to the production of monoclonal antibodies that bind to and neutralize Hepatocyte Growth Factor.
  • HGF Human Hepatocyte Growth Factor
  • HGF pleiotropic activity of HGF are mediated through its receptor, a transmembrane tyrosine kinase encoded by the proto-oncogene cMet.
  • HGF and its receptor c-Met have been shown to be involved in the initiation, invasion and metastasis of tumors (Jeffers et al., J. Mol. Med. 74:505, 1996; Comoglio and Trusolino, J. Clin. Invest. 109:857, 2002).
  • HGF/cMet are coexpressed, often over-expressed, on various human solid tumors including tumors derived from lung, colon, rectum, stomach, kidney, ovary, skin, multiple myeloma and thyroid tissue (Prat et al., Int. J. Cancer 49:323, 1991; Chan et al., Oncogene 2:593, 1988; Weidner et al., Am. J. Respir. Cell. Mol. Biol. 8:229, 1993; Derksen et al., Blood 99:1405, 2002). HGF acts as an autocrine (Rong et al., Proc. Natl. Acad. Sci.
  • antagonistic molecules for example antibodies, blocking the HGF-cMet pathway potentially have wide anti-cancer therapeutic potential.
  • HGF is a 102 kDa protein with sequence and structural similarity to plasminogen and other enzymes of blood coagulation (Nakamura et al., Nature 342:440, 1989; Weidner et al., Am. J. Respir. Cell. Mol. Biol. 8:229, 1993) (FIG. 1). HGF is synthesized as a 728 amino acid precursor (preproHGF), which undergoes intracellular cleavage to an inactive, single chain form (proHGF) (Nakamura et al., Nature 342:440, 1989; Rosen et al., J. Cell. Biol. 127:1783, 1994).
  • preproHGF 728 amino acid precursor
  • proHGF inactive, single chain form
  • proHGF Upon extracellular secretion, proHGF is cleaved to yield the biologically active disulfide-linked heterodimeric molecule composed of an ⁇ -subunit and ⁇ -subunit (Nakamura et al., Nature 342:440, 1989; Naldini et al., EMBO J. 11:4825, 1992).
  • the ⁇ -subunit contains 440 residues (69 kDa with glycosylation), consisting of the N-terminal hairpin domain and four kringle domains.
  • the ⁇ -subunit contains 234 residues (34 kDa) and has a serine protease-like domain, which lacks proteolytic activity.
  • HGF HGF contains 4 putative N-glycosylation sites, 1 in the ⁇ -subunit and 3 in the ⁇ -subunit.
  • NK2 (a protein encompassing the N-terminus and first two kringle domains of the ⁇ -subunit) is sufficient for binding to cMet and activation of the signal cascade for motility, however the full length protein is required for the mitogenic response (Weidner et al., Am. J. Respir. Cell. Mol. Biol. 8:229, 1993).
  • H SPG binds to HGF by interacting with the N terminus of HGF (Aoyama, et al., Biochem. 36:10286, 1997; Sakata, et al., J. Biol. Chem. 272:9457, 1997).
  • H SPG-HGF interaction Postulated roles for the H SPG-HGF interaction include the enhancement of HGF bioavailability, biological activity and oligomerization (Bardelli, et al., J. Biotechnol. 37:109, 1994; Zioncheck et al., J. Biol. Chem. 270:16871, 1995).
  • cMet is a member of the class IV protein tyrosine kinase receptor family.
  • the full length cMet gene was cloned and identified as the cMet proto-oncogene (Cooper et al., Nature 311:29, 1984; Park et al., Proc. Natl. Acad. Sci. USA 84:6379, 1987).
  • the cMet receptor is initially synthesized as a single chain, partially glycosylated precursor, p170 (MET) (FIG. 1) (Park et al., Proc. Natl. Acad. Sci.
  • the protein Upon further glycosylation, the protein is proteolytically cleaved into a heterodimeric 190 kDa mature protein (1385 amino acids), consisting of the 50 kDa ⁇ -subunit (residues 1-307) and the 145 kDa 1-subunit.
  • the cytoplasmic tyrosine kinase domain of the 1-subunit is involved in signal transduction.
  • Antagonistic molecules inhibiting the HGF/cMet interaction are expected to have therapeutic potential as anti-cancer agents since HGF/cMet have been shown to play important roles in several aspects of cancer development such as tumor initiation, invasion, metastasis, regulation of apoptosis and angiogenesis.
  • truncated HGF proteins such as NK1 (N terminal domain plus kringle domain 1; Lokker et al., J. Biol. Chem.
  • NK2 N terminal domain plus kringle domains 1 and 2; Chan et al., Science 254:1382, 1991
  • NK4 N-terminal domain plus four kringle domains; Kuba et al., Cancer Res. 60:6737, 2000
  • anti-cMet mAbs Dodge, Master's Thesis, San Francisco State University, 1998)
  • anti-HGF mAbs Cao et al., Proc. Natl. Acad. Sci. USA 98:7443, 2001.
  • NK1 and NK2 can compete effectively with the binding of HGF to its receptor, but have been shown to have partial agonistic activities in vitro (Cioce et al., J. Biol. Chem. 271:13110, 1996; Schwall et al., J. Cell Biol. 133:709, 1996), rather than purely antagonist activities as desired. More recently, Kuba et al., Cancer Res. 60:6737, 2000, demonstrated that NK4 could partially inhibit the primary growth (FIG. 2) and metastasis of murine lung tumor LLC in a nude mouse model by continuous infusion of NK4. This study further suggests the anti-cancer therapeutic potential of antagonistic molecules of HGF.
  • NK4 had to administered continuously to obtain a partial growth inhibition of primary tumors indicates a potentially short half-life of the NK4 molecule and/or lack of potency.
  • the approach of using antibodies will benefit from their favorable pharmacokinetics and the possibility of obtaining antibodies with much higher potency.
  • the invention provides a neutralizing mAb to human Hepatocyte Growth Factor (HGF).
  • HGF Hepatocyte Growth Factor
  • the mAb inhibits at least one, and preferably several or all biological activities of HGF including binding to its receptor cMet, inducing scattering of cells such as Madin-Darby canine kidney cells, inducing proliferation of 4 MBr-5 monkey epithelial cells and/or hepatocytes and/or HUVEC, and inducing angiogenesis.
  • the Anti-HGF mAb can inhibit such an activity when used as a single agent.
  • a preferred anti-HGF mAb inhibits growth of a human tumor xenograft in a mouse.
  • the mAb of the invention is chimeric, humanized or human.
  • Exemplary antibodies are L2G7 and its chimeric and humanized forms. Cell lines producing such antibodies are also provided.
  • a pharmaceutical composition comprising a neutralizing anti-HGF antibody, e.g., chimeric or humanized L2G7, is provided.
  • the pharmaceutical composition is administered to a patient to treat cancer or other disease.
  • FIG. 1 Schematic models of HGF and cMet.
  • FIG. 2 Graph showing that NK4 partially inhibits the primary growth of murine lung tumor LLC in nude mice (from Kuba et al., Cancer Res. 60:6737, 2000). NK4 was infused continuously for 14 days from 4 th day after tumor implantation s.c. in nude mice.
  • FIG. 3 Graph showing that a cocktail of three anti-HGF mAbs is required to inhibit the growth of human brain tumor U-118 cells in nude mice (from Cao et al., Proc. Natl. Acad. Sci. USA 98:7443, 2001).
  • U-118 tumor cells were injected s.c. into nude mice. From day 1 anti-HGF mAbs A-1, -5, and -7, or mAbs 7-2 and -3 were administered at 200 ⁇ g/injection, twice/wk for 10 wks.
  • FIG. 4 Determination of relative binding epitopes of mAbs L1H4, L2C7, L2G7 using competitive binding ELISA. Plates were coated with recombinant HGF (rHGF), blocked with skim milk and incubated with suboptimal concentration of biotinylated mAbs in the presence of 100 ⁇ excess amounts of unlabeled mAbs. Biotinylated mAb bound was detected by the addition of HRP-Strepavidin.
  • rHGF recombinant HGF
  • FIG. 5 Binding of a nti-HGF mAbs to rHGF as determined in a direct HGF binding ELISA. Plate was coated with the H1-F11 supernatant containing rHGF, blocked by 2% skim milk and incubated with mAbs, followed by the addition of HRP-G ⁇ MIgG (as described under Examples).
  • FIG. 6 Abilities of anti-HGF mAbs to capture rHGF-Flag in solution. Anti-HGF mAbs were captured on a goat anti-mouse IgG coated ELISA plate. Plates were then blocked with 2% skim milk and incubated with rHGF-Flag, followed by HRP-M2 anti-Flag mAb (as described under Examples).
  • FIG. 7 Inhibition of rHGF-Flag binding to cMet-Fc by anti-HGF mAbs in a capture ELISA. cMet-Fc captured on goat anti-human IgG coated plate is incubated with HGF-Flag preincubated with/without mAbs. The bound rHGF-Flag was detected by the addition of HRP-M2 anti-Flag mAb (as described under Examples).
  • FIG. 8 Neutralization of HGF induced MDCK scattering by anti-HGF mAb L2G7.
  • A Control without any treatment.
  • B rHGF+IgG.
  • C rHGF+mAb L2G7.
  • MDCK cells were incubated with a 1:20 dilution of H1-F11 culture supernatant ( ⁇ 3 ⁇ g/ml of HGF) in the presence of 10 ⁇ g/ml of mAbs. Photos were taken at 100 ⁇ magnification.
  • FIG. 9 Inhibition of HGF-induced proliferation of Mv 1 LU cells by L2G7 mAb.
  • the fold molar excess of mAb over HGF is shown on the horizontal axis, and the cpm ⁇ 10 ⁇ 2 incorporated is shown on the vertical axis. Data points were obtained in triplicate.
  • FIG. 10 Inhibition of HGF-induced proliferation of HUVEC by L2G7 mAb and control mouse antibody (IgG). Data points were obtained in triplicate.
  • FIG. 11 Effect on HGF-induced proliferation of HCT 116 colon tumor cells by L2G7 and L1H4 antibodies. Data points were obtained in triplicate.
  • A Tumor size vs day from tumor implantation.
  • B Tumor mass at end of experiment.
  • the invention provides neutralizing anti-HGF monoclonal antibodies, pharmaceutical compositions comprising them, and methods of using them for the treatment of disease.
  • Antibodies are very large, complex molecules (molecular weight of ⁇ 150,000 or about 1320 amino acids) with intricate internal structure.
  • a natural antibody molecule contains two identical pairs of polypeptide chains, each pair having one light chain and one heavy chain.
  • Each light chain and heavy chain in turn consists of two regions: a variable (“V”) region involved in binding the target antigen, and a constant (“C”) region that interacts with other components of the immune system.
  • the light and heavy chain variable regions fold up together in 3-dimensional space to form a variable region that binds the antigen (for example, a receptor on the surface of a cell).
  • Within each light or heavy chain variable region there are three short segments (averaging 10 amino acids in length) called the complementarity determining regions (“CDRs”).
  • the six CDRs in an antibody variable domain fold up together in 3-D space to form the actual antibody binding site which locks onto the target antigen.
  • the position and length of the CDRs have been precisely defined. Kabat, E. et al., Sequences of Proteins of Immunological Interest, U.S. Department of Health and Human Services, 1983, 1987.
  • the part of a variable region not contained in the CDRs is called the framework, which forms the environment for the CDRs.
  • a humanized antibody is a genetically engineered antibody in which the CDRs from a mouse antibody (“donor antibody”, which can also be rat, hamster or other similar species) are grafted onto a human antibody (“acceptor antibody”).
  • donor antibody which can also be rat, hamster or other similar species
  • acceptor antibody is an antibody having CDRs from a donor antibody and variable region framework and constant regions from a human antibody.
  • at least one of two additional structural elements can be employed. See, U.S. Pat. No. 5,530,101 and 5,585,089, incorporated herein by reference, which provide detailed instructions for construction of humanized antibodies.
  • the framework of the heavy chain variable region of the humanized antibody is chosen to have maximal sequence identity (between 65% and 95%) with the framework of the heavy chain variable region of the donor antibody, by suitably selecting the acceptor antibody from among the many known human antibodies.
  • selected amino acids in the framework of the human acceptor antibody are replaced with corresponding amino acids from the donor antibody, in accordance with specified rules.
  • the amino acids to be replaced in the framework are chosen on the basis of their ability to interact with the CDRs.
  • the replaced amino acids can be adjacent to a CDR in the donor antibody sequence or within 4-6 angstroms of a CDR in the humanized antibody as measured in 3-dimensional space.
  • a chimeric antibody is an antibody in which the variable region of a mouse (or other rodent) antibody is combined with the constant region of a human antibody; their construction by means of genetic engineering is well-known. Such antibodies retain the binding specificity of the mouse antibody, while being about two-thirds human. The proportion of nonhuman sequence present in mouse, chimeric and humanized antibodies suggests that the immunogenicity of chimeric antibodies is intermediate between mouse and humanized antibodies.
  • mice Other types of genetically engineered antibodies that may have reduced immunogenicity relative to mouse antibodies include human antibodies made using phage display methods (Dower et al., WO91/17271; McCafferty et al., WO92/001047; and Winter, WO92/20791) or using transgenic animals (Lonberg et al., WO93/12227; Kucherlapati WO91/10741).
  • the epitope of a mAb is the region of its antigen to which the mAb binds.
  • Two antibodies bind to the same or overlapping epitope if each competitively inhibits (blocks) binding of the other to the antigen. That is, a 1 ⁇ , 5 ⁇ , 10 ⁇ , 20 ⁇ or 100 ⁇ excess of one antibody inhibits binding of the other by at least 50% but preferably 75%, 90% or even 99% as measured in a competitive binding assay (see, e.g., Junghans et al., Cancer Res. 50:1495, 1990).
  • two antibodies have the same epitope if essentially all amino acid mutations in the antigen that reduce or eliminate binding of one antibody reduce or eliminate binding of the other.
  • Two antibodies have overlapping epitopes if some amino acid mutations that reduce or eliminate binding of one antibody reduce or eliminate binding of the other.
  • a monoclonal antibody (mAb) that binds HGF i.e., an anti-HGF mAb
  • HGF binds HGF
  • an anti-HGF mAb is said to neutralize HGF, or be neutralizing, if the binding partially or completely inhibits one or more biological activities of HGF (i.e., when the mAb is used as a single agent).
  • HGF human vascular endothelial cell
  • CAM chick embryo chorioallantoic membrane
  • a neutralizing mAb of the invention at a concentration of, e.g., 0.01, 0.1, 0.5, 1, 2, 5, 10, 20 or 50 ⁇ g/ml will inhibit a biological function of HGF by about at least 50% but preferably 75%, more preferably by 90% or 95% or even 99%, and most preferably approximately 100% (essentially completely) as assayed by methods described under Examples or known in the art.
  • the extent of inhibition is measured when the amount of HGF used is just sufficient to fully stimulate the biological activity, or is 0.05, 0.1, 0.5, 1, 3 or 10 ⁇ g/ml.
  • the mAb will be neutralizing, i.e., inhibit the biological activity, when used as a single agent, but possibly 2 mAbs will be needed together to give inhibition.
  • the mAb will neutralize not just one but two, three or several of the biological activities listed above; for purposes herein, an anti-HGF mAb that used as a single agent neutralizes all the biological activities of HGF will be called “fully neutralizing”, and such mAbs are most preferable.
  • MAbs of the invention will preferably be specific for HGF, that is they will not bind, or only bind to a much lesser extent, proteins that are related to HGF such as fibroblast growth factor (FGF) and vascular endothelial growth factor (VEGF).
  • FGF fibroblast growth factor
  • VEGF vascular endothelial growth factor
  • MAbs of the invention will typically have a binding affinity (K a ) for HGF of at least 10 7 M ⁇ 1 but preferably 10 8 M ⁇ 1 or higher, and most preferably 10 9 M ⁇ 1 or higher or even 10 10 M ⁇ 1 or higher.
  • MAbs of the invention include anti-HGF antibodies in their natural tetrameric form (2 light chains and 2 heavy chains) and may be of any of the known isotypes IgG, IgA, IgM, IgD and IgE and their subtypes, i.e., human IgG1, IgG2, IgG3, IgG4 and mouse IgG1, IgG2a, IgG2b, and IgG3.
  • the mAbs of the invention are also meant to include fragments of antibodies such as Fv, Fab and F(ab′) 2 ; bifunctional hybrid antibodies (e.g., Lanzavecchia et al., Eur. J. Immunol.
  • the mAbs may be of animal (e.g., mouse, rat, hamster or chicken) origin, or they may be genetically engineered.
  • Rodent mAbs are made by standard methods well-known in the art, comprising multiple immunization with HGF in appropriate adjuvant i.p., i.v., or into the footpad, followed by extraction of spleen or lymph node cells and fusion with a suitable immortalized cell line, and then selection for hybridomas that produce antibody binding to HGF, e.g., see under Examples.
  • Chimeric and humanized mAbs made by art-known methods mentioned supra, are preferred embodiments of the invention.
  • Human antibodies made, e.g., by phage display or transgenic mice methods are also preferred (see e.g., Dower et al., McCafferty et al., Winter, Lonberg et al., Kucherlapati, supra).
  • the neutralizing anti-HGF mAbs L1H4, L2C7 and L2G7 mAbs described infra are examples of the invention, with L2G7 a preferred example.
  • Neutralizing mAbs with the same or overlapping epitope as any of these mAbs, e.g., as L2G7, provide other examples.
  • a chimeric or humanized form of L2G7 is an especially preferred embodiment.
  • MAbs that are 90%, 95% or 99% identical to L2G7 in amino acid sequence and maintain its functional properties, or which differ from it by a small number of functionally inconsequential amino acid substitutions (e.g., conservative substitutions), deletions, or insertions are also included in the invention.
  • Native mAbs of the invention may be produced from their hybridomas.
  • Genetically engineered mAbs e.g., chimeric or humanized mAbs, may be expressed by a variety of art-known methods. For example, genes encoding their light and heavy chain V regions may be synthesized from overlapping oligonucleotides and inserted together with available C regions into expression vectors (e.g., commercially available from Invitrogen) that provide the necessary regulatory regions, e.g., promoters, enhancers, poly A sites, etc. Use of the CMV promoter-enhancer is preferred.
  • the expression vectors may then be transfected using various well-known methods such as lipofection or electroporation into a variety of mammalian cell lines such as CHO or non-producing myelomas including Sp2/0 and NSO, and cells expressing the antibodies selected by appropriate antibiotic selection. See, e.g., U.S. Pat. No. 5,530,101. Larger amounts of antibody may be produced by growing the cells in commercially available bioreactors.
  • the mAbs or other antibodies of the invention may be purified according to standard procedures of the art such as microfiltration, ultrafiltration, protein A or G affinity chromatography, size exclusion chromatography, anion exchange chromatography, cation exchange chromatography and/or other forms of affinity chromatography based on organic dyes or the like.
  • Substantially pure antibodies of at least about 90 or 95% homogeneity are preferred, and 98% or 99% or more homogeneity most preferred, for pharmaceutical uses.
  • the present invention provides a pharmaceutical formulation comprising the antibodies described herein.
  • Pharmaceutical formulations of the antibodies contain the mAb in a physiologically acceptable carrier, optionally with excipients or stabilizers, in the form of lyophilized or aqueous solutions.
  • Acceptable carriers, excipients or stabilizers are nontoxic to recipients at the dosages and concentrations employed, and include buffers such as phosphate, citrate, or acetate at a pH typically of 5.0 to 8.0, most often 6.0 to 7.0; salts such as sodium chloride, potassium chloride, etc.
  • the mAb is typically present at a concentration of 1-100 mg/ml, e.g., 10 mg/ml.
  • the invention provides a method of treating a patient with a disease using an anti-HGF mAb in a pharmaceutical formulation.
  • the mAb prepared in a pharmaceutical formulation can be administered to a patient by any suitable route, especially parentally by intravenous infusion or bolus injection, intramuscularly or subcutaneously. Intravenous infusion can be given over as little as 15 minutes, but more often for 30 minutes, or over 1, 2 or even 3 hours.
  • the mAb can also be injected directly into the site of disease (e.g., a tumor), or encapsulated into carrying agents such as liposomes.
  • the dose given will be sufficient to alleviate the condition being treated (“therapeutically effective dose”) and is likely to be 0.1 to 5 mg/kg body weight, for example 1, 2, 3 or 4 mg/kg, but may be as high as 10 mg/kg or even 15 or 20 mg/kg.
  • a fixed unit dose may also be given, for example, 50, 100, 200, 500 or 1000 mg, orthe dose may be based on the patient's surface area, e.g., 100 mg/m 2 .
  • 1 and 8 doses e.g., 1, 2, 3, 4, 5, 6, 7 or 8
  • the mAb can be administered daily, biweekly, weekly, every other week, monthly or at some other interval, depending, e.g. on the half-life of the mAb, for 1 week, 2 weeks, 4 weeks, 8 weeks, 3-6 months or longer. Repeated courses of treatment are also possible, as is chronic administration.
  • Diseases especially susceptible to therapy with the anti-HGF mAbs of this invention include solid tumors believed to require angiogenesis or to be associated with elevated levels of HGF, for example ovarian cancer, breast cancer, lung cancer (small cell or non-small cell), colon cancer, prostate cancer, pancreatic cancer, gastric cancer, liver cancer, head-and-neck tumors, melanoma, sarcomas, and brain tumors (e.g., glioblastomas). Leukemias and lymphomas may also be susceptible.
  • the anti-HGF mAb will be administered together with (i.e., before, during or after) other anti-cancer therapy.
  • the anti-HGF mAb may be administered together with any one or more of the chemotherapeutic drugs known to those of skill in the art of oncology, for example Taxol (paclitaxel) or its derivatives, platinum compounds such as carboplatin or cisplatin, anthrocyclines such as doxorubicin, alkylating agents such as cyclophosphamide, anti-metabolites such as 5-fluorouracil, or etoposide.
  • the anti-HGF mAb can be administered in combination with two, three or more of these agents in a standard chemotherapeutic regimen, for example taxol and carboplatin, e.g. for breast and ovarian cancer.
  • agents with which the anti-HGF mAb can be administered include biologics such as monoclonal antibodies, including HerceptinTM against the HER2 antigen, AvastinTM against VEGF, or antibodies to the EGF receptor, as well as small molecule anti-angiogenic drugs.
  • biologics such as monoclonal antibodies, including HerceptinTM against the HER2 antigen, AvastinTM against VEGF, or antibodies to the EGF receptor, as well as small molecule anti-angiogenic drugs.
  • the anti-HGF mAb can be used together with radiation therapy or surgery.
  • Treatment including the anti-HGF mAb antibody may increase the median progression-free survival or overall survival time of patients with these tumors (e.g., ovarian, breast, lung, colon and glioblastomas, especially when relapsed or refractory) by at least 30% or 40% but preferably 50%, 60% to 70% or even 100% or longer, compared to the same treatment (e.g., chemotherapy) but without anti-HGF mAb.
  • tumors e.g., ovarian, breast, lung, colon and glioblastomas, especially when relapsed or refractory
  • treatment including the anti-HGF mAb may increase the complete response rate, partial response rate, or objective response rate (complete+partial) of patients with these tumors (e.g., ovarian, breast, lung, colon and glioblastomas especially when relapsed or refractory) by at least 30% or 40% but preferably 50%, 60% to 70% or even 100% compared to the same treatment (e.g., chemotherapy) but without the anti-HGF mAb.
  • tumors e.g., ovarian, breast, lung, colon and glioblastomas especially when relapsed or refractory
  • the anti-HGF mAbs of the invention also find use in diagnostic, prognostic and laboratory methods. They may be used to measure the level of HGF in a tumor or in the circulation of a patient with a tumor, and therefore to follow and guide treatment of the tumor. For example, a tumor associated with high levels of HGF would be especially susceptible to treatment with an anti-HGF mAb.
  • the mAbs can be used in an ELISA or radioimmunoassay to measure the level of HGF, e.g., in a tumor biopsy specimen or in serum or in media supernatant of HGF-secreting cells in cell culture.
  • the use of two anti-HGF mAbs binding to different epitopes will be especially useful in developing a sensitive “sandwich” ELISA to detect HGF.
  • the mAb may be labeled with fluorescent molecules, spin-labeled molecules, enzymes or radioisotypes, and may be provided in the form of kit with all the necessary reagents to perform the assay for HGF.
  • the anti-HGF mAbs will be used to purify HGF, e.g., by affinity chromatography.
  • recombinant human HGF was first produced in a mammalian expression system.
  • cDNAs encoding the recombinant human HGF (rHGF) or rHGF-Flag peptide (8 amino acid residues of Flag attached to the c-terminus of HGF) were constructed in a pIND-inducible expression vector (No et al., Proc. Natl. Acad. Sci. USA. 93:3346, 1996). These cDNAs were then transfected into EcR-293 human kidney fibroblast cells (Invitrogen) using Fugene transfection reagent (Roche).
  • H1-F11 and 24.1, secreting HGF and HGF-Flag respectively were selected in the presence of 600 ⁇ g/ml of G418 and 400 ⁇ g/ml of Zeocin (Invitrogen).
  • H1-F11 and 24.1 were induced to secrete HGF and HGF-Flag by treatment with 4 ⁇ M of Ponasterone A (Invitrogen) for 4-5 days in serum free DMEM containing glutamine and antibiotics.
  • HGF secreted into the culture supernatant was concentrated approximately 100-fold using a membrane ultrafiltration cartridge with an MW 50,000 cut-off filter [amicon Centriprep YM-50 filter followed by microcon YM-50 filter (Millipore)].
  • a membrane ultrafiltration cartridge with an MW 50,000 cut-off filter [amicon Centriprep YM-50 filter followed by microcon YM-50 filter (Millipore)].
  • Such concentrated H1F11 culture supernatant contains ⁇ 100 ⁇ g/ml of HGF and ⁇ 120 ⁇ g/ml of bovine serum albumin.
  • mice were immunized in each hind foot pad >10 times at one week intervals, with 1-2 ⁇ g of purified rHGF (Pepro Tech) or 1-2 ⁇ g of rHGF plus 1-2 ⁇ g of BSA (concentrated H1-F11 culture supernatant) resuspended in MPL-TDM (Ribi Immunochem. Research).
  • PMP purified rHGF
  • BSA concentrated H1-F11 culture supernatant
  • popliteal lymph node cells were fused with murine myeloma cells, P3X63AgU.1 (ATCC CRL1597), using 35% polyethylene glycol.
  • Hybridomas were selected in HAT medium as described (Chuntharapai and Kim, J. Immunol. 163:766, 1997).
  • hybridoma culture supernatants were screened in a direct HGF binding ELISA as well as in an HGF-Flag capture ELISA.
  • the latter assay was used to further confirm the specificity of anti-HGF mAbs selected using the direct HGF binding ELISA and to select mAbs that can bind to HGF in solution phase. Blocking activities of selected mAbs were then determined in the HGF-Flag/cMet-Fc binding ELISA and in the MDCK scatter assay as described (Jeffers et al., Proc. Natl. Acad. Sci. USA 95:14417, 1998). Selected hybridomas were cloned twice using limiting dilution techniques.
  • the isotype of mAbs were determined using an isotyping kit (Zymed). Ascites of selected mAbs were raised and purified using ImmunoPure (A/G) IgG Purification Kit (Pierce). Also biotinylated mAbs were prepared using EZ-sulfo-NHS-LC-Biotin according to the instructions provided by Pierce. Each of the assays referred to here is described in more detail below.
  • microtiter plates (Maxisorb; Nunc) are coated with 50 ⁇ l/well of H1-F11 culture supernatants containing rHGF, diluted in PBS at a 1:2 ratio of HGF/PBS, overnight at 4° C.
  • HGF-Flag capture ELISA microtiter plates are coated with 50 ⁇ l/well of 2 ⁇ g/ml of goat antibodies specific to the Fc portion of mouse IgG (G ⁇ MIgG-Fc) in PBS overnight at 4° C. and blocked with 2% skim milk for 1 hr at RT. After washing, the plates are incubated with 50 ⁇ l/well of purified mAbs or hybridoma culture supernatants for 1 hr. After washing, plates are then incubated with 50 ⁇ l/well of 24.1 cell culture supernatant containing rHGF-Flag.
  • HRP-M2 anti-Flag mAb Invitrogen
  • plates are then incubated with 50 ⁇ l/well of HRP-M2 anti-Flag mAb (Invitrogen) in the presence of 15 ⁇ g/ml of murine IgG.
  • the bound HRP-anti-Flag M2 is detected by the addition of the substrate as described above. Washes are carried out 3 times in wash buffer.
  • At least three mAbs obtained from hybridomas generated by immunizing the Balb/c mice with rHGF in concentrated H1-F11 culture supernatant as described above, showed binding in both the direct rHGF binding ELISA and the HGF-Flag capture ELISA and were selected for further study. These hybridomas were then cloned twice, ascites were raised in mice by standard methods, and mAbs were purified using a protein G/A column. Their isotypes were determined using an isotyping kit (Zymed Lab). The L2G7 hybridoma has been deposited with the American Type Culture Collection (ATCC Number PTA-5162) under the Budapest Treaty.
  • the binding epitopes of the antibodies were partially characterized by a competitive binding ELISA in which a 100 ⁇ excess of unlabeled mAb was used to compete with the binding of the same or another biotinylated mAb in the HGF binding ELISA.
  • FIG. 4 shows that the binding of the anti-HGF mAbs, L1H4 and L2G7, was inhibited only by themselves, suggesting that they recognize unique epitopes.
  • the binding of L2C7 was inhibited by L2G7 but not by L1H4. This suggests that the L2C7 epitope overlaps with that of L2G7 but not of L1H4.
  • L2C7 was not able to inhibit the binding of L2G7, suggesting that the L2C7 and L2G7 epitopes overlap but are distinct, and/or the affinity of L2C7 is much lower than that of L2G7.
  • the epitopes of L1H4, L2C7 and L2G7 are respectively designated A, B and C.
  • the relative binding abilities of the three anti-HGF mAbs were measured using purified antibodies in the direct HGF binding ELISA, in which rHGF is first bound to the plate. In this assay, L2C7 and L2G7 bound better than L1H4 (FIG. 5). The ability of the mAbs to bind rHGF-Flag in solution was also determined, using the HGF-Flag capture ELISA. All three mAbs were able to capture rHGF-Flag in solution phase but mAb L2G7 was more effective than the others (FIG. 6). These results suggest that mAb L2G7 has the highest binding affinity to HGF among the three mAbs.
  • HGF histoneum kinase kinase kinase
  • cMet-Fc was first produced by transfecting human fibroblast 293 cells with cDNA encoding residues 1-929 ECD of cMet linked with the Fc portion of human IgG1 (residues 216 to 446) as described by Mark et al., J. Biol. Chem. 267:26166, 1992 in the pDisplay expression vector (Invitrogen).
  • Microtiter plates are coated with 50 ⁇ l/well of 2 ⁇ g/ml of goat antibodies specific to the Fc portion of human IgG (G ⁇ HIgG-Fc) in PBS overnight at 4° C. and blocked with 2% BSA for 1 hr at RT. After washing the plates, 50 ⁇ l of culture supernatant of 293 transfected with cMet-Fc cDNA is added to each well for 1 hr at RT. After washing the plates, 50 ⁇ l/well of 24.1 cell culture supernatant containing rHGF-Flag, preincubated with various concentrations of mAbs, is added to each well for 1 hr.
  • HRP-M2 anti-Flag mAb Invitrogen
  • the bound HRP-anti-Flag M2 is detected by the addition of the substrate as described above. Washes are carried out 3 times in wash buffer.
  • the receptor protein used in cMet-Fc/HGF-Flag binding ELISA is a soluble receptor protein, its conformation may be different from that of the natural membrane bound receptor.
  • HGF binds to HSPG in addition to cMet and it is known that the HSPG-HGF interaction enhances various HGF activities.
  • mAbs blocking the interaction of HGF with soluble cMet may not necessarily have the capacity to neutralize HGF bioactivities on the cells. Thus, it is important to further confirm the blocking activities of mAbs in selected biological systems.
  • HGF is known to be a potent scattering factor.
  • the neutralizing activity of the anti-HGF mAbs was also determined using the Madin-Darby canine kidney (MDCK cells obtained from ATCC) scatter assay as described (Jeffers et al., Proc. Natl. Acad. Sci. USA 95:14417, 1998). MDCK cells grown in DMEM supplemented with 5% FCS are plated at 10 3 cells/100 ⁇ l/well in the presence of predetermined concentrations of rHGF with or without mAbs in DMEM with 5% FCS. After 2 days incubation at 37° C. in 5% CO 2 , cells are then washed in PBS, fixed in 2% formaldehyde for 10 m in at RT. After washing in PBS cells are stained with 0.5% crystal violet in 50% ethanol (v/v) for 10 min at RT. Scattering activity is determined by microscopic examination.
  • HGF is a member of the heparin binding growth factor family including fibroblast growth factor (FGF) and vascular endothelial growth factor (VEGF). Also, HGF has ⁇ 40% overall sequence similarity with plasminogen (Nakamura et al., Nature. 342:440, 1989) and shares a similar domain structure with macrophage stimulating protein (MSF, Wang et al., Scand. J. Immunol. 56:545, 2002). Thus, the binding specificity of the anti-HGF antibodies must be determined. The binding of anti-HGF mAbs to these HGF related proteins (available from R&D systems) is assayed using a direct binding ELISA similar to the one for HGF described above. MAb L2G7, mAb L2C7 and mAb L1H4 will not significantly bind to these proteins, demonstrating their specificity for HGF.
  • FGF fibroblast growth factor
  • VEGF vascular endothelial growth factor
  • HGF has a number of biological activities that make it likely that it plays a role in the growth and invasiveness of certain human tumors.
  • One such activity of HGF is as a powerful mitogen for hepatocytes and other epithelial cells (Rubin et al., Proc. Natl. Acad. Sci. USA. 88:415, 1991).
  • the effects of the mAbs on the HGF-induced proliferation of 4 MBr-5 monkey epithelial cells (ATCC) or rat hepatocytes are determined.
  • Hepatocytes are isolated according to a method described by Garrison and Haynes, J. Biol. Chem. 269:4264, 1985.
  • C ells are resuspended at 5 ⁇ 1 04 cells/ml in DMEM containing 5% FCS and stimulated with a predetermined concentration of HGF with various concentration of mAbs. After 21 ⁇ 2 days incubation at 37° C. in 5% CO 2 , the level of cell proliferation is determined by the addition of 3 H-thymidine for 4 hrs. Cells are harvested using an automated cell harvester and the level of 3 H-thymidine incorporated is determined on a scintillation counter. At sufficient concentrations, mAb L2G7 may largely or completely inhibit HGF-induced proliferation of the cells, and mAbs L2C7 and L1H4 may at least partially inhibit proliferation. These antibodies may also inhibit the HGF-induced proliferation of other cell lines.
  • the inhibitory activity of L2G7 on the HGF-induced proliferation of mink lung Mv 1 Lu cells was determined (Borset et al., J. Immunol. Methods 189:59, 1996).
  • Cells grown in DMEM containing 10% FCS are harvested by treatment with EDTA/trysin. After washing, the cells are resuspended at 5 ⁇ 10 4 cells/ml in serum free DMEM with a predetermined concentration (50 ng/ml) of HGF +/ ⁇ various concentrations of mAb. After 1 day incubation at 37° C. in 5% CO 2 , the level of cell proliferation is determined by the addition of 1 ⁇ Ci of 3 H-thymidine for an additional 24 hr.
  • FIG. 9 shows that the addition of 100-fold higher molar concentration of L2G7 mAb completely inhibited the proliferative response of Mv 1 Lu cells. Indeed, L2G7 even at a 3-fold molar ratio of mAb to HGF showed complete inhibition, while control IgG showed no inhibition even at 100-fold molar excess.
  • HGF is also reported to be a potent angiogenesis factor (Bussolino et al., J. Cell Biol. 119:629, 1992; Cherrington et al., Adv. Cancer Res. 79:1, 2000), and angiogenesis, the formation of new blood vessels, is believed to be essential to the growth of tumors. Therefore, the ability of the anti-HGF mAbs to inhibit the angiogenic properties of HGF is shown in three assays: (i) proliferation of human vascular endothelial cells (HUVEC), (ii) tube formation of HUVEC, and (iii) development of new blood vessels on the chick embryo chorioallantoic membrane (CAM). Since HGF has been shown to synergize with VEGF in angiogenesis (Xin et al., Am. J. Pathol. 158:1111, 2001), these assays may be performed both in the presence and absence of VEGF.
  • HUVEC human vascular endothelial cells
  • CAM
  • HUVEC proliferation assay is performed as described with a modification (Conn et al., Proc. Natl. Acad. Sci. USA 87:1323, 1990).
  • HUVEC cells obtained from Clonetics are grown in Endothelial Growth Medium (EBM-2) containing 10% FCS plus endothelial cell growth supplements provided by Clonetics.
  • EBM-2 Endothelial Growth Medium
  • FCS endothelial cell growth supplements
  • FCS endothelial cell growth supplements provided by Clonetics.
  • FCS endothelial cell growth supplements
  • the cells are resuspended to be 10 5 cells/ml in medium-199 containing antibiotics, 10 mM HEPES and 10% FCS (assay medium).
  • HUVEC cells 50 ⁇ l/well are added to microtiter wells containing a suitable concentration of HGF with various concentrations of anti-HGF mAbs for 1 hr at 37° C. After cells are incubated for 72 hr at 37° C. in 5% CO 2 , the level of cell proliferation is determined by incorporation of 3 H-thymidine for 4 hrs. At sufficient concentrations, mAb L2G7 will largely or completely inhibit HGF-induced proliferation of the HUVEC, and mAbs L2C7 and L1H4 may at least partially inhibit proliferation.
  • the level of cell proliferation may be determined by the well-known colorimetric MTT assay.
  • the HUVECs (10 4 cells/100 ⁇ l/well) are grown in serum free medium for 24 hr, and then incubated with 100 ⁇ l of 50 ng/ml of HGF (predetermined to be a suboptimal amount) with various concentrations of mAb L2G7 for 72 hr.
  • MTT solution (5 mg/ml) is added to each well (20 ⁇ l/200 ⁇ l medium) for 4 hr. Then 100 ⁇ l medium/well is removed and mixed with 100 ⁇ l/well of acidified isopropyl alcohol (0.04N HCl in isopropyl).
  • the plates are read on an ELISA reader at 560 nm.
  • the % maximum response is calculated as follows: [OD of HGF+mAB treated cells ⁇ OD of untreated cells]/[OD of HGF treated cells ⁇ OD of untreated cells] ⁇ 100.
  • FIG. 10 shows that even a 4-fold molar excess of L2G7 mAB largely blocks the proliferation of HUVEC in response to HGF.
  • HUVEC Clonetics
  • EGM EGM medium supplemented with 10% FBS
  • endothelial cell growth supplements EGM medium supplemented with 10% FBS
  • Endothelial cell growth supplements EGM medium supplemented with 10% FBS
  • Plates are coated with Matrigel (BD Biosciences) according to the manufacture's instructions at 37° C. for 30 min, and the cells are seeded as 3 ⁇ 10 6 cells/ml in 1 ⁇ basal medium with HGF and various concentrations of anti-HGF mAbs.
  • Tube formation is evaluated under microscope at low-power (10 ⁇ ) magnification. At sufficient concentrations, mAb L2G7 will largely or completely inhibit HGF-induced endothelial tube formation, and mAbs L2C7 and L1H4 may at least partially inhibit it.
  • the chick embryo chorioallantoic membrane (CAM) assay is performed essentially as described (Kim et al, Nature 362:841, 1993). Three-day old chicken embryos are removed from their shells and grown in petri dishes in 5% CO 2 at 37° C. Seven days later, dried methylcellulose discs containing HGF with various concentrations of anti-HGF mAbs are layered onto the CAM. The methylcellulose discs are prepared by mixing 5 ⁇ l of 1.5% methylcellulose in PBS with 5 ⁇ l of HGF preincubated with mAbs. Three days later the development of blood vessels around methylcellulose discs are examined. At sufficient concentrations, mAb L2G7 will largely or completely inhibit such blood vessel formation, and mAbs L2C7 and L1H4 may at least partially inhibit it.
  • CAM chick embryo chorioallantoic membrane
  • HGF is also reported to promote tumor growth (Comoglio and Trusolino, J. Clin. Invest. 109:857, 2002).
  • the ability of the anti-HGF antibodies to inhibit this activity is shown in two steps. First, a number of tumor cell lines are examined for their ability to secrete HGF and proliferate in response to HGF since HGF may be an autocrine growth factor for some of these cells. These cell lines include a panel of human tumor cell lines known to express HGF and cMet (Koochekpour et al., Cancer Res. 57:5391, 1997; Wang et al., J. Cell Biol. 153:1023, 2001).
  • Specific cell lines to be tested include U-118 glioma, HCT116 colon carcinoma, A549 lung carcinoma and A431 epidermoid carcinoma cells, all available from the ATCC. Once such tumor cell lines are identified, the effect of anti-HGF mAbs on the proliferative response to HGF of these cells is determined, using methods similar to those described above. At sufficient concentrations, mAb L2G7 will largely or completely inhibit HGF-induced proliferation of many or all of these cell lines, and mAbs L2C7 and L1H4 may at least partially inhibit proliferation.
  • human HCT116 tumor cells are seeded into 96-well microtiter plates at 5 ⁇ 10 3 cells/well in 200 ⁇ l of DMEM plus 5% FCS. After 24 hr incubation at 37° C. in 5% CO 2 , cells are washed with PBS and incubated in serum free DMEM for 48 hrs. Cells are then incubated with 100 ng/ml of HGF+/ ⁇ 20 ⁇ g/ml of mAbs in DMEM for another 20 hr. As controls, cells grown in DMEM alone or DMEM plus 10% FCS are included. At the end of the incubation, levels of cell proliferation are determined by incorporation of 3 H-thymidine for 4 hr. The result of such an experiment was carried out in triplicates is shown in FIG. 11. HGF induced a moderate proliferation of the HCT116 cells, which was completely abolished by addition of L2G7 antibody (but not by the less potent L1H4 antibody).
  • each anti-HGF antibody will neutralize or inhibit activity when used alone, i.e., as a single agent, but additive or synergistic effects may be achieved by administering the antibody in conjunction with other anti-HGF antibodies or other active agents.
  • mice [0064] The ability of the anti-HGF antibodies to inhibit human tumor growth is demonstrated in xenograft nude mouse models. Experiments are carried out as described previously (Kim et al., Nature 362:841, 1993). Human tumor cells grown in complete DMEM medium are harvested in HBSS. Female athymic nude mice (4-6 wks old) are injected s.c. with typically 5 ⁇ 10 6 cells in 0.1 to 0.2 ml of HBSS in the dorsal areas. When the tumor size reaches 50-100 mm 3 , the mice are grouped randomly and appropriate amounts of the anti-HGF and control mAbs (typically between 0.1 and 1.0 mg, e.g. 0.5 mg) are administered i.p.
  • the number of mice in each treatment group is at least 3, but more often between 5 and 10, e.g., 7.
  • Statistical analysis may be performed using, e.g., Student's t test. In a variation of this experiment, administration of the antibody begins simultaneously or shortly after injection of the tumor cells.
  • the effect of the antibody may also be measured by prolongation of the survival of the mice, or increase in percent of the mice surviving.
  • Various tumor cell lines known to secrete or respond to HGF are used in separate experiments, for example U118 human glioblastoma cells, and/or HCT116 human colon tumor cells.
  • the L2G7 antibody when used as a single agent, will inhibit growth of various tumors by at least 25%, but possibly 40% or 50%, and as much as 75% or 90% or greater and may even cause tumor regression or disappearance.
  • Similar tumor inhibition experiments are performed with the anti-HGF antibody administered in combination one or more chemotherapeutic agents such as 5-FU (5-fluorouracil) or CPT-11 (Camptosar) to which the tumor type is expected to be responsive, as described by Ashkenize et al., J. Clin. Invest. 104:155, 1999.
  • the combination of the antibody and chemotherapeutic drug may produce a greater inhibition of ⁇ tumor growth than either agent alone.
  • the effect may be additive or synergistic, and strongly inhibit growth, e.g. by 80% or 90% or more, or even cause tumor regression or disappearance.
  • the anti-HGF antibody may also be administered in combination with an antibody against another growth or angiogenic factor, for example anti-VEGF, and additive or synergistic growth inhibition and/or tumor regression or disappearance is expected.

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US10/825,060 US20040208876A1 (en) 2003-04-18 2004-04-15 Monoclonal antibodies to hepatocyte growth factor
ZA200609407A ZA200609407B (en) 2004-04-15 2004-08-13 Monoclonal antibodies to hepatocyte growth factor
ES04781281T ES2346886T3 (es) 2004-04-15 2004-08-13 Anticuerpos monoclonales para el factor de crecimiento de hepatocitos.
PL04781281T PL1734995T3 (pl) 2004-04-15 2004-08-13 Przeciwciała monoklonalne wobec czynnika wzrostu hepatocytów
DE602004028168T DE602004028168D1 (de) 2004-04-15 2004-08-13 Monoklonale antikörper gegen den hepatozyten-wachstumsfaktor
NZ550324A NZ550324A (en) 2004-04-15 2004-08-13 Monoclonal antibodies to hepatocyte growth factor
MXPA06011822A MXPA06011822A (es) 2004-04-15 2004-08-13 Anticuerpos monoclonales al factor de crecimiento de hepatocito.
KR1020067023964A KR101072736B1 (ko) 2004-04-15 2004-08-13 간세포 성장 인자에 대한 단클론 항체
JP2007508323A JP4594381B2 (ja) 2004-04-15 2004-08-13 肝細胞増殖因子に対するモノクローナル抗体
US10/917,915 US7220410B2 (en) 2003-04-18 2004-08-13 Monoclonal antibodies to hepatocyte growth factor
DK04781281.3T DK1734995T3 (da) 2004-04-15 2004-08-13 Monoklonale antistoffer og hepatocyytvækstfaktor
EP10160203A EP2204191A1 (de) 2004-04-15 2004-08-13 Monoklonale Antikörper des Hepatocyten-Wachstumsfaktors
PCT/US2004/026565 WO2005107800A1 (en) 2004-04-15 2004-08-13 Monoclonal antibodies to hepatocyte growth factor
CNA200480042750XA CN1964738A (zh) 2004-04-15 2004-08-13 针对肝细胞生长因子的单克隆抗体
SI200431468T SI1734995T1 (sl) 2004-04-15 2004-08-13 Monoklonska protitelesa proti hepatocitnemu rastnemu faktorju
RU2006140257/13A RU2361879C2 (ru) 2004-04-15 2004-08-13 Моноклональные антитела к фактору роста гепатоцитов
CA2563080A CA2563080C (en) 2004-04-15 2004-08-13 Monoclonal antibodies to hepatocyte growth factor
BRPI0418745-8A BRPI0418745A (pt) 2004-04-15 2004-08-13 anticorpo linhagem de células, composição farmacêutica, e, método de tratamento de cáncer em um paciente
EP04781281A EP1734995B1 (de) 2004-04-15 2004-08-13 Monoklonale antikörper gegen den hepatozyten-wachstumsfaktor
AT04781281T ATE473760T1 (de) 2004-04-15 2004-08-13 Monoklonale antikörper gegen den hepatozyten- wachstumsfaktor
PT04781281T PT1734995E (pt) 2004-04-15 2004-08-13 Anticorpos monoclonais contra o factor de crescimento de hepatócitos
AU2004319276A AU2004319276C1 (en) 2004-04-15 2004-08-13 Monoclonal antibodies to hepatocyte growth factor
IL178474A IL178474A (en) 2004-04-15 2006-10-05 Monoclonal antibodies to hepatocyte growth factor and pharmaceutical compositions containing the same
CR8698A CR8698A (es) 2004-04-15 2006-10-19 Anticuerpos monoclonales al factor de crecimiento de hepatocito
NO20065227A NO20065227L (no) 2004-04-15 2006-11-14 Menoklonale antistoff mot hepatocytt vekstfaktor
HK07101333.7A HK1094167A1 (en) 2004-04-15 2007-02-05 Monoclonal antibodies to hepatocyte growth factor
US11/710,009 US7494650B2 (en) 2003-04-18 2007-02-23 Monoclonal antibodies to hepatocyte growth factor
US11/818,305 US7687063B2 (en) 2003-04-18 2007-06-13 Treating solid tumors with an antibody to hepatocyte growth factor
US12/342,059 US20090104192A1 (en) 2003-04-18 2008-12-22 Monoclonal Antibodies to Hepatocyte Growth Factor
JP2010174810A JP2011012067A (ja) 2004-04-15 2010-08-03 肝細胞増殖因子に対するモノクローナル抗体
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