NZ764878B2 - Human monoclonal antibodies to ganglioside gd2 - Google Patents
Human monoclonal antibodies to ganglioside gd2Info
- Publication number
- NZ764878B2 NZ764878B2 NZ764878A NZ76487815A NZ764878B2 NZ 764878 B2 NZ764878 B2 NZ 764878B2 NZ 764878 A NZ764878 A NZ 764878A NZ 76487815 A NZ76487815 A NZ 76487815A NZ 764878 B2 NZ764878 B2 NZ 764878B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- antibody
- polypeptide
- conjugate
- exemplified
- domain
- Prior art date
Links
Classifications
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- 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
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- 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
- A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
- A61K39/39558—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against tumor tissues, cells, antigens
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/28—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/30—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
- C07K16/3076—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells against structure-related tumour-associated moieties
- C07K16/3084—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells against structure-related tumour-associated moieties against tumour-associated gangliosides
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
- C07K2317/21—Immunoglobulins specific features characterized by taxonomic origin from primates, e.g. man
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/33—Crossreactivity, e.g. for species or epitope, or lack of said crossreactivity
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
- C07K2317/565—Complementarity determining region [CDR]
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- 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
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- 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
- C07K2317/732—Antibody-dependent cellular cytotoxicity [ADCC]
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- 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
- C07K2317/734—Complement-dependent cytotoxicity [CDC]
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- 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
- C07K2317/77—Internalization into the cell
-
- 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
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2405/00—Assays, e.g. immunoassays or enzyme assays, involving lipids
- G01N2405/08—Sphingolipids
- G01N2405/10—Glycosphingolipids, e.g. cerebrosides, gangliosides
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- G01N33/57492—
Abstract
The present invention provides compositions for the production of an antibody or functional fragment thereof directed against disialoganglioside-GD2. The compositions of the invention include polynucleotides encoding a heavy chain and/or a light chain variable domain that binds to GD2. The invention also provides an isolated antibody or functional fragment thereof and methods of treating or preventing a disease, such as cancer or tumor formation, wherein the antibody or functional fragment includes a variable heavy chain domain and a variable light chain domain that has an amino acid sequence provided herein. The invention further provides a conjugate of an antibody or functional fragment thereof conjugated or recombinantly fused to a diagnostic agent, detectable agent or therapeutic agent, and methods of treating, preventing or diagnosing a disease in a subject in need thereof.
Claims (25)
1. An isolated antibody, or a polypeptide that binds to GD2 and comprises a onal fragment of the antibody, wherein said antibody or polypeptide comprises a combination of heavy chain variable domain (VH) and light chain variable domain (VL), the VH domain comprising VH CDR1, CDR2 and CDR3 according to residues 26-33, residues 51-58, and es 97-108 of SEQ ID NO: 30, and the VL domain sing VL CDR1, CDR2 and CDR3 according to residues 27-37, residues 55-57, and residues 94-102 of SEQ ID NO: 32.
2. The isolated antibody or polypeptide of claim 1, said antibody or polypeptide comprising the VH domain of SEQ ID NO: 30 and a VL domain of SEQ ID NO: 32.
3. The isolated antibody or polypeptide of claim 1 or 2, wherein said antibody is a human antibody.
4. The isolated antibody or polypeptide of claim 1 or 2, wherein said antibody functional fragment is selected from the group consisting of a Fab, a Fab', a 2, a scFV, a diabody, a triabody, and a minibody.
5. The isolated antibody or polypeptide of any one of claims 1-3, wherein said antibody is a onal dy.
6. The isolated antibody or polypeptide of any one of claims 1-3 or 5, wherein said antibody is an IgG or IgM isotope.
7. The isolated antibody or polypeptide of claim 6, wherein said IgG is an IgG 1subclass.
8. A conjugate comprising an isolated antibody or polypeptide of any one of claims 1-7 conjugated or recombinantly fused to a diagnostic agent, or detectable agent or therapeutic agent.
9. The conjugate of claim 8, wherein said antibody or polypeptide is conjugated or recombinantly fused to a detectable agent.
10. The use of a conjugate of claim 9, in the manufacture of a medicament for detecting a tumor in a subject in need thereof.
11. The ate of claim 8, wherein said antibody or polypeptide is conjugated or inantly fused to a therapeutic agent.
12. A pharmaceutical composition comprising the antibody or polypeptide of any one of claims 1-7, or the conjugate of claim 11, and a pharmaceutically acceptable carrier.
13. The use of an antibody or polypeptide according to any one of claims 1-7, the conjugate of claim 11 or the pharmaceutical ition of claim 12 in the cture of a medicament.
14. The use of an dy or polypeptide according to any one of claims 1-7, the conjugate of claim 11 or the pharmaceutical composition of claim 12, in the manufacture of a medicament for use in treating cancer, wherein the cells of said cancer express GD2.
15. The use of claim 14, n said cancer is selected from the group consisting of lastoma, osteosarcomas and other subsets of as, melanomas, gliomas, small cell lung cancer, breast cancer, medulloblastoma, and astrocytoma.
16. The use of claim 14 or 15, wherein said treatment comprises administering concurrently or successively a second therapeutic agent.
17. The use of claim 16, wherein said second therapeutic agent is a chemotherapeutic agent or an immunotherapeutic agent.
18. An isolated polynucleotide encoding the antibody or polypeptide of any one of claims 1-7.
19. An antibody or polypeptide according to claim 1, substantially as herein described or exemplified.
20. A conjugate according to claim 8, substantially as herein described or exemplified.
21. A use according to claim 10, substantially as herein described or exemplified.
22. A pharmaceutical composition according to claim 12, substantially as herein described or exemplified.
23. A use according to claim 13, substantially as herein described or exemplified.
24. A use ing to claim 14, substantially as herein described of exemplified.
25. An isolated polynucleotide according to claim 18, substantially as herein described or exemplified.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462007874P | 2014-06-04 | 2014-06-04 | |
| NZ726501A NZ726501B2 (en) | 2014-06-04 | 2015-06-03 | Human monoclonal antibodies to ganglioside gd2 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NZ764878A NZ764878A (en) | 2023-12-22 |
| NZ764878B2 true NZ764878B2 (en) | 2024-03-26 |
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