IP Library Granted Patent US 7,482,434
Granted Patent B2
US 7,482,434 · App. 11/641,128 · Granted Jan 27, 2009

Antibodies directed to monocyte chemo-attractant protein-1 (MCP-1) and uses thereof

Assignee: AstraZeneca AB
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Quick Facts
Patent No.
US 7,482,434
App. No.
11/641,128
Granted
Jan 27, 2009
Kind
B2
Abstract

Embodiments of the invention described herein relate to antibodies directed to the antigen monocyte chemo-attractant protein-1 (MCP-1) and uses of such antibodies. In particular, in accordance with some embodiments, there are provided fully human monoclonal antibodies directed to the antigen MCP-1. Nucelotide sequences encoding, and amino acid sequences comprising, heavy and light chain immunoglobulin molecules, particularly sequences corresponding to contiguous heavy and light chain sequences spanning the framework regions and/or complementarity determining regions (CDRs), specifically from FR1 through FR4 or CDR1 through CDR3, are provided. Hybridomas or other cell lines expressing such immunoglobulin molecules and monoclonal antibodies are also provided.

Claims (33)

1. An isolated human monoclonal antibody that binds to MCP-1 and comprises a heavy chain polypeptide having the sequence of SEQ ID NO: 38.

2. The antibody of claim 1 , further comprising a light chain polypeptide having the sequence of SEQ ID NO: 40.

3. An isolated antibody immobilized on an insoluble matrix, wherein the antibody is the antibody of claim 2 .

4. A method for assaying the level of monocyte chemo-attractant protein-1 (MCP-1) in a patient sample, comprising:

contacting the anti-MCP-1 antibody of claim 2 with the patient sample, and

detecting the level of MCP-1 in the patient sample.

5. A method according to claim 4 wherein the patient sample is blood.

6. A composition, comprising the antibody of claim 2 , and a pharmaceutically acceptable carrier.

7. A method of treating a neoplastic disease, comprising:

selecting an animal in need of treatment for a neoplastic disease; and

administering to said animal a therapeutically effective dose of the fully human monoclonal antibody of claim 1 .

8. The method of claim 7 , wherein said neoplastic disease is selected from the group consisting of: breast cancer, ovarian cancer, bladder cancer, lung cancer, glioblastoma, stomach cancer, endometrial cancer, kidney cancer, colon cancer, pancreatic cancer, and prostate cancer.

9. A method of treating inflammatory conditions, comprising:

selecting an animal in need of treatment for an inflammatory condition; and

administering to said animal a therapeutically effective dose of the fully human monoclonal antibody of claim 1 .

10. The method of claim 9 , wherein said inflammatory condition is selected from the group consisting of: rheumatoid arthritis, glomerulonephritis, atherosclerosis, psoriasis, restenosis, autoimmune disease, and multiple sclerosis.

11. An isolated human monoclonal antibody that cross-competes for binding to MCP-1, wherein said antibody comprises a heavy chain polypeptide having the sequence of SEQ ID NO.: 38.

12. The antibody of claim 11 , wherein said antibody further comprises a light chain polypeptide having the sequence of SEQ ID NO.: 40.

13. A method of manufacturing the antibody of claim 1 , comprising:

immunizing a mammal with a synthetic peptide of MCP-1;

recovering lymphatic cell that expresses the antibody of claim 1 from the immunized mammal; and

fusing the lymphatic cell with a myeloid-type cell to prepare a hybridoma cell that produces the antibody of claim 1 .

14. The antibody of claim 1 , wherein said antibody is conjugated to a therapeutic agent.

15. The antibody of claim 14 , wherein said therapeutic agent is a toxin.

16. The antibody of claim 15 , wherein said toxin is an immunotoxin.

17. The antibody of claim 14 , wherein said therapeutic agent is a chemotherapeutic agent.

18. The antibody of claim 17 , wherein said chemotherapeutic agent is selected from the group consisting of taxol, doxorubicin, cis-platinum, and 5-fluorouracil.

19. The antibody of claim 14 , wherein said therapeutic agent is a radioisotope.

20. The antibody of claim 19 , wherein said radioisotope is selected from the group consisting of 3H, 14C, 15N, 35S, 90Y, 99Tc, 111In, 125In, and 131I.

21. An isolated human monoclonal antigen binding fragment that binds to MCP-1 and comprises a heavy chain polypeptide having the sequence of SEQ ID NO: 38.

22. The antigen binding fragment of claim 21 , further comprising a light chain polypeptide having the sequence of SEQ ID NO: 40.

23. The antigen binding fragment of claim 21 , wherein said binding fragment is selected from the group consisting of Fab, Fab′, F(ab′)2, and Fv.

24. The antigen binding fragment of claim 23 , wherein said fragment is conjugated to a therapeutic agent.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 10, 2011
From: ASTRAZENECA AB
To: MEDIMMUNE LIMITED
Reel/Frame 025788/0700 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 9, 2007
From: AMGEN FREMONT INC.
To: ASTRAZENECA AB
Reel/Frame 019269/0091 →
MERGER Recorded Mar 15, 2007
From: ABGENIX, INC.
To: AMGEN FREMONT INC.
Reel/Frame 019027/0528 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 14, 2007
From: GUDAS, JEAN M.; HAAK-FRENDSCHO, MARY; FOORD, ORIT; LIANG, MEINA L.; AHLUWALIA, KIRAN; BHAKTA, SUNIL
To: ABGENIX, INC.
Reel/Frame 019014/0439 →
Continuity (3)
Division 1064427700 · Aug 19, 2003
Provisional Application 6040480200 · Aug 19, 2002
Related Publication 20070128112A1 · Jun 7, 2007