US2016185846A1PendingUtilityA1

Antibodies against monocyte chemotactic proteins

Assignee: BIOGEN MA INCPriority: Nov 30, 2001Filed: Jun 22, 2015Published: Jun 30, 2016
Est. expiryNov 30, 2021(expired)· nominal 20-yr term from priority
A61P 9/10A61P 37/00A61P 37/06A61P 35/00A61P 25/00A61P 29/00A61P 1/16C07K 2317/55A61K 2039/505C07K 2317/76C07K 2317/31C07K 2317/24C07K 2317/565C07K 16/24A61P 19/02A61P 21/00C07K 2317/56A61P 1/00A61P 17/00C07K 2317/92A61P 19/04
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Claims

Abstract

The invention provides antibodies that bind to a plurality of β-chemokines, particularly monocyte chemotactic proteins MCP-1, MCP-2 and MCP-3. The invention also provides cells producing the antibodies, and methods of making and using the same.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A monoclonal antibody or antigen-binding fragment thereof comprising a heavy chain variable region having a CDR1 domain comprising the sequence set forth in SEQ ID NO:13, a CDR2 domain comprising the sequence set forth in SEQ ID NO:14, and a CDR3 domain comprising the sequence set forth in SEQ ID NO:15. 
     
     
         2 . The antibody or antigen binding fragment of  claim 1 , wherein the heavy chain variable region comprises the sequence set forth in SEQ ID NO:11. 
     
     
         3 . A monoclonal antibody or antigen-binding fragment thereof comprising a light chain variable region having a CDR1 domain comprising the sequence set forth in SEQ ID NO:16, a CDR2 domain comprising the sequence set forth in SEQ ID NO:17, and a CDR3 domain comprising the sequence set forth in SEQ ID NO:18. 
     
     
         4 . The antibody or antigen binding fragment of  claim 3 , wherein the light chain variable region comprises the sequence set forth in SEQ ID NO:12. 
     
     
         5 . The antibody or antigen binding fragment of  claim 1 , further comprising a light chain variable region having a CDR1 domain comprising the sequence set forth in SEQ ID NO:16, a CDR2 domain comprising the sequence set forth in SEQ ID NO:17, and a CDR3 domain comprising the sequence set forth in SEQ ID NO:18. 
     
     
         6 . The antibody or antigen binding fragment of  claim 2 , further comprising a light chain variable region comprising the sequence set forth in SEQ ID NO:12 
     
     
         7 . The antibody or antigen binding fragment of  claim 5 , wherein the antibody binds to MCP-1 and at least one other β-chemokine. 
     
     
         8 . The antibody or antigen binding fragment of  claim 7 , wherein the at least one other β-chemokine includes MCP-2. 
     
     
         9 . The antibody or antigen binding fragment of  claim 5 , wherein the antibody binds to MCP-1, MCP-2, and MCP-3. 
     
     
         10 . The antibody or antigen binding fragment of  claim 5 , wherein the antibody is a chimeric antibody. 
     
     
         11 . The antibody or antigen binding fragment of  claim 5 , wherein the antibody is a humanized antibody. 
     
     
         12 . The antigen binding fragment of  claim 5 , wherein the fragment is selected from a Fab fragment, a Fab′ fragment, a F(ab) 2  fragment, and a F v  fragment. 
     
     
         13 . A method of reducing chemotaxis in a subject suffering from a disorder selected from glomerulonephritis, scleroderma, cirrhosis, multiple sclerosis, lupus nephritis, atherosclerosis, inflammatory bowel disease or rheumatoid arthritis, comprising administering to the subject the antibody or antigen binding fragment thereof according to any one of  claims 1 - 12 . 
     
     
         14 . A method of reducing chemotaxis in a subject suffering from a disorder selected from glomerulonephritis, scleroderma, cirrhosis, multiple sclerosis, lupus nephritis, atherosclerosis, inflammatory bowel disease or rheumatoid arthritis, comprising administering to the subject the antibody or antigen binding fragment thereof comprising
 a) a heavy chain variable region having a CDR1 domain comprising the sequence set forth in SEQ ID NO:13, a CDR2 domain comprising the sequence set forth in SEQ ID NO:14, and a CDR3 domain comprising the sequence set forth in SEQ ID NO:15; and   b) a light chain variable region having a CDR1 domain comprising the sequence set forth in SEQ ID NO:16, a CDR2 domain comprising the sequence set forth in SEQ ID NO:17, and a CDR3 domain comprising the sequence set forth in SEQ ID NO:18.   
     
     
         15 . The method of  claim 14 , wherein the heavy variable region comprises the sequence set forth in SEQ ID NO:11, and the light chain variable region comprises the sequence set forth in SEQ ID NO:12.

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