US2014234301A1PendingUtilityA1

Modulation of PILR to Treat Immune Disorders

Assignee: MERCK SHARP & DOHMEPriority: Dec 17, 2009Filed: Feb 14, 2014Published: Aug 21, 2014
Est. expiryDec 17, 2029(~3.4 yrs left)· nominal 20-yr term from priority
A61K 31/713C07K 2317/76C12N 2310/14C12N 2310/11C07K 2317/75C12N 15/1138C07K 2317/33C07K 16/2803C07K 2319/00C07K 2319/30C07K 16/28A61K 38/177
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Claims

Abstract

The present invention provides methods of using PILRα agonists, or PILRβ antagonists, to treat immune disorders, such as autoimmune and inflammatory disorders, including CNS, joint and gut inflammation.

Claims

exact text as granted — not AI-modified
1 . A method of treating an immune disorder comprising administering to a subject in need of such treatment an effective amount of an antagonist of PILRβ (SEQ ID NO: 4). 
     
     
         2 - 3 . (canceled) 
     
     
         4 . The method of  claim 1  wherein the antagonist of PILRβ comprises an antigen-binding domain from an antagonist antibody that specifically binds to PILRβ. 
     
     
         5 . The method of  claim 4  wherein the antagonist of PILRβ comprises an antibody. 
     
     
         6 . The method of  claim 4  wherein the antagonist of PILRβ comprises an antigen-binding domain from an antagonist antibody that specifically binds to PILRβ wherein the antagonist antibody is a chimeric, humanized, or fully human antibody. 
     
     
         7 . The method of claim  2  wherein the antagonist of PILRβ comprises a soluble polypeptide fragment of PILRβ (SEQ ID NO: 4). 
     
     
         8 - 13 . (canceled) 
     
     
         14 . The method of  claim 1  wherein the immune disorder is selected from the group consisting of:
 a) multiple sclerosis; 
 b) inflammatory bowel disease; 
 c) rheumatoid arthritis; 
 d) psoriasis; 
 e) insulin-dependent diabetes mellitus; 
 f) sarcoidosis; 
 g) systemic lupus erythematosus; 
 h) scleroderma; 
 i) allograft rejection; 
 j) autoimmune thyroid disease; 
 k) autoimmune uveitis; 
 l) scleritis; 
 m) autoimmune glomerulonephritis; 
 n) giant cell arteritis; and 
 o) airway hypersensitivity. 
 
     
     
         15 . The method of  claim 14 , wherein the immune disorder is selected from the group consisting of:
 a) multiple sclerosis;   b) inflammatory bowel disease; and   c) rheumatoid arthritis.   
     
     
         16 . The method of  claim 15 , wherein the immune disorder is multiple sclerosis. 
     
     
         17 . The method of  claim 15 , wherein the immune disorder is inflammatory bowel disease. 
     
     
         18 . The method of  claim 15 , wherein the immune disorder is rheumatoid arthritis. 
     
     
         19 - 21 . (canceled)

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