US2013195895A1PendingUtilityA1

Methods of modulating immune responses by modulating tim-1, tim-2 and tim-4 function

Assignee: BRIGHAM & WOMENS HOSPITALPriority: Mar 12, 2004Filed: Jan 25, 2013Published: Aug 1, 2013
Est. expiryMar 12, 2024(expired)· nominal 20-yr term from priority
A61P 31/14A61P 7/00A61P 37/06A61P 35/00A61P 37/00A61P 31/20A61P 5/14A61P 7/06A61P 31/16A61P 37/02A61P 35/02A61P 9/10A61P 7/04A61P 3/10A61P 37/08A61P 27/16A61P 29/00A61P 25/00A61P 27/02G01N 2500/02A61P 11/06A61P 17/06C12N 2310/14A61P 1/16C07K 16/2875G01N 33/6863A61P 11/02A61P 13/12A61K 38/00A61K 39/3955A61P 19/02C07K 14/70503C07K 2319/00A61P 1/04G01N 2800/24A61P 15/00G01N 33/6845A61P 17/04A61P 17/00A61K 38/177A61K 39/39541A61K 2039/505G01N 33/6812G01N 33/6872C07K 16/2803A61P 1/00G01N 33/5768A61K 48/00A61P 21/04
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Claims

Abstract

The invention relates to methods of modulating immune responses in a subject such as by administering to the subject agents which modulate tim-1, tim-2 or tim-4 activity, or which modulate the physical interaction between tim-1 and tim-4 or between tim-2 and a tim-2 ligand. Immune responses include, but are not limited to, autoimmune disorders, transplantation tolerance, and Th1 and Th2-mediated responses and disorders. The invention also relates to novel assays for identifying agents which modulate the physical interaction between tim-1 and tim-4. In addition, the invention relates to novel soluble tim-4 polypeptides and to nucleic acids which encode them.

Claims

exact text as granted — not AI-modified
1 . A method of increasing immune tolerance in a subject in need thereof, the method comprising administering to such subject a therapeutically effective amount of a polypeptide agent that inhibits the activity or expression of tim-4, whereby immune tolerance in said subject is increased. 
     
     
         2 . The method of  claim 1 , wherein said subject suffers from an autoimmune disease, and wherein said increase in immune tolerance treats said autoimmune disease. 
     
     
         3 . The method of  claim 1 , wherein said subject is a transplant recipient, and whereby said increase in immune tolerance increases transplant tolerance. 
     
     
         4 . The method of  claim 1 , wherein said polypeptide agent comprises an antibody or antigen-binding fragment thereof that specifically binds to tim-4. 
     
     
         5 . The method of  claim 1 , wherein the polypeptide agent reduces binding of tim-4 to tim-1. 
     
     
         6 . The method of  claim 1 , wherein said polypeptide agent comprises a soluble tim-1 molecule. 
     
     
         7 . The method of  claim 6 , wherein the soluble tim-1 polypeptide comprises (i) amino acids 21-126 of SEQ ID NO: 1 or (ii) amino acids 21-129 of SEQ ID NO: 2. 
     
     
         8 . The method of  claim 1 , wherein the polypeptide agent further comprises (a) human serum albumin; or (b) an Fc domain of an immunoglobulin. 
     
     
         9 . The method of  claim 2 , wherein said autoimmune disease is selected from the group consisting of type-I diabetes, multiple sclerosis, systemic lupus erythematosus, rheumatoid arthritis, and Crohn's disease. 
     
     
         10 . A method of increasing immune tolerance in a subject in need thereof, the method comprising administering to such subject a therapeutically effective amount of a polypeptide agent that inhibits the activity or expression of tim-1, whereby immune tolerance in said subject is increased. 
     
     
         11 . The method of  claim 10 , wherein said subject suffers from an autoimmune disease, and wherein said increase in immune tolerance treats said autoimmune disease. 
     
     
         12 . The method of  claim 10 , wherein said subject is a transplant recipient, and whereby said increase in immune tolerance increases transplant tolerance. 
     
     
         13 . The method of  claim 10 , wherein said polypeptide agent comprises an antibody or antigen-binding fragment thereof that specifically binds to and blocks the activity of tim-1. 
     
     
         14 . The method of  claim 10 , wherein the polypeptide agent reduces binding of tim-1 to tim-4. 
     
     
         15 . The method of  claim 10 , wherein said polypeptide agent comprises a soluble tim-1 molecule. 
     
     
         16 . The method of  claim 15 , wherein the soluble tim-1 polypeptide comprises (i) amino acids 21-126 of SEQ ID NO: 1 or (ii) amino acids 21-129 of SEQ ID NO: 2. 
     
     
         17 . The method of  claim 10 , wherein the polypeptide agent further comprises (a) human serum albumin; or (b) an Fc domain of an immunoglobulin. 
     
     
         18 . The method of  claim 11 , wherein said autoimmune disease is selected from the group consisting of type-I diabetes, multiple sclerosis, systemic lupus erythematosus, rheumatoid arthritis, and Crohn's disease. 
     
     
         19 . A method of decreasing, inhibiting, suppressing, ameliorating, or delaying a Th1-mediated immune response in a subject in need thereof, comprising administering to a subject in need thereof a therapeutically effective amount of a tim-1 or tim-4 antagonist that binds tim-1 or tim-4 in an amount sufficient to decrease, inhibit, suppress, ameliorate, or delay a Th1-mediated response in the subject by reducing the expression or activity of tim-1 or tim-4. 
     
     
         20 . The method of  claim 19 , wherein the tim-1 or tim-4 antagonist is selected from the group consisting of an antibody or antigen-binding fragment thereof that binds the tim-1 or tim-4 extracellular domain, and a soluble tim-1 polypeptide.

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