US2003077278A1PendingUtilityA1

Novel human beta2 integrin alpha subunit

Assignee: ICOS CORPPriority: Dec 23, 1993Filed: Jun 26, 2001Published: Apr 24, 2003
Est. expiryDec 23, 2013(expired)· nominal 20-yr term from priority
A61K 2039/505A01K 2217/05C07K 14/70553C07K 2319/00C07K 16/2845G01N 33/6893C12Q 1/6818G01N 2333/70553A61K 38/00
56
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Claims

Abstract

Methods to inhibit inflammation and macrophage infiltration following spinal cord injury are disclosed along with methods to modulate TNFα release from cells expressing α d are disclosed.

Claims

exact text as granted — not AI-modified
What is claimed is:  
     
         1 . A method for inhibiting macrophage infiltration at the site of a central nervous system injury comprising the step of administering to an individual an effective amount of an anti-α d  monoclonal antibody.  
     
     
         2 . The method according to claim I wherein the anti-α d  monoclonal antibody blocks binding between α d  and a binding partner.  
     
     
         3 . The method according to  claim 2  wherein the binding partner is VCAM-1.  
     
     
         4 . The method according to  claim 1  where the anti-α d  monoclonal antibody is selected from the group consisting of the monoclonal antibody secreted by hybridoma 226H and the monoclonal antibody secreted by hybridoma 236L.  
     
     
         5 . The method according to any one of claims  1  through  4  wherein the central nervous system injury is a spinal cord injury.  
     
     
         6 . A method for reducing inflammation at the site of a central nervous system injury comprising the step of administering to an individual an effective amount of an anti-α d  monoclonal antibody.  
     
     
         7 . The method according to  claim 6  wherein the anti-α d  monoclonal antibody blocks binding between α d  and a binding partner.  
     
     
         8 . The method according to  claim 7  wherein the binding partner is VCAM-1.  
     
     
         9 . The method according to  claim 6  where the anti-α d  monoclonal antibody is selected from the group consisting of the monoclonal antibody secreted by hybridoma 226H and the monoclonal antibody secreted by hybridoma 236L.  
     
     
         10 . The method according to any one of claims  6  through  9  wherein the central nervous system injury is a spinal cord injury.  
     
     
         11 . A method for modulating TNFα release from macrophages comprising the step of contacting said macrophages with an affective amount of an immunospecific ad monoclonal antibody.  
     
     
         12 . A method for modulating TNFα release from splenic phagocytes comprising the step of contacting said phagocytes with an affective amount of an immunospecific α d  monoclonal antibody.  
     
     
         13 . The method according to  claim 12  where in the anti-α d  monoclonal antibody inhibits TNFα release.  
     
     
         14 . The method according to  claim 13  wherein the immunospecific anti-α d  monoclonal antibody is selected from the group consisting of the monoclonal antibody secreted by hybridoma 205C and the monoclonal antibody secreted by hybridoma 205E.

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