US2004224009A1PendingUtilityA1

Devices comprising artificial antigen-presenting cellls

Priority: Oct 20, 1998Filed: Jul 7, 2003Published: Nov 11, 2004
Est. expiryOct 20, 2018(expired)· nominal 20-yr term from priority
G01N 33/56977A61K 47/6901Y10S424/812C12N 5/0006A61K 47/6911G01N 33/56972
49
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Claims

Abstract

The present invention is directed to artificial antigen presenting cells and methods of making artificial antigen presenting cells. Such artificial antigen presenting cells may be used in certain methods of isolating and expanding T cell populations as well as modulating T cell responses. Additionally, the present invention provides novel methods for the identification and isolation of antigen-specific T cells. The methods provide for the construction of liposomes containing MHC:peptide complexes, accessory molecules, co-stimulatory molecules, adhesion molecules, and other molecules irrelevant to T cell binding or modulation that are used in the binding of artificial antigen presenting cells to solid support systems that may be used in the retrieval and identification of antigen-specific T cells. Additionally, the present invention is directed to devices and methods for treating conditions which would benefit from modulation of T cell response, for example, autoimmune disorders, allergies, cancers, viral infections, and graft rejection.

Claims

exact text as granted — not AI-modified
1 - 11 . (Canceled)  
     
     
         12 . A device comprising: 
 a) a chamber that comprises a solid support; and    b) bound to the solid support, antigen presenting cells that comprise: 
 i. a liposome comprising a lipid bilayer comprised of neutral phospholipids and cholesterol;  
 ii. at least one GM-1 ganglioside molecule disposed in the lipid bilayer;  
 iii. a cholera toxin β subunit bound to a GM-1 ganglioside molecule;  
 iv. an MHC component loaded with an antigen of interest, wherein the antigen-loaded MHC component is bound to the cholera toxin β subunit;  
 V. an accessory molecule that can stabilize an interaction between a T cell receptor and the antigen-loaded MHC component; and  
 vi. an immunomodulatory molecule.

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