US2017027988A1PendingUtilityA1

Immunotherapy of cancer using genetically engineered gd2-specific t cells

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Assignee: BAYLOR COLLEGE MEDICINEPriority: Sep 8, 2010Filed: Oct 13, 2016Published: Feb 2, 2017
Est. expirySep 8, 2030(~4.1 yrs left)· nominal 20-yr term from priority
C07K 16/18C07K 2317/622C07K 16/3084A61K 39/0011A61K 2039/5156C12N 5/0638A61K 35/17A61K 40/4273A61K 40/4272A61K 40/4268A61K 40/4258A61K 40/31A61K 40/11A61K 2239/55A61K 2239/57
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Claims

Abstract

The present invention concerns immunotherapy for cancers having cells that comprise the ganglioside GD2 antigen. In specific embodiment, T cells having a chimeric receptor that targets GD2 is employed. In particular cases, the chimeric receptor comprises antibody, cytoplasmic signaling domain from the T cell receptor, and/or costimulatory molecule(s).

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of targeting a cancer cell having a GD2 antigen, comprising the steps of providing to the cell a cytotoxic T lymphocyte with a chimeric receptor that recognizes the GD2 antigen. 
     
     
         2 . The method of  claim 1 , wherein the cancer cell is in vitro or in vivo. 
     
     
         3 . The method of  claim 1 , wherein the chimeric receptor comprises antibody that binds GD2 
     
     
         4 . The method of  claim 2 , wherein the antibody is a scFv antibody. 
     
     
         5 . The method of  claim 2 , wherein the antibody is the 14g2a scFv antibody. 
     
     
         6 . The method of  claim 1 , wherein the chimeric receptor comprises the effector domain of the T-cell receptor zeta chain or related signal transduction endodomains derived from the T cell receptor. 
     
     
         7 . The method of  claim 1 , wherein the chimeric receptor comprises one or more costimulatory molecules. 
     
     
         8 . The method of  claim 6 , wherein the costimulatory molecules comprise CD28, OX40, 4-1BB, or a combination thereof.

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