| Literature DB >> 22202074 |
Partow Kebriaei1, Susan S Kelly, Pallavi Manuri, Bipulendu Jena, Rineka Jackson, Elizabeth Shpall, Richard Champlin, Laurence J N Cooper.
Abstract
Adoptive transfer of antigen-specific T cells is a compelling tool to treat cancer. To overcome issues of immune tolerance which limits the endogenous adaptive immune response to tumor-associated antigens, robust systems for the genetic modification and characterization of T cells expressing chimeric antigen receptors (CARs) to redirect specificity have been produced. Refinements with regards to persistence and trafficking of the genetically modified T cells are underway to help improve the potency of genetically modified T cells. Clinical trials utilizing this technology demonstrate feasibility, and increasingly, antitumor activity, paving the way for multi-center trials to establish the efficacy of this novel T-cell therapy.Entities:
Mesh:
Substances:
Year: 2012 PMID: 22202074 PMCID: PMC3889487 DOI: 10.2741/282
Source DB: PubMed Journal: Front Biosci (Schol Ed) ISSN: 1945-0516