| Literature DB >> 27163336 |
Albert T Gacerez1, Benjamine Arellano1, Charles L Sentman1.
Abstract
Chimeric antigen receptor (CAR) T cells have been developed to treat tumors and have shown great success against B cell malignancies. Exploiting modular designs and swappable domains, CARs can target an array of cell surface antigens and, upon receptor-ligand interactions, direct signaling cascades, thereby driving T cell effector functions. CARs have been designed using receptors, ligands, or scFv binding domains. Different regions of a CAR have each been found to play a role in determining the overall efficacy of CAR T cells. Therefore, this review provides an overview of CAR construction and common designs. Each CAR region is discussed in the context of its importance to a CAR's function. Additionally, the review explores how various engineering strategies have been applied to CAR T cells in order to regulate CAR T cell function and activity. J. Cell. Physiol. 231: 2590-2598, 2016.Entities:
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Year: 2016 PMID: 27163336 PMCID: PMC4993661 DOI: 10.1002/jcp.25419
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384