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CAR models: next-generation CAR modifications for enhanced T-cell function

期刊

MOLECULAR THERAPY-ONCOLYTICS
卷 3, 期 -, 页码 -

出版社

CELL PRESS
DOI: 10.1038/mto.2016.14

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资金

  1. H. Lee Moffitt Cancer Center and Research Institute
  2. American Society of Hematology
  3. Damon Runyon Cancer Research Foundation
  4. Moffitt's Lung Cancer Center of Excellence
  5. Career Enhancement Award from NIH SPORE [P50 CA168536]

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T cells genetically targeted with a chimeric antigen receptor (CAR) to B-cell malignancies have demonstrated tremendous clinical outcomes. With the proof in principle for CAR T cells as a therapy for B-cell malignancies being established, current and future research is being focused on adapting CAR technology to other cancers, as well as enhancing its efficacy and/or safety. The modular nature of the CAR, extracellular antigen-binding domain fused to a transmembrane domain and intracellular T-cell signaling domains, allows for optimization by replacement of the various components. These modifications are creating a whole new class of therapeutic CARs. In this review, we discuss the recent major advances in CAR design and how these modifications will impact its clinical application.

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