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Chimeric Antigen Receptors: Driving Immunology Towards Synthetic Biology

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Publisher Elsevier
Date 2016 Jul 4
PMID 27372731
Citations 53
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Abstract

The advent of second generation chimeric antigen receptors and the CD19 paradigm have ushered a new therapeutic modality in oncology. In contrast to earlier forms of adoptive cell therapy, which were based on the isolation and expansion of naturally occurring T cells, CAR therapy is based on the design and manufacture of engineered T cells with optimized properties. A new armamentarium, comprising not only CARs but also chimeric costimulatory receptors, chimeric cytokine receptors, inhibitory receptors and synthetic Notch receptors, expressed in naïve, central memory or stem cell-like memory T cells, is being developed for clinical use in a wide range of cancers. Immunological principles are thus finding a new purpose thanks to advances in genetic engineering, synthetic biology and cell manufacturing sciences.

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References
1.
Sadelain M . CAR therapy: the CD19 paradigm. J Clin Invest. 2015; 125(9):3392-400. PMC: 4588281. DOI: 10.1172/JCI80010. View

2.
Brocker T . Chimeric Fv-zeta or Fv-epsilon receptors are not sufficient to induce activation or cytokine production in peripheral T cells. Blood. 2000; 96(5):1999-2001. View

3.
Morsut L, Roybal K, Xiong X, Gordley R, Coyle S, Thomson M . Engineering Customized Cell Sensing and Response Behaviors Using Synthetic Notch Receptors. Cell. 2016; 164(4):780-91. PMC: 4752866. DOI: 10.1016/j.cell.2016.01.012. View

4.
Ramos C, Savoldo B, Dotti G . CD19-CAR trials. Cancer J. 2014; 20(2):112-8. PMC: 3979594. DOI: 10.1097/PPO.0000000000000031. View

5.
Miller J, Sadelain M . The journey from discoveries in fundamental immunology to cancer immunotherapy. Cancer Cell. 2015; 27(4):439-49. DOI: 10.1016/j.ccell.2015.03.007. View