The ability to control T cells engineered to permanently express chimeric antigen receptors (CARs) is a key feature to improve safety. Here, we describe the development of a new CAR architecture with an integrated switch-on system that permits to control the CAR T-cell function. This system offers the advantage of a transient CAR T-cell for safety while letting open the possibility of multiple cytotoxicity cycles using a small molecule drug.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707440PMC
http://dx.doi.org/10.1038/srep18950DOI Listing

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