1. Academic Validation
  2. High-performance multiplex drug-gated CAR circuits

High-performance multiplex drug-gated CAR circuits

  • Cancer Cell. 2022 Aug 26;S1535-6108(22)00372-5. doi: 10.1016/j.ccell.2022.08.008.
Hui-Shan Li 1 Nicole M Wong 1 Elliot Tague 1 John T Ngo 1 Ahmad S Khalil 2 Wilson W Wong 3
Affiliations

Affiliations

  • 1 Department of Biomedical Engineering and Biological Design Center, Boston University, Boston, MA, USA.
  • 2 Department of Biomedical Engineering and Biological Design Center, Boston University, Boston, MA, USA; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
  • 3 Department of Biomedical Engineering and Biological Design Center, Boston University, Boston, MA, USA. Electronic address: wilwong@bu.edu.
Abstract

Chimeric antigen receptor (CAR) T cells can revolutionize Cancer medicine. However, overactivation, lack of tumor-specific surface markers, and antigen escape have hampered CAR T cell development. A multi-antigen targeting CAR system regulated by clinically approved pharmaceutical agents is needed. Here, we present VIPER CARs (versatile Protease regulatable CARs), a collection of inducible ON and OFF switch CAR circuits engineered with a viral Protease domain. We established their controllability using FDA-approved antiviral Protease Inhibitors in a xenograft tumor and a cytokine release syndrome mouse model. Furthermore, we benchmarked VIPER CARs against other drug-gated systems and demonstrated best-in-class performance. We showed their orthogonality in vivo using the ON VIPER CAR and OFF lenalidomide-CAR systems. Finally, we engineered several VIPER CAR circuits by combining various CAR technologies. Our multiplexed, drug-gated CAR circuits represent the next progression in CAR design capable of advanced logic and regulation for enhancing the safety of CAR T cell therapy.

Keywords

CAR; gene circuits; immunotherapy; synthetic biology.

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