嵌合抗原受体
癌症研究
生物
免疫学
T细胞
免疫系统
作者
Huishan Li,Nicole M. L. Wong,Elliot P. Tague,John T. Ngo,Ahmad S. Khalil,Wilson Wong
出处
期刊:Cancer Cell
[Elsevier]
日期:2022-11-01
卷期号:40 (11): 1294-1305.e4
被引量:39
标识
DOI:10.1016/j.ccell.2022.08.008
摘要
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.
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