嵌合抗原受体
癌症研究
细胞因子释放综合征
细胞因子
体内
化学
细胞生物学
免疫疗法
免疫系统
医学
免疫学
生物
生物技术
作者
Xinyue Wang,Fanyan Meng,Xiang Li,Luxin Xue,Anni Chen,Yuling Qiu,Zhifan Zhang,Lin Li,Fengcen Liu,Yishan Li,Zhichen Sun,Yanhong Chu,Ruihan Xu,Lixia Yu,Jie Shao,Manman Tian,Xiaoping Qian,Qin Liu,Baorui Liu,Rutian Li
标识
DOI:10.1002/advs.202205044
摘要
Chimeric antigen receptor (CAR)-T cell therapy is a transformative treatment against advanced malignancies. Unfortunately, once administrated in vivo, CAR-T cells become out of artificial control, and fierce response to CAR-T therapy may cause severe adverse events, represented by cytokine-release syndrome and on-target/off-tumor effects. Here, a nanomodified switch strategy is developed, leading to sustained and precise "on-tumor only" activation of CAR-T cells. Here, original gelatinase-responsive nanoparticles (NPs) are used to selectively deliver the heterodimerizing switch, which is the key component of switchable CAR with separated activation modules. The "NanoSwitch" is tumor-specific, thus inactivated switchable CAR-T cells do little harm to normal cells, even if the normal cells express the target of CAR-T. Owing to the sustained-release effect of NPs, the CAR-T cells are activated smoothly, avoiding sudden release of cytokine. These data introduce NanoSwitch as a universal and applicable solution to safety problems of CAR-T therapy regardless of the target.
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