Qian Liling, Chen Jiangqing, Wu Xiaoyan, Jing Ruirui, Sun Jie
Bone Marrow Transplantation Center of the First Affiliated Hospital, and Department of Cell Biology, Zhejiang University School of Medicine, Hangzhou 310058, Zhejiang, China.
Institute of Hematology, Zhejiang University & Laboratory of Stem Cell and Immunotherapy Engineering, Hangzhou 310058, Zhejiang, China.
Sheng Wu Gong Cheng Xue Bao. 2019 Dec 25;35(12):2339-2349. doi: 10.13345/j.cjb.190291.
Chimeric antigen receptor T (CAR-T) cell therapy, which adoptively transfers engineered T cells expressing synthetic receptors to target specific antigens, has achieved great clinical success in treating hematological malignancies. Though FDA has approved two CAR-T products, CAR-T therapy can cause some side effects, such as cytokine release syndrome (CRS), neurotoxicity and B cell aplasia. Meanwhile, lacking tumor specific antigen and the suppressive tumor environment limit the efficacy of CAR-T therapy in solid tumor. This review focuses on the structural components, clinical applications and synthetic biology approaches on CAR-T cell design, and summarizes the challenges and perspectives of CAR-T therapy as a revolutionary cancer immunotherapy.
嵌合抗原受体T(CAR-T)细胞疗法是将表达合成受体的工程化T细胞过继性转移以靶向特定抗原,在治疗血液系统恶性肿瘤方面取得了巨大的临床成功。尽管美国食品药品监督管理局(FDA)已批准了两种CAR-T产品,但CAR-T疗法会引发一些副作用,如细胞因子释放综合征(CRS)、神经毒性和B细胞发育不全。同时,缺乏肿瘤特异性抗原以及肿瘤抑制环境限制了CAR-T疗法在实体瘤中的疗效。本文综述聚焦于CAR-T细胞设计的结构组成、临床应用和合成生物学方法,并总结了CAR-T疗法作为一种革命性癌症免疫疗法所面临的挑战和前景。