嵌合抗原受体
诱导多能干细胞
免疫疗法
癌症免疫疗法
过继性细胞移植
免疫系统
细胞疗法
免疫学
癌症研究
生物
医学
T细胞
干细胞
胚胎干细胞
细胞生物学
基因
生物化学
作者
Xiaotong Lin,Yao Sun,Xin Dong,Z. Liu,Ryohichi Sugimura,Guozhu Xie
标识
DOI:10.1016/j.biopha.2023.115123
摘要
Adoptive cell therapies (ACT) based on chimeric antigen receptor (CAR)-modified immune cells have made great progress with six CAR-T cell products approved by the U.S. FDA for hematological malignancies. Compared with CAR-T cells, CAR-NK cells have attracted increasing attention owing to their multiple killing mechanisms, higher safety profile, and broad sources. Induced pluripotent stem cell (iPSC)-derived NK (iPSC-NK) cells possess a mature phenotype and potent cytolytic activity, and can provide a homogeneous population of CAR-NK cells that can be expanded to clinical scale. Thus, iPSC-derived CAR-NK (CAR-iNK) cells could be used as a standardized and "off-the-shelf" product for cancer immunotherapy. In this review, we summarize the current status of the manufacturing techniques, genetic modification strategies, preclinical and clinical evidence of CAR-iNK cells, and discuss the challenges and future prospects of CAR-iNK cell therapy as a novel cellular immunotherapy in cancer.
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