嵌合抗原受体
免疫疗法
淋巴因子激活杀伤细胞
免疫学
NK-92
白细胞介素15
免疫系统
自然杀伤细胞
Janus激酶3
白细胞介素12
白细胞介素21
生物
癌症研究
T细胞
细胞因子
白细胞介素
细胞毒性T细胞
体外
生物化学
作者
Minh Ma,Saiaditya Badeti,James K. Kim,Dongfang Liu
摘要
Chimeric antigen receptor (CAR)-modified immune cell therapy has become an emerging treatment for cancers and infectious diseases. NK-based immunotherapy, particularly CAR-NK cell, is one of the most promising 'off-the-shelf' development without severe life-threatening toxicity. However, the bottleneck for developing a successful CAR-NK therapy is achieving sufficient numbers of non-exhaustive, long-lived, 'off-the-shelf' CAR-NK cells from a third party. Here, we developed a new CAR-NK expansion method using an Epstein-Barr virus- (EBV) transformed B cell line expressing a genetically modified membrane form of interleukin-21 (IL-21). In this protocol, step-by-step procedures are provided to expand NK and CAR-NK cells from cord blood and peripheral blood, as well as solid organ tissues. This work will significantly enhance the clinical development of CAR-NK immunotherapy.
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