NK-92
细胞毒性T细胞
生物
MHC I级
免疫疗法
白细胞介素21
白细胞介素12
免疫学
癌症免疫疗法
主要组织相容性复合体
淋巴因子激活杀伤细胞
自然杀伤性T细胞
癌细胞
先天性淋巴细胞
Janus激酶3
先天免疫系统
免疫系统
癌症
T细胞
体外
生物化学
遗传学
作者
Natalie K. Wolf,Djem Kissiov,David H. Raulet
标识
DOI:10.1038/s41577-022-00732-1
摘要
Great strides have been made in recent years towards understanding the roles of natural killer (NK) cells in immunity to tumours and viruses. NK cells are cytotoxic innate lymphoid cells that produce inflammatory cytokines and chemokines. By lysing transformed or infected cells, they limit tumour growth and viral infections. Whereas T cells recognize peptides presented by MHC molecules, NK cells display receptors that recognize stress-induced autologous proteins on cancer cells. At the same time, their functional activity is inhibited by MHC molecules displayed on such cells. The enormous potential of NK cells for immunotherapy for cancer is illustrated by their broad recognition of stressed cells regardless of neoantigen presentation, and enhanced activity against tumours that have lost expression of MHC class I owing to acquired resistance mechanisms. As a result, many efforts are under way to mobilize endogenous NK cells with therapeutics, or to provide populations of ex vivo-expanded NK cells as a cellular therapy, in some cases by equipping the NK cells with chimeric antigen receptors. Here we consider the key features that underlie why NK cells are emerging as important new additions to the cancer therapeutic arsenal.
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