NKG2D公司
提吉特
生物
细胞毒性T细胞
白细胞介素21
NK-92
免疫学
CD8型
白细胞介素12
癌症免疫疗法
免疫疗法
免疫系统
淋巴因子激活杀伤细胞
自然杀伤性T细胞
癌症研究
抗原提呈细胞
T细胞
细胞生物学
体外
生物化学
作者
Oleksandr Kyrysyuk,Kai W. Wucherpfennig
出处
期刊:Annual Review of Immunology
[Annual Reviews]
日期:2023-04-26
卷期号:41 (1): 17-38
被引量:36
标识
DOI:10.1146/annurev-immunol-101921-044122
摘要
T cells and natural killer (NK) cells have complementary roles in tumor immunity, and dual T cell and NK cell attack thus offers opportunities to deepen the impact of immunotherapy. Recent work has also shown that NK cells play an important role in recruiting dendritic cells to tumors and thus enhance induction of CD8 T cell responses, while IL-2 secreted by T cells activates NK cells. Targeting of immune evasion mechanisms from the activating NKG2D receptor and its MICA and MICB ligands on tumor cells offers opportunities for therapeutic intervention. Interestingly, T cells and NK cells share several important inhibitory and activating receptors that can be targeted to enhance T cell– and NK cell–mediated immunity. These inhibitory receptor-ligand systems include CD161-CLEC2D, TIGIT-CD155, and NKG2A/CD94-HLA-E. We also discuss emerging therapeutic strategies based on inhibitory and activating cytokines that profoundly impact the function of both lymphocyte populations within tumors.
科研通智能强力驱动
Strongly Powered by AbleSci AI