The cancer-immunity cycle: Indication, genotype, and immunotype

被引:404
作者
Mellman, Ira [1 ]
Chen, Daniel S. [2 ,3 ]
Powles, Thomas [4 ]
Turley, Shannon J. [1 ]
机构
[1] Genentech Inc, South San Francisco, CA 94080 USA
[2] Engenuity Life Sci, Burlingame, CA USA
[3] Synth Design Lab, Burlingame, CA USA
[4] Barts Canc Inst, London, England
关键词
T-CELL EXHAUSTION; DENDRITIC CELLS; TGF-BETA; PD-L1; BLOCKADE; TUMOR-CELLS; CD8+T CELLS; OPEN-LABEL; FIBROBLASTS; MACROPHAGES; THERAPY;
D O I
10.1016/j.immuni.2023.09.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The cancer-immunity cycle provides a framework to understand the series of events that generate anticancer immune responses. It emphasizes the iterative nature of the response where the killing of tumor cells by T cells initiates subsequent rounds of antigen presentation and T cell stimulation, maintaining active immunity and adapting it to tumor evolution. Any step of the cycle can become rate-limiting, rendering the immune system unable to control tumor growth. Here, we update the cancer-immunity cycle based on the remarkable progress of the past decade. Understanding the mechanism of checkpoint inhibition has evolved, as has our view of dendritic cells in sustaining anti-tumor immunity. We additionally account for the role of the tumor microenvironment in facilitating, not just suppressing, the anti-cancer response, and discuss the importance of considering a tumor's immunological phenotype, the "immunotype". While these new insights add some complexity to the cycle, they also provide new targets for research and therapeutic intervention.
引用
收藏
页码:2188 / 2205
页数:18
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