共 50 条
The cancer-immunity cycle: Indication, genotype, and immunotype
被引:260
|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
来源:
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
相关论文