DCision-making in tumors governs T cell anti-tumor immunity

被引:44
作者
Alfei, Francesca [1 ]
Ho, Ping-Chih [1 ,2 ]
Lo, Wan-Lin [3 ,4 ]
机构
[1] Univ Lausanne, Dept Oncol, Lausanne, Switzerland
[2] Univ Lausanne, Ludwig Inst Canc Res, Lausanne, Switzerland
[3] Univ Calif San Francisco, Dept Med, Div Rheumatol, Rosalind Russell & Ephraim P Engleman Arthrit Res, San Francisco, CA 94143 USA
[4] Univ Utah, Dept Pathol, Div Microbiol & Immunol, Salt Lake City, UT 84112 USA
基金
欧洲研究理事会;
关键词
PLASMACYTOID DENDRITIC CELLS; ENDOTHELIAL GROWTH-FACTOR; MELANOMA PROGRESSION; INHIBITORY RECEPTORS; DOWN-REGULATION; IFN-GAMMA; TGF-BETA; ANTIGEN; CANCER; CTLA-4;
D O I
10.1038/s41388-021-01946-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The exploitation of T cell-based immunotherapies and immune checkpoint blockade for cancer treatment has dramatically shifted oncological treatment paradigms and broadened the horizons of cancer immunology. Dendritic cells have emerged as the critical tailors of T cell immune responses, which initiate and coordinate anti-tumor immunity. Importantly, genetic alterations in cancer cells, cytokines and chemokines produced by cancer and stromal cells, and the process of tumor microenvironmental regulation can compromise dendritic cell-T cell cross-talk, thereby disrupting anti-tumor T cell responses. This review summarizes how T cell activation is controlled by dendritic cells and how the tumor microenvironment alters dendritic cell properties in the context of the anti-tumor immune cycle. Furthermore, we will highlight therapeutic options for tailoring dendritic cell-mediated decision-making in T cells for cancer treatment.
引用
收藏
页码:5253 / 5261
页数:9
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