T-cell exhaustion in the tumor microenvironment

被引:864
作者
Jiang, Y. [1 ]
Li, Y. [1 ,2 ,3 ]
Zhu, B. [1 ]
机构
[1] Third Mil Med Univ, Inst Canc, Xinqiao Hosp, Chongqing, Peoples R China
[2] Brigham & Womens Hosp, Harvard Inst Med, Ctr Expt Therapeut & Reperfus Injury Perioperat &, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
基金
中国国家自然科学基金;
关键词
TGF-BETA; IMMUNE SUPPRESSION; UP-REGULATION; LIGAND; POSTOPERATIVE RECURRENCE; CLINICAL-SIGNIFICANCE; INHIBITORY RECEPTORS; PD-1; EXPRESSION; POOR-PROGNOSIS; DEATH;
D O I
10.1038/cddis.2015.162
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
T-cell exhaustion was originally identified during chronic infection in mice, and was subsequently observed in humans with cancer. The exhausted T cells in the tumor microenvironment show overexpressed inhibitory receptors, decreased effector cytokine production and cytolytic activity, leading to the failure of cancer elimination. Restoring exhausted T cells represents an inspiring strategy for cancer treatment, which has yielded promising results and become a significant breakthrough in the cancer immunotherapy. In this review, we overview the updated understanding on the exhausted T cells in cancer and their potential regulatory mechanisms and discuss current therapeutic interventions targeting exhausted T cells in clinical trials.
引用
收藏
页码:e1792 / e1792
页数:9
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