Targeting regulatory T cells in tumors

被引:183
作者
Liu, Chang [1 ]
Workman, Creg J. [1 ]
Vignali, Dario A. A. [1 ,2 ]
机构
[1] Univ Pittsburgh, Dept Immunol, Pittsburgh, PA USA
[2] Univ Pittsburgh, Inst Canc, Tumor Microenvironm Ctr, Pittsburgh, PA 15232 USA
基金
美国国家卫生研究院;
关键词
cancer immunotherapy; immune contexture; immunosuppression; regulatory T cells; tumor microenvironment; DENDRITIC CELLS; SUPPRESSOR-CELLS; PROGNOSTIC VALUE; CYCLOPHOSPHAMIDE TREATMENT; INFILTRATING LYMPHOCYTES; DENILEUKIN DIFTITOX; ANTITUMOR IMMUNITY; THYMIC DEVELOPMENT; IMPROVED SURVIVAL; PERIPHERAL-BLOOD;
D O I
10.1111/febs.13656
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
Regulatory T (T-reg) cells play a crucial role in maintaining peripheral tolerance and preventing autoimmunity. However, they also represent a major barrier to effective antitumor immunity and immunotherapy. Consequently, there has been considerable interest in developing approaches that can selectively or preferentially target Treg cells in tumors, while not impacting their capacity to maintain peripheral immune homeostasis. In this review, we describe our current understanding of the mechanisms underlying the recruitment, expansion, and suppressive activity of tumor-associated Treg cells, and discuss the approaches used and the challenges encountered in the immunotherapeutic targeting of Treg cells. In addition, we summarize the primary clinical targets and some emerging data on exciting new potential Treg cell-restricted targets. We propose that discovering and understanding mechanisms that are preferentially used by Treg cells within the tumor microenvironment will lead to strategies that selectively target Treg cell-mediated suppression of antitumor immunity while maintaining peripheral immune tolerance.
引用
收藏
页码:2731 / 2748
页数:18
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