Regulatory T Cells and Cancer: A Two-Sided Story

被引:37
|
作者
Wang, Kepeng [1 ]
Vella, Anthony T. [1 ]
机构
[1] Univ Connecticut, Sch Med, Dept Immunol, Ctr Hlth, 263 Farmington Ave, Farmington, CT 06030 USA
关键词
Cancer immunotherapy; cytokines; inflammation; regulatory T cells; NF-KAPPA-B; GROWTH-FACTOR-BETA; TGF-BETA; COLON-CANCER; COLORECTAL-CANCER; MOLECULAR-MECHANISMS; CYTOKINE PRODUCTION; ULCERATIVE-COLITIS; INTERFERON-GAMMA; SIGNAL-TRANSDUCTION;
D O I
10.1080/08820139.2016.1197242
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T cells (Tregs) play pivotal roles in limiting the duration and magnitude of immune response against infectious agents and self-antigens. This is accomplished through contact-dependent and -independent mechanisms that involve crosstalk between Treg cells and other immune and tissue-specific cell types. The same machinery is employed by Tregs to regulate immune responses to cancer, limiting both pro-tumor inflammation and anti-tumor immunity. Factors produced by Treg cells also act directly on transformed epithelial cells and exert opposing effects during different stages of cancer development. Therefore, the immune regulatory cell population serves as a double-edged sword for the development, progression, and treatment of cancers. In this review, we summarize current knowledge on the roles of Treg lymphocytes during cancer development, as well as the underlying cellular and molecular mechanism.
引用
收藏
页码:797 / 812
页数:16
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