Wang Kepeng, Vella Anthony T
a Department of Immunology , School of Medicine, University of Connecticut Health Center , Farmington , CT , USA.
Immunol Invest. 2016 Nov;45(8):797-812. doi: 10.1080/08820139.2016.1197242. Epub 2016 Sep 7.
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.
调节性T细胞(Tregs)在限制针对感染因子和自身抗原的免疫反应的持续时间和强度方面发挥着关键作用。这是通过依赖接触和不依赖接触的机制来实现的,这些机制涉及调节性T细胞与其他免疫和组织特异性细胞类型之间的相互作用。调节性T细胞利用相同的机制来调节对癌症的免疫反应,限制促肿瘤炎症和抗肿瘤免疫。调节性T细胞产生的因子也直接作用于转化的上皮细胞,并在癌症发展的不同阶段发挥相反的作用。因此,免疫调节细胞群体在癌症的发生、发展和治疗中是一把双刃剑。在这篇综述中,我们总结了关于调节性T淋巴细胞在癌症发展中的作用以及潜在的细胞和分子机制的现有知识。