O'Brien Rebecca L, Born Willi K
Department of Biomedical Research, National Jewish Health, Denver, CO, USA.
Department of Immunology and Microbiology, University of Colorado Denver School of Medicine, Aurora, CO, USA.
Immunol Rev. 2020 Nov;298(1):10-24. doi: 10.1111/imr.12905. Epub 2020 Jul 22.
The γδ T cells play an important role in both mice and humans as a source of the cytokine IL-17, which is key for immune resistance to certain pathogens. In mice, most of these IL-17 producers, termed γδT-17 cells, actually comprise two distinct types: those expressing an invariant Vγ6Vδ1 TCR and those expressing a Vγ4 TCR. Murine γδT-17 cells acquire an inherent bias to produce IL-17 and other "type 17" cytokines during thymic development. The similarities and differences between the two mouse γδT-17 types are reviewed here, and the potential implications of their differences are discussed. There is some evidence that two distinct TCR-defined IL-17-producing γδ T cell subsets also exist in humans, but unlike the mouse γδT-17 cells, these cells are probably not imprinted with an IL-17 bias during thymic development, but rather acquire an IL-17 bias in the periphery.
γδ T细胞在小鼠和人类中均作为细胞因子IL-17的来源发挥重要作用,IL-17是对某些病原体产生免疫抵抗的关键因素。在小鼠中,这些产生IL-17的细胞(称为γδT-17细胞)大多数实际上包含两种不同类型:表达恒定Vγ6Vδ1 TCR的细胞和表达Vγ4 TCR的细胞。小鼠γδT-17细胞在胸腺发育过程中获得产生IL-17和其他“17型”细胞因子的内在倾向。本文综述了两种小鼠γδT-17细胞类型之间的异同,并讨论了它们差异的潜在影响。有证据表明,人类中也存在两个由TCR定义的不同的产生IL-17的γδ T细胞亚群,但与小鼠γδT-17细胞不同,这些细胞在胸腺发育过程中可能没有被赋予产生IL-17的倾向,而是在外周获得了产生IL-17的倾向。