Murugaiyan Gopal, Mittal Akanksha, Lopez-Diego Rocio, Maier Lisa M, Anderson David E, Weiner Howard L
Center for Neurologic Diseases, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
J Immunol. 2009 Aug 15;183(4):2435-43. doi: 10.4049/jimmunol.0900568. Epub 2009 Jul 22.
Although the physiologic pathways that control regulatory T cells (Foxp3-expressing regulatory T cells, IL-10-secreting Tr1 cells) and Th17 cells in rodents have been defined, the factors that control these differentiation pathways in humans are not well understood. In this study, we show that IL-27 promotes the differentiation of IL-10-secreting Tr1 cells while inhibiting Th17 generation and molecules associated with Th17 function. Furthermore, IL-27 inhibits IL-17-polarizing cytokines on dendritic cells, which in turn decrease IL-17 secretion from T cells. Our results demonstrate that IL-27 plays a key role in human T cells by promoting IL-10-secreting Tr1 cells and inhibiting Th17 cells and thus provides a dual regulatory mechanism to control autoimmunity and tissue inflammation.
虽然在啮齿动物中控制调节性T细胞(表达Foxp3的调节性T细胞、分泌IL-10的Tr1细胞)和Th17细胞的生理途径已被明确,但控制人类这些分化途径的因素尚未完全了解。在本研究中,我们发现IL-27促进分泌IL-10的Tr1细胞的分化,同时抑制Th17细胞的生成以及与Th17功能相关的分子。此外,IL-27抑制树突状细胞上的IL-17极化细胞因子,进而减少T细胞分泌IL-17。我们的结果表明,IL-27通过促进分泌IL-10的Tr1细胞和抑制Th17细胞,在人类T细胞中发挥关键作用,从而提供了一种双重调节机制来控制自身免疫和组织炎症。