Worthington John J, Kelly Aoife, Smedley Catherine, Bauché David, Campbell Simon, Marie Julien C, Travis Mark A
Manchester Collaborative Centre for Inflammation Research, University of Manchester, Manchester M13 9NT, UK; Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester M13 9PT, UK; Manchester Immunology Group, Faculty of Life Sciences, University of Manchester, Manchester M13 9PT, UK.
Manchester Collaborative Centre for Inflammation Research, University of Manchester, Manchester M13 9NT, UK; Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester M13 9PT, UK; Manchester Immunology Group, Faculty of Life Sciences, University of Manchester, Manchester M13 9PT, UK.
Immunity. 2015 May 19;42(5):903-15. doi: 10.1016/j.immuni.2015.04.012. Epub 2015 May 12.
Regulatory T (Treg) cells play a pivotal role in suppressing self-harmful T cell responses, but how Treg cells mediate suppression to maintain immune homeostasis and limit responses during inflammation is unclear. Here we show that effector Treg cells express high amounts of the integrin αvβ8, which enables them to activate latent transforming growth factor-β (TGF-β). Treg-cell-specific deletion of integrin αvβ8 did not result in a spontaneous inflammatory phenotype, suggesting that this pathway is not important in Treg-cell-mediated maintenance of immune homeostasis. However, Treg cells lacking expression of integrin αvβ8 were unable to suppress pathogenic T cell responses during active inflammation. Thus, our results identify a mechanism by which Treg cells suppress exuberant immune responses, highlighting a key role for effector Treg-cell-mediated activation of latent TGF-β in suppression of self-harmful T cell responses during active inflammation.
调节性T(Treg)细胞在抑制自身有害的T细胞反应中起关键作用,但Treg细胞如何介导抑制作用以维持免疫稳态并在炎症期间限制反应尚不清楚。在这里,我们表明效应Treg细胞表达大量整合素αvβ8,这使它们能够激活潜伏的转化生长因子-β(TGF-β)。整合素αvβ8的Treg细胞特异性缺失并未导致自发炎症表型,这表明该途径在Treg细胞介导的免疫稳态维持中并不重要。然而,缺乏整合素αvβ8表达的Treg细胞在活动性炎症期间无法抑制致病性T细胞反应。因此,我们的结果确定了一种Treg细胞抑制过度免疫反应的机制,突出了效应Treg细胞介导的潜伏TGF-β激活在活动性炎症期间抑制自身有害T细胞反应中的关键作用。