Dutzan Nicolas, Abusleme Loreto, Bridgeman Hayley, Greenwell-Wild Teresa, Zangerle-Murray Tamsin, Fife Mark E, Bouladoux Nicolas, Linley Holly, Brenchley Laurie, Wemyss Kelly, Calderon Gloria, Hong Bo-Young, Break Timothy J, Bowdish Dawn M E, Lionakis Michail S, Jones Simon A, Trinchieri Giorgio, Diaz Patricia I, Belkaid Yasmine, Konkel Joanne E, Moutsopoulos Niki M
Oral Immunity and Inflammation Unit, NIDCR, NIH, Bethesda, MD 20892, USA.
Faculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, UK; Manchester Collaborative Centre for Inflammation Research (MCCIR), University of Manchester, Manchester M13 9NT, UK.
Immunity. 2017 Jan 17;46(1):133-147. doi: 10.1016/j.immuni.2016.12.010. Epub 2017 Jan 10.
Immuno-surveillance networks operating at barrier sites are tuned by local tissue cues to ensure effective immunity. Site-specific commensal bacteria provide key signals ensuring host defense in the skin and gut. However, how the oral microbiome and tissue-specific signals balance immunity and regulation at the gingiva, a key oral barrier, remains minimally explored. In contrast to the skin and gut, we demonstrate that gingiva-resident T helper 17 (Th17) cells developed via a commensal colonization-independent mechanism. Accumulation of Th17 cells at the gingiva was driven in response to the physiological barrier damage that occurs during mastication. Physiological mechanical damage, via induction of interleukin 6 (IL-6) from epithelial cells, tailored effector T cell function, promoting increases in gingival Th17 cell numbers. These data highlight that diverse tissue-specific mechanisms govern education of Th17 cell responses and demonstrate that mechanical damage helps define the immune tone of this important oral barrier.
在屏障部位运作的免疫监视网络会根据局部组织信号进行调节,以确保有效的免疫反应。特定部位的共生细菌提供关键信号,确保皮肤和肠道中的宿主防御。然而,在牙龈这一关键的口腔屏障部位,口腔微生物群和组织特异性信号如何平衡免疫和调节作用,仍鲜有人探索。与皮肤和肠道不同,我们证明牙龈驻留的辅助性T细胞17(Th17)细胞是通过一种不依赖共生菌定植的机制发育而来的。牙龈处Th17细胞的积累是对咀嚼过程中发生的生理性屏障损伤作出的反应。生理性机械损伤通过诱导上皮细胞产生白细胞介素6(IL-6),调整效应T细胞功能,促进牙龈Th17细胞数量增加。这些数据表明,多种组织特异性机制调控Th17细胞反应的形成,并证明机械损伤有助于确定这一重要口腔屏障的免疫状态。