Teng Fei, Klinger Christina N, Felix Krysta M, Bradley C Pierce, Wu Eric, Tran Nhan L, Umesaki Yoshinori, Wu Hsin-Jung Joyce
Department of Immunobiology, University of Arizona, Tucson, AZ 85719, USA.
Yakult Central Institute, Izumi 5-11, Kunitachi, Tokyo, Japan.
Immunity. 2016 Apr 19;44(4):875-88. doi: 10.1016/j.immuni.2016.03.013.
Gut microbiota profoundly affect gut and systemic diseases, but the mechanism whereby microbiota affect systemic diseases is unclear. It is not known whether specific microbiota regulate T follicular helper (Tfh) cells, whose excessive responses can inflict antibody-mediated autoimmunity. Using the K/BxN autoimmune arthritis model, we demonstrated that Peyer's patch (PP) Tfh cells were essential for gut commensal segmented filamentous bacteria (SFB)-induced systemic arthritis despite the production of auto-antibodies predominantly occurring in systemic lymphoid tissues, not PPs. We determined that SFB, by driving differentiation and egress of PP Tfh cells into systemic sites, boosted systemic Tfh cell and auto-antibody responses that exacerbated arthritis. SFB induced PP Tfh cell differentiation by limiting the access of interleukin 2 to CD4(+) T cells, thereby enhancing Tfh cell master regulator Bcl-6 in a dendritic cell-dependent manner. These findings showed that gut microbiota remotely regulated a systemic disease by driving the induction and egress of gut Tfh cells.
肠道微生物群对肠道和全身性疾病有深远影响,但微生物群影响全身性疾病的机制尚不清楚。目前尚不清楚特定的微生物群是否调节滤泡辅助性T细胞(Tfh),其过度反应可导致抗体介导的自身免疫。利用K/BxN自身免疫性关节炎模型,我们证明,尽管自身抗体的产生主要发生在全身淋巴组织而非派尔集合淋巴结(PP),但PP中的Tfh细胞对于肠道共生分节丝状菌(SFB)诱导的全身性关节炎至关重要。我们确定,SFB通过驱动PP Tfh细胞向全身部位的分化和迁移,增强了全身性Tfh细胞和自身抗体反应,从而加剧了关节炎。SFB通过限制白细胞介素2与CD4(+) T细胞的接触来诱导PP Tfh细胞分化,从而以树突状细胞依赖的方式增强Tfh细胞主调节因子Bcl-6。这些发现表明,肠道微生物群通过驱动肠道Tfh细胞的诱导和迁移来远程调节全身性疾病。