Division of Biochemistry, Faculty of Pharmacy and Graduate School of Pharmaceutical Science, Keio University, Tokyo, 105-0011, Japan.
Graduate School of Medicine, The University of Tokyo, Tokyo, 113-0033, Japan.
Mucosal Immunol. 2020 Jul;13(4):679-690. doi: 10.1038/s41385-020-0263-0. Epub 2020 Feb 10.
Infectious colitis is one of the most common health issues worldwide. Microfold (M) cells actively transport luminal antigens to gut-associated lymphoid tissue to induce IgA responses; however, it remains unknown whether M cells contribute to the induction of cellular immune responses. Here we report that M cell-dependent antigen transport plays a critical role in the induction of Th1, Th17, and Th22 responses against gut commensals in the steady state. The establishment of commensal-specific cellular immunity was a prerequisite for preventing bacterial dissemination during enteropathogenic Citrobacter rodentium infection. Therefore, M cell-null mice developed severe colitis with increased bacterial dissemination. This abnormality was associated with mucosal barrier dysfunction. These observations suggest that antigen transport by M cells may help maintain gut immune homeostasis by eliciting antigen-specific cellular immune responses.
传染性结肠炎是全球最常见的健康问题之一。微褶皱(M)细胞主动将腔抗原转运至肠相关淋巴组织,以诱导 IgA 反应;然而,目前尚不清楚 M 细胞是否有助于诱导细胞免疫反应。在这里,我们报告 M 细胞依赖性抗原转运在稳定状态下诱导针对肠道共生菌的 Th1、Th17 和 Th22 反应中起着关键作用。共生菌特异性细胞免疫的建立是防止肠道致病性柠檬酸杆菌感染期间细菌扩散的前提条件。因此,M 细胞缺陷小鼠发生严重结肠炎伴细菌播散增加。这种异常与粘膜屏障功能障碍有关。这些观察结果表明,M 细胞的抗原转运可能通过引发抗原特异性细胞免疫反应来帮助维持肠道免疫稳态。