| Literature DB >> 32042052 |
Yutaka Nakamura1,2, Hitomi Mimuro3,4, Jun Kunisawa5,6, Yukihiro Furusawa1,7, Daisuke Takahashi1, Yumiko Fujimura1, Tsuneyasu Kaisho8, Hiroshi Kiyono5,9,10,11, Koji Hase12,13.
Abstract
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.Entities:
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Year: 2020 PMID: 32042052 DOI: 10.1038/s41385-020-0263-0
Source DB: PubMed Journal: Mucosal Immunol ISSN: 1933-0219 Impact factor: 7.313