Microfold cell-dependent antigen transport alleviates infectious colitis by inducing antigen-specific cellular immunity

Mucosal Immunol. 2020 Jul;13(4):679-690. doi: 10.1038/s41385-020-0263-0. Epub 2020 Feb 10.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens / immunology*
  • Antigens / metabolism*
  • Colitis / etiology*
  • Colitis / metabolism*
  • Colitis / pathology
  • Disease Models, Animal
  • Disease Susceptibility
  • Gastrointestinal Microbiome / immunology
  • Host-Pathogen Interactions / immunology
  • Immunity, Cellular*
  • Immunity, Mucosal*
  • Immunoglobulin A / immunology
  • Intestinal Mucosa / cytology
  • Intestinal Mucosa / immunology*
  • Intestinal Mucosa / metabolism*
  • Mice
  • Mice, Knockout
  • Organ Specificity / immunology
  • Peyer's Patches / immunology
  • Peyer's Patches / metabolism
  • T-Lymphocytes, Helper-Inducer / immunology
  • T-Lymphocytes, Helper-Inducer / metabolism

Substances

  • Antigens
  • Immunoglobulin A