The Many Functions of Foxp3+ Regulatory T Cells in the Intestine

Front Immunol. 2020 Oct 20:11:600973. doi: 10.3389/fimmu.2020.600973. eCollection 2020.

Abstract

Throughout the last years, gut-resident Foxp3+ regulatory T (Treg) cells have been associated with a growing number of tissue-specific functions in the intestine, comprising various aspects of gut immunity and physiology. Treg cells have pivotal roles in intestinal tolerance induction and host defense by actively controlling immune responses towards harmless dietary antigens and commensal microorganisms as well as towards invading pathogens. In addition to these immune-related roles, it has become increasingly clear that intestinal Treg cells also exert important non-immune functions in the gut, such as promoting local tissue repair and preserving the integrity of the epithelial barrier. Thereby, intestinal Treg cells critically contribute to the maintenance of tissue homeostasis. In order to account for this functional diversity, gut-resident Treg cells have specifically adapted to the intestinal tissue microenvironment. In this Review, we discuss the specialization of Treg cells in the intestine. We survey the different populations of gut-resident Treg cells focussing on their unique functions, phenotypes and distinct transcription factor dependencies.

Keywords: Treg cell; diet; functions; intestinal epithelial cells; intestinal tolerance; microbiota; phenotypes; tissue homeostasis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Bacteria / immunology
  • Bacteria / pathogenicity
  • Cellular Microenvironment
  • Forkhead Transcription Factors / metabolism*
  • Gastrointestinal Microbiome
  • Host-Pathogen Interactions
  • Humans
  • Immune Tolerance
  • Immunity, Mucosal*
  • Inflammatory Bowel Diseases / immunology
  • Inflammatory Bowel Diseases / metabolism
  • Inflammatory Bowel Diseases / microbiology
  • Intestinal Mucosa / immunology*
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / microbiology
  • Phenotype
  • Signal Transduction
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / metabolism
  • T-Lymphocytes, Regulatory / microbiology

Substances

  • FOXP3 protein, human
  • Forkhead Transcription Factors