Tissue Resident Foxp3+ Regulatory T Cells: Sentinels and Saboteurs in Health and Disease

Juyeun Lee, Dongkyun Kim, Booki Min*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

16 Scopus citations

Abstract

Foxp3+ regulatory T (Treg) cells are a CD4 T cell subset with unique immune regulatory function that are indispensable in immunity and tolerance. Their indisputable importance has been investigated in numerous disease settings and experimental models. Despite the extensive efforts in determining the cellular and molecular mechanisms operating their functions, our understanding their biology especially in vivo remains limited. There is emerging evidence that Treg cells resident in the non-lymphoid tissues play a central role in regulating tissue homeostasis, inflammation, and repair. Furthermore, tissue-specific properties of those Treg cells that allow them to express tissue specific functions have been explored. In this review, we will discuss the potential mechanisms and key cellular/molecular factors responsible for the homeostasis and functions of tissue resident Treg cells under steady-state and inflammatory conditions.

Original languageEnglish (US)
Article number865593
JournalFrontiers in immunology
Volume13
DOIs
StatePublished - Mar 11 2022

Funding

This work was supported by NIH grant AI125247 and NMSS grant RG1806-31374 (BM).

Keywords

  • Foxp3
  • homeostasis
  • inflammation
  • regulatory T cell
  • tissue residency

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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