FOXP3+ regulatory T cells and age-related diseases

FEBS J. 2022 Jan;289(2):319-335. doi: 10.1111/febs.15743. Epub 2021 Feb 18.

Abstract

Regulatory T (Treg) cells are critical for the maintenance of immune homeostasis. Dysregulation of Treg cells has been implicated in the pathogenesis of autoimmunity and chronic inflammation, while aging is characterized by an accumulation of inflammatory markers in the peripheral blood, a phenomenon known as 'inflammaging'. The relationship between Treg cells and age-related diseases remains to be further studied. Increasing evidence revealed that Treg cells' dysfunction occurs in aged patients, suggesting that immune therapies targeting Treg cells may be a promising approach to treat diseases such as cancers and autoimmune diseases. Furthermore, drugs targeting Treg cells show encouraging results and contribute to CD8+ T-cell-mediated cytotoxic killing of tumor and infected cells. In general, a better understanding of Treg cell function may help us to develop new immune therapies against aging. In this review, we discuss potential therapeutic strategies to modify immune responses of relevance for aging to prevent and treat age-related diseases, as well as the challenges posed by the translation of novel immune therapies into clinical practice.

Keywords: Treg-based immune therapy; age-related diseases; regulatory T cells.

Publication types

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

MeSH terms

  • Aging / immunology*
  • Aging / pathology
  • Autoimmune Diseases / immunology
  • Autoimmune Diseases / therapy
  • CD8-Positive T-Lymphocytes / immunology
  • Forkhead Transcription Factors / genetics*
  • Forkhead Transcription Factors / immunology
  • Homeostasis / immunology
  • Humans
  • Immunity / genetics
  • Immunity / immunology*
  • Inflammation / immunology
  • Inflammation / therapy
  • Leukocytes, Mononuclear / immunology
  • Neoplasms / immunology
  • Neoplasms / therapy
  • T-Lymphocytes, Regulatory / immunology*

Substances

  • FOXP3 protein, human
  • Forkhead Transcription Factors