ICOS+ Tregs: A Functional Subset of Tregs in Immune Diseases

Front Immunol. 2020 Aug 28:11:2104. doi: 10.3389/fimmu.2020.02104. eCollection 2020.

Abstract

Recent studies have reported the pathological effect of ICOS+ T cells, but ICOS signals also widely participate in anti-inflammatory responses, particularly ICOS+ regulatory T (Treg) cells. The ICOS signaling pathway endows Tregs with increased generation, proliferation, and survival abilities. Furthermore, there is enough evidence to suggest a superior capacity of ICOS+ Tregs, which is partly attributable to IL-10 induced by ICOS, yet the associated mechanism needs further investigation. In this review, we discuss the complicated role of ICOS+ Tregs in several classical autoimmune diseases, allergic diseases, and cancers and investigate the related therapeutic applications in these diseases. Moreover, we identify ICOS as a potential biomarker for disease treatment and prognostic prediction. In addition, we believe that anti-ICOS/ICOSL monoclonal antibodies exhibit excellent clinical application potential. A thorough understanding of the effect of ICOS+ Tregs and the holistic role of ICOS toward the immune system will help to improve the therapeutic schedule of diseases.

Keywords: ICOS; Treg cells; autoimmune disease; immunotherapy; neoplasm.

Publication types

  • Review

MeSH terms

  • Animals
  • Autoimmune Diseases / immunology*
  • Autoimmune Diseases / pathology
  • Autoimmune Diseases / therapy
  • Biomarkers
  • Humans
  • Inducible T-Cell Co-Stimulator Protein / immunology*
  • Interleukin-10 / immunology
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / pathology

Substances

  • Biomarkers
  • ICOS protein, human
  • IL10 protein, human
  • Inducible T-Cell Co-Stimulator Protein
  • Interleukin-10