Fine tuning subsets of CD4+ T cells by low-dosage of IL-2 and a new therapeutic strategy for autoimmune diseases

Int Immunopharmacol. 2018 Mar:56:269-276. doi: 10.1016/j.intimp.2018.01.042. Epub 2018 Feb 3.

Abstract

Although Interleukin-2 (IL-2) was identified almost 40 years ago, only recently low dosage IL-2 therapy is proved to be an effective approach to treat autoimmune diseases. The underlining mechanism is that IL-2 can fine-tune subsets of CD4+ T cells by promoting the development and maintenance of regulatory T cells (Treg) at low-dosage (ld) and enhance the functions of effector T cells (Teff) at high-dosage (hd). Since the successful clinical trials of IL-2 to treat patients with autoimmune diseases and inflammatory conditions, including Systemic lupus erythematosus (SLE) and Type 1 Diabetes (T1D), ld IL-2 therapy is a promising strategy to treat autoimmune diseases.

Keywords: Autoimmune diseases; Effector T cells; IL-2; Regulatory T cells.

Publication types

  • Review

MeSH terms

  • Animals
  • Autoimmune Diseases / immunology
  • Autoimmune Diseases / therapy*
  • CD4 Antigens / metabolism
  • Homeostasis
  • Humans
  • Immune Tolerance
  • Immunomodulation
  • Immunotherapy / methods*
  • Interleukin-2 / therapeutic use*
  • Lymphocyte Activation
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocytes, Regulatory / immunology*

Substances

  • CD4 Antigens
  • Interleukin-2