Helminth protection against type-1 diabetes: an insight into immunomodulatory effect of helminth-induced infection

Mol Biol Rep. 2021 Sep;48(9):6581-6588. doi: 10.1007/s11033-021-06663-9. Epub 2021 Aug 25.

Abstract

Helminths are the old dirty friends of humans from decades and may live undetected by the immune system for years in the tissues. They have evolved as good experts at subverting the immune system. Despite of their pathogenicity, they provide protection to their host against certain inflammatory diseases such as diabetes by modulating the immune mechanisms. These parasites are extra-cellular and induce Th2 response which triggers the adaptive immune cells as well as innate immune cells to work synergistically allowing Tregs to work in a toll-like receptor-dependent manure. T-helper cells type-2 also secrete certain anti-inflammatory cytokines including IL-4, IL-10, IL-13 and TGF-β which also provide protection against type-1 diabetes. Several helminths such as T. crassiceps, S. venezuelensis, filarial worms, Schistosoma spp. and T. spiralis have been reported to prevent diabetes in mouse models as well as in some clinical trials. Immunomodulatory talent of helminths is receiving greater attention to prevent diabetes. Herein, an attempt has been made to review and highlight the possible immuno-modulatory mechanisms by which helminths provide protection against diabetes. Moreover, this review also emphasizes on the use of helminth-derived molecules or synthetic derivatives of helminth-antigens in clinical trials to overcome rapidly growing autoimmune disorders including diabetes.

Keywords: Autoimmunity; Diabetes; Helminths; Immuno-modulation; Tregs.

Publication types

  • Review

MeSH terms

  • Adaptive Immunity*
  • Animals
  • Antigens, Helminth / immunology
  • Cytokines / metabolism
  • Diabetes Mellitus, Type 1 / immunology*
  • Diabetes Mellitus, Type 1 / prevention & control*
  • Disease Models, Animal
  • Helminthiasis / immunology*
  • Helminthiasis / parasitology
  • Helminths / immunology*
  • Humans
  • Immunity, Innate*
  • Mice
  • T-Lymphocytes, Regulatory / immunology
  • Th2 Cells / immunology

Substances

  • Antigens, Helminth
  • Cytokines