Insulin-like growth factor 2 enhances regulatory T-cell functions and suppresses food allergy in an experimental model

J Allergy Clin Immunol. 2014 Jun;133(6):1702-8.e5. doi: 10.1016/j.jaci.2014.02.019. Epub 2014 Apr 1.

Abstract

Background: The functions of regulatory T (Treg) cells are important in immunity, and the regulatory mechanisms of Treg cell activities are not fully understood yet.

Objectives: We sought to investigate the role of insulin-like growth factor (IGF) 2 in the upregulation of Treg cell function.

Methods: The expression of insulin-like growth factor 2 receptor (IGF2R) on T cells was assessed by using flow cytometry. Treg cell functions were evaluated by assessing the suppressor effect on proliferation of other effector T (Teff) cells. The effect of IGF2 on regulating Treg cell functions were evaluated with a cell-culture model and a food allergy mouse model.

Results: Expression of IGF2R was observed in more than 90% of murine and human Treg cells but in less than 10% of effector CD4(+) T cells. Activation of IGF2R and T-cell receptor induced marked Treg cell proliferation and release of TGF-β from Treg cells, which enhanced Treg cell immune suppressor effects on other Teff cell activities and allergic inflammation in the intestine.

Conclusions: Activation of IGF2R enhances Treg cell functions in suppressing other Teff cell activities and inhibiting allergic inflammation in the intestine.

Keywords: Regulatory T cell; allergy; insulin-like growth factor; intestine; transforming growth factor.

Publication types

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

MeSH terms

  • Adoptive Transfer
  • Adult
  • Animals
  • Disease Models, Animal
  • Female
  • Food Hypersensitivity / genetics
  • Food Hypersensitivity / immunology*
  • Food Hypersensitivity / metabolism*
  • Forkhead Transcription Factors / metabolism
  • Gene Expression
  • Gene Silencing
  • Humans
  • Immunophenotyping
  • Insulin-Like Growth Factor II / metabolism*
  • Intestinal Mucosa / metabolism
  • Intestines / immunology
  • Intestines / pathology
  • Lymphocyte Activation / immunology
  • Male
  • Mice
  • Phenotype
  • Receptor, IGF Type 2 / genetics
  • Receptor, IGF Type 2 / metabolism
  • T-Lymphocytes, Regulatory / immunology*
  • T-Lymphocytes, Regulatory / metabolism*
  • Young Adult

Substances

  • Forkhead Transcription Factors
  • Receptor, IGF Type 2
  • Insulin-Like Growth Factor II