Aire deficient mice develop multiple features of APECED phenotype and show altered immune response

Hum Mol Genet. 2002 Feb 15;11(4):397-409. doi: 10.1093/hmg/11.4.397.

Abstract

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is a monogenic autosomal recessive disease caused by mutations in the AIRE gene. Here we have produced knock-out mice for the Aire gene. The Aire-/- mice develop normally; however, autoimmune features of APECED in Aire-/- mice are evident, including multiorgan lymphocytic infiltration, circulating autoantibodies and infertility. The distribution of B and T cells and thymic maturation as well as activation of T cells appear normal, while the TCR-Vbeta repertoire is altered in peripheral T cells of Aire-/- mice. When mice are challenged with immunization, the peripheral T cells of Aire-/- mice have a 3-5-fold increased proliferation. These findings suggest that the Aire gene is not necessary for normal T cell education and development, while a defect in immune response detected in challenged Aire-/- mice underlines the crucial role of AIRE/Aire in maintaining homeostatic regulation in the immune system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AIRE Protein
  • Animals
  • Autoantibodies / blood
  • Autoantibodies / immunology
  • CD4-CD8 Ratio
  • Disease Models, Animal
  • Gene Targeting
  • Infertility / genetics
  • Mice
  • Mice, Knockout
  • Polyendocrinopathies, Autoimmune / genetics*
  • Polyendocrinopathies, Autoimmune / immunology
  • Polyendocrinopathies, Autoimmune / pathology
  • T-Lymphocytes / immunology
  • T-Lymphocytes / physiology
  • Transcription Factors / genetics*
  • Transcription Factors / immunology
  • Transcription Factors / physiology

Substances

  • Autoantibodies
  • Transcription Factors