Increased antigen presenting cell-mediated T cell activation in mice and patients without the autoimmune regulator

Eur J Immunol. 2006 Feb;36(2):305-17. doi: 10.1002/eji.200535240.

Abstract

Patients with autoimmune polyendocrine syndrome type I (APS I)suffer from endocrine and non-endocrine disorders due to mutations in the autoimmune regulator gene (AIRE). Mouse Aire is expressed both in thymic medullary epithelial cells and in peripheral antigen-presenting cells, suggesting a role in both central and peripheral tolerance. We here report that Aire(-/-) dendritic cells (DC) activate naive T cells more efficiently than do Aire(+/+) DC. Expression array analyses of Aire(-/-) DC revealed differential regulation of 68 transcripts, among which, the vascular cell adhesion molecule-1 (VCAM-1) transcript was up-regulated in Aire(-/-) DC. Concurrently, the expression of the VCAM-1 protein was up-regulated on both Aire(-/-) DC and monocytes from APS I patients. Blocking the interaction of VCAM-1 prevented enhanced Aire(-/-) DC stimulation of T cell hybridomas. We determined an increased number of DC in spleen and lymph nodes and of monocytes in the blood from Aire(-/-) mice, and an increased number of blood monocytes in APS I patients. Our findings imply a role for Aire in peripheral DC regulation of T cell activation, and suggest that Aire participates in peripheral tolerance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AIRE Protein
  • Animals
  • Antigen Presentation / genetics
  • Antigen Presentation / immunology
  • Autoimmune Diseases / genetics
  • Autoimmune Diseases / immunology*
  • Autoimmune Diseases / pathology
  • Cell Adhesion / genetics
  • Cell Adhesion / immunology
  • Dendritic Cells / immunology
  • Dendritic Cells / pathology
  • Endocrine System Diseases / genetics
  • Endocrine System Diseases / immunology*
  • Endocrine System Diseases / pathology
  • Epithelial Cells / immunology
  • Epithelial Cells / pathology
  • Humans
  • Immune Tolerance / genetics
  • Immune Tolerance / immunology*
  • Lymphocyte Activation / genetics
  • Lymphocyte Activation / immunology*
  • Mice
  • Mice, Knockout
  • Monocytes / immunology
  • Monocytes / pathology
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / pathology
  • Thymus Gland / immunology
  • Thymus Gland / pathology
  • Transcription Factors / deficiency*
  • Transcription Factors / immunology
  • Up-Regulation / genetics
  • Up-Regulation / immunology
  • Vascular Cell Adhesion Molecule-1 / genetics
  • Vascular Cell Adhesion Molecule-1 / immunology

Substances

  • Transcription Factors
  • Vascular Cell Adhesion Molecule-1