Aire regulates the transfer of antigen from mTECs to dendritic cells for induction of thymic tolerance

Blood. 2011 Sep 1;118(9):2462-72. doi: 10.1182/blood-2010-06-286393. Epub 2011 Apr 19.

Abstract

To investigate the role of Aire in thymic selection, we examined the cellular requirements for generation of ovalbumin (OVA)-specific CD4 and CD8 T cells in mice expressing OVA under the control of the rat insulin promoter. Aire deficiency reduced the number of mature single-positive OVA-specific CD4(+) or CD8(+) T cells in the thymus, independent of OVA expression. Importantly, it also contributed in 2 ways to OVA-dependent negative selection depending on the T-cell type. Aire-dependent negative selection of OVA-specific CD8 T cells correlated with Aire-regulated expression of OVA. By contrast, for OVA-specific CD4 T cells, Aire affected tolerance induction by a mechanism that operated independent of the level of OVA expression, controlling access of antigen presenting cells to medullary thymic epithelial cell (mTEC)-expressed OVA. This study supports the view that one mechanism by which Aire controls thymic negative selection is by regulating the indirect presentation of mTEC-derived antigens by thymic dendritic cells. It also indicates that mTECs can mediate tolerance by direct presentation of Aire-regulated antigens to both CD4 and CD8 T cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AIRE Protein
  • Animals
  • Antigen Presentation*
  • Antigens / immunology
  • Antigens / metabolism*
  • Bone Marrow Transplantation
  • CD4-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / immunology
  • Clonal Deletion / immunology*
  • Crosses, Genetic
  • Cytokines / metabolism
  • Dendritic Cells / immunology*
  • Epithelial Cells / immunology*
  • Gene Expression Regulation / immunology
  • Immune Tolerance / immunology*
  • Insulin / genetics
  • Mice
  • Mice, Transgenic
  • Ovalbumin / genetics
  • Ovalbumin / immunology
  • Ovalbumin / metabolism
  • Promoter Regions, Genetic
  • Radiation Chimera
  • Recombinant Fusion Proteins / physiology
  • Thymus Gland / cytology
  • Thymus Gland / immunology*
  • Transcription Factors / deficiency
  • Transcription Factors / genetics
  • Transcription Factors / immunology*

Substances

  • Antigens
  • Cytokines
  • Insulin
  • Recombinant Fusion Proteins
  • Transcription Factors
  • Ovalbumin