Aire regulates negative selection of organ-specific T cells
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Liston, A
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Lesage, S
Wilson, J
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机构:Australian Natl Univ, John Curtin Sch Med Res, Med Genome Ctr, ACRF Genet Lab, Canberra, ACT 2601, Australia
Wilson, J
Peltonen, L
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机构:Australian Natl Univ, John Curtin Sch Med Res, Med Genome Ctr, ACRF Genet Lab, Canberra, ACT 2601, Australia
Peltonen, L
Goodnow, CC
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Australian Natl Univ, John Curtin Sch Med Res, Med Genome Ctr, ACRF Genet Lab, Canberra, ACT 2601, AustraliaAustralian Natl Univ, John Curtin Sch Med Res, Med Genome Ctr, ACRF Genet Lab, Canberra, ACT 2601, Australia
Goodnow, CC
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[1] Australian Natl Univ, John Curtin Sch Med Res, Med Genome Ctr, ACRF Genet Lab, Canberra, ACT 2601, Australia
[2] Univ Helsinki, Dept Med Genet & Mol Med, FIN-00014 Helsinki, Finland
Autoimmune polyendocrinopathy syndrome type 1 is a recessive Mendelian disorder resulting from mutations in a novel gene, AIRE, and is characterized by a spectrum of organ-specific autoimmune diseases. It is not known what tolerance mechanisms are defective as a result of AIRE mutation. By tracing the fate of autoreactive CD4(+) T cells with high affinity for a pancreatic antigen in transgenic mice with an Aire mutation, we show here that Aire deficiency causes almost complete failure to delete the organ-specific cells in the thymus. These results indicate that autoimmune polyendocrinopathy syndrome I is caused by failure of a specialized mechanism for deleting forbidden T cell clones, establishing a central role for this tolerance mechanism.