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

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 a...

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Veröffentlicht in:Human molecular genetics 2002-02, Vol.11 (4), p.397-409
Hauptverfasser: Ramsey, Chris, Winqvist, Ola, Puhakka, Lea, Halonen, Maria, Moro, Aune, Kämpe, Olle, Eskelin, Petra, Pelto-Huikko, Markku, Peltonen, Leena
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Sprache:eng
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Zusammenfassung: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.
ISSN:0964-6906
1460-2083
DOI:10.1093/hmg/11.4.397