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

被引:356
作者
Ramsey, C
Winqvist, O
Puhakka, L
Halonen, M
Moro, A
Kämpe, O
Eskelin, P
Pelto-Huikko, M
Peltonen, L
机构
[1] Univ Calif Los Angeles, Sch Med, Gonda Ctr, Dept Human Genet, Los Angeles, CA 90095 USA
[2] Univ Uppsala Hosp, Dept Internal Med, S-75185 Uppsala, Sweden
[3] Natl Publ Hlth Inst, Dept Human Mol Genet, Helsinki, Finland
[4] Univ Helsinki Hosp, Hosp Children & Adolescence, Helsinki, Finland
[5] Tampere Univ, Sch Med, Dept Dev Biol & Pathol, FIN-33101 Tampere, Finland
[6] Tampere Univ Hosp, Tampere, Finland
[7] Univ Helsinki, Dept Med Genet, Helsinki, Finland
关键词
D O I
10.1093/hmg/11.4.397
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:397 / 409
页数:13
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