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自身免疫调节因子突变与自身免疫性疾病

AIRE-mutations and autoimmune disease.

作者信息

Bruserud Øyvind, Oftedal Bergithe E, Wolff Anette B, Husebye Eystein S

机构信息

Department of Clinical Science, University of Bergen, 5021 Bergen, Norway.

Department of Clinical Science, University of Bergen, 5021 Bergen, Norway; Department of Medicine, Haukeland University Hospital, 5021 Bergen, Norway.

出版信息

Curr Opin Immunol. 2016 Dec;43:8-15. doi: 10.1016/j.coi.2016.07.003. Epub 2016 Aug 6.

Abstract

The gene causing the severe organ-specific autoimmune disease autoimmune polyendocrine syndrome type-1 (APS-1) was identified in 1997 and named autoimmune regulator (AIRE). AIRE plays a key role in shaping central immunological tolerance by facilitating negative selection of T cells in the thymus, building the thymic microarchitecture, and inducing a specific subset of regulatory T cells. So far, about 100 mutations have been identified. Recent advances suggest that certain mutations located in the SAND and PHD1 domains exert a dominant negative effect on wild type AIRE resulting in milder seemingly common forms of autoimmune diseases, including pernicious anemia, vitiligo and autoimmune thyroid disease. These findings indicate that AIRE also contribute to autoimmunity in more common organ-specific autoimmune disorders.

摘要

导致严重器官特异性自身免疫性疾病1型自身免疫性多内分泌综合征(APS-1)的基因于1997年被鉴定出来,并命名为自身免疫调节因子(AIRE)。AIRE通过促进胸腺中T细胞的阴性选择、构建胸腺微结构以及诱导特定亚群的调节性T细胞,在塑造中枢免疫耐受方面发挥关键作用。到目前为止,已鉴定出约100种突变。最近的研究进展表明,位于SAND和PHD1结构域的某些突变对野生型AIRE产生显性负效应,导致出现较为温和的看似常见的自身免疫性疾病形式,包括恶性贫血、白癜风和自身免疫性甲状腺疾病。这些发现表明,AIRE在更常见的器官特异性自身免疫性疾病中也与自身免疫有关。

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