Autoimmune regulator and self-tolerance - molecular and clinical aspects

被引:72
作者
Abramson, Jakub [1 ]
Husebye, Eystein S. [2 ,3 ]
机构
[1] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[2] Univ Bergen, Dept Clin Sci, N-5021 Bergen, Norway
[3] Haukeland Hosp, Dept Med, N-5021 Bergen, Norway
基金
以色列科学基金会;
关键词
autoimmune regulator; autoimmune polyendocrine syndrome type-1; autoimmunity; medullary thymic epithelial cell; T-regulatory cell; autoantibodies; CANDIDIASIS-ECTODERMAL DYSTROPHY; CHRONIC MUCOCUTANEOUS CANDIDIASIS; POLYENDOCRINE SYNDROME TYPE-1; ECTOPIC GENE-EXPRESSION; AIRE DEFICIENT MICE; SYNDROME TYPE-I; RNA-POLYMERASE; T-CELLS; P-TEFB; POLYGLANDULAR SYNDROME;
D O I
10.1111/imr.12419
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The establishment of central tolerance in the thymus is critical for avoiding deleterious autoimmune diseases. Autoimmune regulator (AIRE), the causative gene in autoimmune polyendocrine syndrome type-1 (APS-1), is crucial for the establishment of self-tolerance in the thymus by promoting promiscuous expression of a wide array of tissue-restricted self-antigens. This step is critical for elimination of high-affinity self-reactive T cells from the immunological repertoire, and for the induction of a specific subset of Foxp3(+) T-regulatory (T-reg) cells. In this review, we discuss the most recent advances in our understanding of how AIRE operates on molecular and cellular levels, as well as of how its loss of function results in breakdown of self-tolerance mechanisms characterized by a broad and heterogeneous repertoire of autoimmune phenotypes.
引用
收藏
页码:127 / 140
页数:14
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