Aire and T cell development

被引:93
作者
Anderson, Mark S. [1 ,2 ]
Su, Maureen A. [3 ,4 ]
机构
[1] Univ Calif San Francisco, Ctr Diabet, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[3] Univ N Carolina, Inflammatory Dis Inst, Chapel Hill, NC USA
[4] Univ N Carolina, Dept Pediat, Chapel Hill, NC USA
基金
美国国家卫生研究院;
关键词
THYMIC EPITHELIAL-CELLS; CANDIDIASIS-ECTODERMAL DYSTROPHY; PROMISCUOUS GENE-EXPRESSION; ORGAN-SPECIFIC AUTOIMMUNITY; PHD FINGER; LYMPHOTOXIN PATHWAY; CENTRAL TOLERANCE; IMMUNOLOGICAL-TOLERANCE; NEGATIVE SELECTION; SELF-TOLERANCE;
D O I
10.1016/j.coi.2010.11.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In the thymus, developing T cells that react against self-antigens with high affinity are deleted in the process of negative selection. An essential component of this process is the display of self-antigens, including those whose expression are usually restricted to specific tissues, to developing T cells within the thymus. The Autoimmune Regulator (Aire) gene plays a crucial role in the expression of tissue specific self-antigens within the thymus, and disruption of Aire function results in spontaneous autoimmunity in both humans and mice. Recent advances have been made in our understanding of how Aire influences the expression of thousands of tissue-specific antigens in the thymus. Additional roles of Aire, including roles in chemokine and cytokine expression, have also been revealed. Factors important in the differentiation of Aire-expressing medullary thymic epithelial cells have been defined. Finally, the identity of antigen presenting cells in negative selection, including the role of medullary thymic epithelial cells in displaying tissue specific antigens to T cells, has also been clarified.
引用
收藏
页码:198 / 206
页数:9
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