The CD40, CTLA-4, thyroglobulin, TSH receptor, and PTPN22 gene quintet and its contribution to thyroid autoimmunity:: Back to the future

被引:142
作者
Jacobson, Eric M.
Tomer, Yaron
机构
[1] Univ Cincinnati, Vontz Ctr Mol Studies, Div Endocrinol, Cincinnati, OH 45267 USA
[2] Univ Cincinnati, Cincinnati VA Med Ctr, Coll Med, Cincinnati, OH 45267 USA
关键词
immunoregulation; organ specific autoimmunity; genetics; autoimmune thyroiditis;
D O I
10.1016/j.jaut.2007.02.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Autoimmune thyroid diseases (AITD) are common autoimmune diseases, affecting up to 5% of the general population. Thyroid-directed autommunity is manifested in two classical autoimmune conditions, Hashimoto's thyroiditis, resulting in hypothyroidism and Graves' disease resulting in hyperthyroidism. Autoimmune thyroid diseases arise due to an interplay between environmental and genetic factors. In the past decade significant progress has been made in our understanding of the genetic contribution to the etiology of AITD. Indeed, several AITD susceptibility genes have been identified. Some of these susceptibility genes are specific to either Graves' disease or Hashimoto's thyroiditis, while others confer susceptibility to both conditions. Both immunoregulatory genes and thyroid specific genes contribute to the pathogenesis of AITD. The time is now ripe to examine the mechanistic basis for the contribution of genetic factors to the etiology of AITD. In this review, we will focus on the contribution of non-MHC II genes. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:85 / 98
页数:14
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