Vaidya Bijay, Pearce Simon
Department of Diabetes, Endocrinology and Vascular Medicine, Peninsula Medical School, Royal Devon and Exeter Hospital, Exeter EX2 5DW, UK.
Eur J Endocrinol. 2004 May;150(5):619-26. doi: 10.1530/eje.0.1500619.
It is thought that the majority of autoimmune endocrinopathies, including Graves' disease, autoimmune hypothyroidism, type 1 diabetes mellitus and autoimmune Addison's disease (sporadic and as well as autoimmune polyendocrinopathy syndrome type 2) are inherited as complex genetic traits. Multiple genetic and environmental factors interact with each other to confer susceptibility to these disorders. In recent years there have been considerable efforts towards defining susceptibility genes for complex traits. These investigations have shown, with increasing evidence, that the cytotoxic T lymphocyte antigen-4 (CTLA-4) gene is an important susceptibility locus for autoimmune endocrinopathies and other autoimmune disorders. Here we review the genetic and functional analyses of the CTLA-4 locus in autoimmune endocrinopathies, and discuss the recent efforts in fine-mapping this locus.
人们认为,大多数自身免疫性内分泌疾病,包括格雷夫斯病、自身免疫性甲状腺功能减退症、1型糖尿病和自身免疫性艾迪生病(散发性以及2型自身免疫性多内分泌腺病综合征),都是作为复杂的遗传性状遗传的。多种遗传和环境因素相互作用,使人易患这些疾病。近年来,人们为确定复杂性状的易感基因付出了巨大努力。这些研究越来越多地表明,细胞毒性T淋巴细胞抗原4(CTLA-4)基因是自身免疫性内分泌疾病和其他自身免疫性疾病的一个重要易感位点。在此,我们综述了自身免疫性内分泌疾病中CTLA-4位点的遗传和功能分析,并讨论了该位点精细定位的最新研究进展。