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自身免疫性甲状腺疾病的遗传学和表观遗传学:转化意义。

Genetics and epigenetics of autoimmune thyroid diseases: Translational implications.

机构信息

Department of Medicine, The Fleischer Institute for Diabetes and Metabolism, Albert Einstein College of Medicine, New York, NY, USA.

出版信息

Best Pract Res Clin Endocrinol Metab. 2023 Mar;37(2):101661. doi: 10.1016/j.beem.2022.101661. Epub 2022 Apr 11.

Abstract

Hashimoto's thyroiditis (HT) and Graves' disease (GD) are prevalent autoimmune disorders, representing opposite ends of the clinical spectrum of autoimmune thyroid diseases (AITD). The pathogenesis involves a complex interplay between environment and genes. Specific susceptibility genes have been discovered that predispose to AITD, including thyroid-specific and immune-regulatory genes. Growing evidence has revealed that genetic and epigenetic variants can alter autoantigen presentation during the development of immune tolerance, can enhance self-peptide binding to MHC (major histocompatibility complex), and can amplify stimulation of T- and B-cells. These gene-driven mechanistic discoveries lay the groundwork for novel treatment targets. This review summarizes recent advances in our understanding of key AITD susceptibility genes (Tg, TSHR, HLA-DR3, and CD40) and their translational therapeutic potential.

摘要

桥本甲状腺炎(HT)和格雷夫斯病(GD)是常见的自身免疫性疾病,代表了自身免疫性甲状腺疾病(AITD)临床谱的两个极端。其发病机制涉及环境和基因之间的复杂相互作用。已经发现了特定的易感基因,这些基因易导致 AITD,包括甲状腺特异性和免疫调节基因。越来越多的证据表明,遗传和表观遗传变异可以改变免疫耐受过程中自身抗原的呈递方式,可以增强自身肽与 MHC(主要组织相容性复合体)的结合,并可以放大 T 细胞和 B 细胞的刺激作用。这些由基因驱动的机制发现为新型治疗靶点奠定了基础。本综述总结了我们对关键 AITD 易感基因(Tg、TSHR、HLA-DR3 和 CD40)及其潜在转化治疗的最新认识。

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