| Literature DB >> 35459628 |
Hanna J Lee1, Mihaela Stefan-Lifshitz2, Cheuk Wun Li3, Yaron Tomer4.
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 (Tg1, TSHR, HLA-DR3, and CD40) and their translational therapeutic potential.Entities:
Keywords: CD40; HLA; TSHR; autoimmune thyroid disease; genes; thyroglobulin
Year: 2022 PMID: 35459628 PMCID: PMC9550878 DOI: 10.1016/j.beem.2022.101661
Source DB: PubMed Journal: Best Pract Res Clin Endocrinol Metab ISSN: 1521-690X Impact factor: 5.667