Department of Twin Research and Genetic Epidemiology, King's College, London, United Kingdom; School of Biomedical Sciences, University of Western Australia, Crawley, Western Australia, Australia.
Faculty of Pharmacy and Biochemistry, University of Zagreb, Zagreb, Croatia.
Mol Cell Proteomics. 2020 May;19(5):774-792. doi: 10.1074/mcp.RA119.001860. Epub 2020 Feb 5.
Autoimmune thyroid diseases (AITD) are the most common group of autoimmune diseases, associated with lymphocyte infiltration and the production of thyroid autoantibodies, like thyroid peroxidase antibodies (TPOAb), in the thyroid gland. Immunoglobulins and cell-surface receptors are glycoproteins with distinctive glycosylation patterns that play a structural role in maintaining and modulating their functions. We investigated associations of total circulating IgG and peripheral blood mononuclear cells glycosylation with AITD and the influence of genetic background in a case-control study with several independent cohorts and over 3,000 individuals in total. The study revealed an inverse association of IgG core fucosylation with TPOAb and AITD, as well as decreased peripheral blood mononuclear cells antennary α1,2 fucosylation in AITD, but no shared genetic variance between AITD and glycosylation. These data suggest that the decreased level of IgG core fucosylation is a risk factor for AITD that promotes antibody-dependent cell-mediated cytotoxicity previously associated with TPOAb levels.
自身免疫性甲状腺疾病 (AITD) 是最常见的一组自身免疫性疾病,与甲状腺中的淋巴细胞浸润和甲状腺自身抗体(如甲状腺过氧化物酶抗体,TPOAb)的产生有关。免疫球蛋白和细胞表面受体是糖蛋白,具有独特的糖基化模式,在维持和调节其功能方面发挥结构作用。我们在一项病例对照研究中,对多个独立队列的 3000 多人进行了研究,调查了总循环 IgG 和外周血单核细胞糖基化与 AITD 的关联,以及遗传背景的影响。研究表明,IgG 核心岩藻糖基化与 TPOAb 和 AITD 呈负相关,AITD 患者外周血单核细胞触角α1,2 岩藻糖基化减少,但 AITD 和糖基化之间没有共同的遗传变异。这些数据表明,IgG 核心岩藻糖基化水平降低是 AITD 的一个风险因素,它促进了先前与 TPOAb 水平相关的抗体依赖性细胞介导的细胞毒性。