| Literature DB >> 32024769 |
Tiphaine C Martin1, Mirna Šimurina2, Marta Ząbczyńska3, Marina Martinic Kavur4, Magdalena Rydlewska3, Marija Pezer4, Kamila Kozłowska3, Andrea Burri5, Marija Vilaj4, Renata Turek-Jabrocka6, Milena Krnjajić-Tadijanović7, Małgorzata Trofimiuk-Müldner6, Ivo Ugrina8, Anna Lityńska3, Alicja Hubalewska-Dydejczyk6, Irena Trbojevic-Akmacic4, Ee Mun Lim9, John P Walsh9, Ewa Pocheć3, Tim D Spector10, Scott G Wilson11, Gordan Lauc12.
Abstract
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.Entities:
Keywords: IgG; Immunology; antibodies; antibody-dependent cell-mediated cytotoxicity (ADCC); autoimmune thyroid disease; fucosylation; glycoproteins; glycosylation; patient cohorts; thyroid peroxidase antibodies (TPOAb)
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Year: 2020 PMID: 32024769 PMCID: PMC7196582 DOI: 10.1074/mcp.RA119.001860
Source DB: PubMed Journal: Mol Cell Proteomics ISSN: 1535-9476 Impact factor: 5.911