A Guillain-Barré syndrome-associated SIGLEC10 rare variant impairs its recognition of gangliosides. Issue 116 (January 2021)

• Record Type: Journal Article
• Authors: Alborzian Deh Sheikh, Amin; Gomaa, Soha; Li, Xuexin; Routledge, Matthew; Saigoh, Kazumasa; Numoto, Nobutaka; Angata, Takashi; Hitomi, Yuki; Takematsu, Hiromu; Tsuiji, Makoto; Ito, Nobutoshi; Kusunoki, Susumu; Tsubata, Takeshi
• Is Part Of: Journal of autoimmunity. Issue 116(2020)
• Publication Date: 2021-01
• Subjects: Guillain-barré syndrome -- Gangliosides -- Siglec-10 -- Rare variant; Autoimmunity -- Periodicals; Autoimmune diseases -- Periodicals; Autoantibodies -- Periodicals; Autoimmune Diseases -- Periodicals; Auto-immunité -- Périodiques; Maladies auto-immunes -- Périodiques; Electronic journals; 616.978005
• DOI: 10.1016/j.jaut.2020.102571
• Languages: English
• ISSNs: 0896-8411

Abstract

Abstracts: Guillain-Barré syndrome (GBS), including its variant Miller Fisher syndrome (MFS), is an acute peripheral neuropathy that involves autoimmune mechanisms leading to the production of autoantibodies to gangliosides; sialic acid-containing glycosphingolipids. Although association with various genetic polymorphisms in the major histocompatibility complex (MHC) is shown in other autoimmune diseases, GBS is an exception, showing no such link. No significant association was found by genome wide association studies, suggesting that GBS is not associated with common variants. To address the involvement of rare variants in GBS, we analyzed Siglec-10, a sialic acid-recognizing inhibitory receptor expressed on B cells. Here we demonstrate that two rare variants encoding R47Q and A108V substitutions in the ligand-binding domain are significantly accumulated in patients with GBS. Because of strong linkage disequilibrium, there was no patient carrying only one of them. Recombinant Siglec-10 protein containing R47Q but not A108V shows impaired binding to gangliosides. Homology modeling revealed that the R47Q substitution causes marked alteration in the ligand-binding site. Thus, GBS is associated with a rare variant of the SIGLEC10 gene that impairs ligand binding of Siglec-10. Because Siglec-10 regulates antibody production to sialylated antigens, our finding suggests that Siglec-10 regulates development of GBS by suppressing antibody production to gangliosides, with defects in its function predisposing to disease. Highlights: A rare variant of the SIGLEC10 gene is a risk factor for Guillain-Barré syndrome. This variant impairs recognition of gangliosides, the self-antigen, by Siglec-10. This variant alters the structure of the ligand-binding domain of Siglec-10. Siglec-10 may specifically inhibit autoantibody production in Guillain-Barré syndrome.