Possible link of genetic variants to autoimmunity in GAD-antibody-associated neurological disorders

Thaler, Franziska S.; Bangol, Barbara; Biljecki, Michelle; Havla, Joachim; Schumacher, Adrian-Minh und Kuempfel, Tania (2020): Possible link of genetic variants to autoimmunity in GAD-antibody-associated neurological disorders. In: Journal of the Neurological Sciences, Bd. 413, 116860

Abstract

Objective: In patients with GAD-antibody (ab) associated neurological disorders coexistence of other autoimmune disorders is observed. Methods: In this exploratory study we analysed variations in 33 candidate genes involved in autoimmunity or representing immunological check-points using next-generation sequencing. We performed haplotype-analysis of HLA-DRB1 and HLA-DQB1. Additionally, we analysed levels of sFasL, IL10, and IL18 in serum of patients and healthy controls. Results: 19 patients (3 males, 16 females;mean age at onset: 46.4 years) with positive GAD-ab and the following neurological phenotypes were included: n = 8 cerebellar ataxia, n = 6 limbic encephalitis, n = 4 stiff person syndrome, n = 1 demyelinating CNS disease with recurrent optic neuritis. 15 patients exhibited at least one other autoimmune disorder and/or showed other auto-ab. We identified several variations in genes linked to autoimmunity or representing check-point proteins. Most frequently (14/19 patients, allele frequency: 42.1%), we observed an amino acid exchange in the cytotoxic T-lymphocyte-associated protein 4 (CTLA4) gene. Two of the observed variants are known to cause alterations of protein function (Y446C in caspase-10, K750N in proteintyrosin-phosphatase, non-receptor type 22). These latter variants were detected in two related patients (mother and daughter) who both present with GAD-ab-associated neurological disorders but with different clinical phenotypes. The rare haplotype DRB1*15:01:01 similar to DQA1*01:02:01 similar to DQB1*05:02:01 previously described in patients with GAD-ab-associated neurological disorders was not observed in any of our patients. No elevated serum levels of sFasL, IL18 or IL10 were observed in patients indicating no typical phenotype of autoimmune lymphoproliferate syndrome. Conclusions: These findings suggest genetic risk factors in patients with GAD-ab-associated neurological disorders.

• Dokumententyp: Zeitschriftenartikel
• Fakultät: Medizin
• Themengebiete: 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit
• ISSN: 0022-510X
• Sprache: Englisch