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CDS1 and promoter single nucleotide polymorphisms of the CTLA-4 gene in human myasthenia gravis.

作者信息

Wang X B, Kakoulidou M, Qiu Q, Giscombe R, Huang DeRen, Pirskanen R, Lefvert A K

机构信息

Immunological Research Unit, Center for Molecular Medicine and Department of Medicine, Karolinska Institutet, Stockholm, Sweden.

出版信息

Genes Immun. 2002 Feb;3(1):46-9. doi: 10.1038/sj.gene.6363816.

DOI:10.1038/sj.gene.6363816
PMID:11857062
Abstract

The cytotoxic T lymphocyte associated protein 4 (CTLA-4) gene (Ctla-4) is a candidate gene for autoimmune disease. We here report results of two single nucleotide polymorphisms (SNPs) in the Ctla-4, a +49 A/G SNP in CDS1 and a C/T promoter SNP at position -318. There were no differences in these two SNPs between patients and healthy individuals. The frequency of allele G and genotype G/G at position +49 in CDS1 was increased in patients with thymoma when compared with patients with normal and hyperplastic thymic histopathology. Patients with the G/G genotype had signs of immune activation manifested as higher levels of serum IL-1beta and higher percentage of CD28(+) T lymphocytes. There was a strong linkage between the 86bp allele in the 3'-UTR and the A(+49) allele in CDS1. Our results suggest that the SNP at position +49 in CDS1 might be associated with the manifestations of MG.

摘要

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