Suppr超能文献

土耳其白塞病患者中Toll样受体2基因Arg753Gln多态性

Toll-like receptor 2 Arg753Gln gene polymorphism in Turkish patients with Behçet's disease.

作者信息

Bacanli A, Sallakci N, Yavuzer U, Alpsoy E, Yegin O

机构信息

Department of Dermatology and Venerology, Akdeniz University School of Medicine, Antalya, Turkey.

出版信息

Clin Exp Dermatol. 2006 Sep;31(5):699-701. doi: 10.1111/j.1365-2230.2006.02212.x.

Abstract

Having considered the impact of the function of TLR2 in the recognition of several microorganisms that are thought to have an association with Behçet's disease (BD), we aimed to determine a possible association between the TLR2 Arg753Gln polymorphism and susceptibility to BD. We genotyped 83 patients with BD, 95 ethnically matched healthy controls, 12 patients with recurrent aphthous stomatitis (RAS) and 21 patients with rheumatoid arthritis (RA) by restriction fragment length polymorphism after PCR amplification of the genomic region encompassing the polymorphic site. Comparison of the TLR2 Arg753Gln A allele and A/G genotype frequencies did not show a significant difference between patients with BD and healthy controls (1.2% vs. 0.6%, and 2.1% vs. 1.1%, respectively). None of the patients from the RAS and RA groups had the A allele or A/G genotype. Our results indicate that the TLR2 Arg753Gln polymorphism does not play a role in the aetiopathogenesis of BD.

摘要

在考虑了Toll样受体2(TLR2)功能在识别几种被认为与白塞病(BD)有关联的微生物中的作用后,我们旨在确定TLR2基因第753位密码子精氨酸(Arg)突变为谷氨酰胺(Gln)的多态性与BD易感性之间的可能关联。我们通过聚合酶链反应(PCR)扩增包含该多态性位点的基因组区域后,采用限制性片段长度多态性方法对83例BD患者、95例种族匹配的健康对照、12例复发性阿弗他口炎(RAS)患者和21例类风湿关节炎(RA)患者进行基因分型。比较TLR2基因第753位密码子Arg/Gln的A等位基因频率和A/G基因型频率,发现BD患者与健康对照之间无显著差异(分别为1.2%对0.6%,以及2.1%对1.1%)。RAS组和RA组患者均无A等位基因或A/G基因型。我们的结果表明,TLR2基因第753位密码子Arg/Gln多态性在BD的发病机制中不起作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验