Suppr超能文献

多发性硬化症和视神经炎中的肿瘤坏死因子α - 308等位基因

Tumor necrosis factor alpha-308 alleles in multiple sclerosis and optic neuritis.

作者信息

He B, Navikas V, Lundahl J, Söderström M, Hillert J

机构信息

Department of Neurology, Karolinska Institute, Huddinge Hospital, Sweden.

出版信息

J Neuroimmunol. 1995 Dec 31;63(2):143-7. doi: 10.1016/0165-5728(95)00138-7.

Abstract

Tumor necrosis factor-alpha (TNF-alpha), a proinflammatory cytokine, is believed to play an important role in multiple sclerosis (MS) pathogenesis. A bi-allelic polymorphism in the TNF-alpha promoter region (TNF alpha-308), has been reported to influence levels of TNF-alpha production. In the present study, we investigated the TNF alpha-308 polymorphism in 93 patients with MS, 17 patients with optic neuritis (ON) and 95 healthy individuals using an allele-specific PCR technique. Allelic genotype was compared with TNF-alpha mRNA expression levels and HLA class II phenotypes. No significant difference regarding the TNF alpha-308 polymorphism was observed between MS patients and controls. Specifically, the less common allele, TNF2, which is associated with higher expression levels of TNF-alpha, was somewhat less frequent among MS patients. In fact, analysis of 19 patients homozygous for the MS associated HLA-DR-DQ haplotype HLA-Dw2 showed that this haplotype does not carry the TNF2 allele. In addition, in 47 patients, the TNF-alpha alleles did not correlate with expression levels measured as numbers of TNF-alpha expressing cells. Thus, we found no evidence for an important role of TNF alpha-308 polymorphism for genetic susceptibility to MS.

摘要

肿瘤坏死因子-α(TNF-α)是一种促炎细胞因子,被认为在多发性硬化症(MS)的发病机制中起重要作用。据报道,TNF-α启动子区域的双等位基因多态性(TNFα-308)会影响TNF-α的产生水平。在本研究中,我们使用等位基因特异性PCR技术,对93例MS患者、17例视神经炎(ON)患者和95名健康个体的TNFα-308多态性进行了研究。将等位基因基因型与TNF-α mRNA表达水平和HLA II类表型进行了比较。在MS患者和对照组之间,未观察到TNFα-308多态性的显著差异。具体而言,与较高TNF-α表达水平相关的较罕见等位基因TNF2,在MS患者中的频率略低。事实上,对19例与MS相关的HLA-DR-DQ单倍型HLA-Dw2纯合的患者进行分析发现,该单倍型不携带TNF2等位基因。此外,在47例患者中,TNF-α等位基因与以TNF-α表达细胞数量衡量的表达水平不相关。因此,我们没有发现证据表明TNFα-308多态性在MS遗传易感性中起重要作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验