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人类内源性逆转录病毒-K18包膜蛋白作为多发性硬化症的一个风险因素。

Human endogenous retrovirus-K18 Env as a risk factor in multiple sclerosis.

作者信息

Tai A K, O'Reilly E J, Alroy K A, Simon K C, Munger K L, Huber B T, Ascherio A

机构信息

Department of Pathology, Tufts University School of Medicine, Boston, Massachusetts, USA.

出版信息

Mult Scler. 2008 Nov;14(9):1175-80. doi: 10.1177/1352458508094641. Epub 2008 Aug 13.

Abstract

BackgroundThe human endogenous retrovirus (HERV)-K18 Env is an Epstein-Barr virus (EBV)-associated superantigen. Given the evidence for a role of EBV in the etiology of multiple sclerosis (MS), HERV-K18 Env is a plausible candidate for association with MS.ObjectiveTo assess whether variation in HERV-K18 Env is a risk factor for MS.MethodsWe developed a single nucleotide polymorphism-based genotyping method to determine the distribution of the three alleles of HERV-K18 env. We then conducted a nested case-control study including 207 MS cases and 403 matched controls. Analyses were replicated in an independent series of 909 MS cases and 339 controls.ResultsOverall, there was a significant association between HERV-K18 env genotype and MS risk (chi2 P = 0.03). As compared with K18.2/K18.2 individuals, risk of MS was three fold higher among K18.3/K18.3 individuals (P = 0.03). An increase in MS risk among carriers of the K18.3 allele was also observed in the replication study, but did not reach statistical significance. In pooled analyses, K18.3/K18.3 individuals had a significantly increased risk of MS (relative risks [RR] comparing K18.3/K18.3 vs K18.2/K18.2 = 2.7; 95% confidence interval: 1.1-6.4).ConclusionVariation in EBV-associated superantigen HERV-K18 Env could influence the genetic susceptibility to MS.

摘要

背景

人类内源性逆转录病毒(HERV)-K18 Env是一种与爱泼斯坦-巴尔病毒(EBV)相关的超抗原。鉴于EBV在多发性硬化症(MS)病因学中的作用证据,HERV-K18 Env是与MS相关的一个合理候选因素。

目的

评估HERV-K18 Env的变异是否为MS的危险因素。

方法

我们开发了一种基于单核苷酸多态性的基因分型方法来确定HERV-K18 env三个等位基因的分布。然后我们进行了一项巢式病例对照研究,包括207例MS病例和403例匹配对照。在一个独立的909例MS病例和339例对照系列中重复分析。

结果

总体而言,HERV-K18 env基因型与MS风险之间存在显著关联(卡方检验P = 0.03)。与K18.2/K18.2个体相比,K18.3/K18.3个体患MS的风险高出三倍(P = 0.03)。在重复研究中也观察到K18.3等位基因携带者的MS风险增加,但未达到统计学显著性。在汇总分析中,K18.3/K18.3个体患MS的风险显著增加(比较K18.3/K18.3与K18.2/K18.2的相对风险[RR] = 2.7;95%置信区间:1.1 - 6.4)。

结论

与EBV相关的超抗原HERV-K18 Env的变异可能影响MS的遗传易感性。

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