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来自匈牙利的多发性硬化症患者及配对对照所排出的JC病毒。

JC virus excreted by multiple sclerosis patients and paired controls from Hungary.

作者信息

Stoner G L, Agostini H T, Ryschkewitsch C F, Komoly S

机构信息

Neurotoxicology Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Mult Scler. 1998 Apr;4(2):45-8. doi: 10.1177/135245859800400201.

Abstract

JC virus (JCV), a human polyomavirus, is the agent of the demyelinating disease progressive multifocal leukoencephalopathy (PML). JCV exists in four main genotypes in the USA. Type 1, including subtypes Type 1A and Type 1B, makes up about 64% of strains in the USA and is thought to be of European origin. Type 2 is found in Asia, and Type 3 in Africa. A fourth type is found only in the USA. In general, these genotypes differ in 1-2.5% of their DNA sequence. Thirty MS patients and 30 paired controls from Budapest were studied. The clinical course of MS was mainly secondary progressive, and patients were stable at the time of testing. Most of the controls were relatives of the probands: a spouse, parent, or child. Overall, 25 of 60 (42%) of the urines tested positive for JCV by PCR. These included 13 of 30 MS patients, and 12 of 30 controls. Genotyping in the VPI gene showed all 25 JCV strains to be Type 1. Among the MS patients, seven were Type 1A and six were Type 1B. Among the controls, nine were Type 1A and three were Type 1B. In five pairs of MS patients and controls, both were positive for JCV by PCR. Two of these were husband/wife pairs of which one pair was matched for subtype (both Type 1A), and the other was not. Two of them were mother/daughter pairs, and both were matched for subtype (both Type 1B). These findings demonstrate that JCV Type 1 predominates among Hungarians, and suggest that parent/child pairs can be used to trace JCV transmission within the MS family.

摘要

JC病毒(JCV)是一种人类多瘤病毒,是脱髓鞘疾病进行性多灶性白质脑病(PML)的病原体。在美国,JCV存在四种主要基因型。1型,包括1A亚型和1B亚型,占美国毒株的约64%,被认为起源于欧洲。2型在亚洲发现,3型在非洲发现。第四种类型仅在美国发现。一般来说,这些基因型的DNA序列有1 - 2.5%的差异。对来自布达佩斯的30例多发性硬化症(MS)患者和30例配对对照进行了研究。MS的临床病程主要为继发进展型,患者在检测时病情稳定。大多数对照是先证者的亲属:配偶、父母或子女。总体而言,60份尿液样本中有25份(42%)通过PCR检测JCV呈阳性。其中包括30例MS患者中的13例,以及30例对照中的12例。VPI基因的基因分型显示,所有25株JCV毒株均为1型。在MS患者中,7例为1A亚型,6例为1B亚型。在对照中,9例为1A亚型,3例为1B亚型。在5对MS患者和对照中,两者通过PCR检测JCV均为阳性。其中2对是夫妻,一对亚型匹配(均为1A亚型),另一对不匹配。另外2对是母女,两者亚型匹配(均为1B亚型)。这些发现表明,1型JCV在匈牙利人中占主导地位,并表明亲子对可用于追踪MS家族内的JCV传播。

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