疱疹病毒在阿尔茨海默病的发病机制中起作用吗?

Q3 Pharmacology, Toxicology and Pharmaceutics
Mary Alice Allnutt, Steven Jacobson
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引用次数: 4

摘要

最近的研究重新引起了人们对感染在阿尔茨海默病(AD)发病机制中起作用的假设的兴趣。特别是,单纯疱疹病毒-1 (HSV-1)和人类疱疹病毒-6 (HHV-6)等疱疹病毒与AD有广泛的关联史。病毒感染与多种神经系统疾病之间的相互作用长期以来一直是一个令人感兴趣的领域,但证明因果关系一直难以捉摸。最近的两项研究,Readhead等人(2018)和Eimer等人(2018)再次引发了关于病原体(疱疹病毒)在AD中的作用的争论。在这篇综述中,我们将简要讨论支持疱疹病毒在阿尔茨海默病发病机制中的作用的文献,并试图将阿尔茨海默病研究中的两个主要观察结果联系起来;Aβ与病原体聚集的能力,以及与非AD对照相比,AD脑物质中疱疹病毒的检测。虽然将阿尔茨海默病和人类疱疹病毒联系起来的数据表明,这些病原体可能有助于疾病进展,但需要进一步的工作来确定这些观察结果(如果有的话)对疾病病因的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Do herpesviruses play a role in Alzheimer’s disease pathogenesis?

Recent studies have brought renewed interest to the hypothesis that infection plays a role in the pathogenesis of Alzheimer’s disease (AD). In particular, herpesviruses such as herpes simplex virus-1 (HSV-1) and human herpesvirus-6 (HHV-6) have had an extensive history of association with AD. The interplay between viral infection and a variety of neurological diseases has long been an area of interest but proving causality has been elusive. Two recent studies, Readhead et al. (2018) and Eimer et al. (2018) have again renewed the debate concerning the role of pathogens (herpesviruses) in AD. In this review, we will briefly discuss the literature in support of a herpesvirus role in AD pathogenesis and try to bridge two main observations in AD research; the ability of Aβ to aggregate with pathogens, and the detection of herpesviruses in AD brain material compared to non-AD controls. While the data linking AD and human herpesviruses suggest that these pathogens may contribute to disease progression, further work is needed to determine the significance of these observations, if any, to the etiology of the disease.

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来源期刊
Drug Discovery Today: Disease Models
Drug Discovery Today: Disease Models Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
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期刊介绍: Drug Discovery Today: Disease Models discusses the non-human experimental models through which inference is drawn regarding the molecular aetiology and pathogenesis of human disease. It provides critical analysis and evaluation of which models can genuinely inform the research community about the direct process of human disease, those which may have value in basic toxicology, and those which are simply designed for effective expression and raw characterisation.
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