Hogestyn Jessica M, Mock David J, Mayer-Proschel Margot
Department of Neuroscience, University of Rochester, Rochester, NY, USA.
Department of Biomedical Genetics, University of Rochester, Rochester, NY, USA.
Neural Regen Res. 2018 Feb;13(2):211-221. doi: 10.4103/1673-5374.226380.
Human herpesviruses (HVs) have developed ingenious mechanisms that enable them to traverse the defenses of the central nervous system (CNS). The ability of HVs to enter a state of latency, a defining characteristic of this viral family, allows them to persist in the human host indefinitely. As such, HVs represent the most frequently detected pathogens in the brain. Under constant immune pressure, these infections are largely asymptomatic in healthy hosts. However, many neurotropic HVs have been directly connected with CNS pathology in the context of other stressors and genetic risk factors. In this review, we discuss the potential mechanisms by which neurotropic HVs contribute to neurodegenerative disease (NDD) pathology by highlighting two prominent members of the HV family, herpes simplex virus 1 (HSV-1) and human herpesvirus 6 (HHV-6). We (i) introduce the infectious pathways and replicative cycles of HSV-1 and HHV-6 and then (ii) review the clinical evidence supporting associations between these viruses and the NDDs Alzheimer's disease (AD) and multiple sclerosis (MS), respectively. We then (iii) highlight and discuss potential mechanisms by which these viruses exert negative effects on neurons and glia. Finally, we (iv) discuss how these viruses could interact with other disease-modifying factors to contribute to the initiation and/or progression of NDDs.
人类疱疹病毒(HVs)已经进化出巧妙的机制,使其能够突破中枢神经系统(CNS)的防御。HVs进入潜伏状态的能力是这个病毒家族的一个决定性特征,这使得它们能够在人类宿主中无限期持续存在。因此,HVs是大脑中最常检测到的病原体。在持续的免疫压力下,这些感染在健康宿主中大多无症状。然而,在其他应激源和遗传风险因素的背景下,许多嗜神经HVs已与中枢神经系统病理学直接相关。在这篇综述中,我们通过重点介绍疱疹病毒家族的两个主要成员,即单纯疱疹病毒1型(HSV-1)和人类疱疹病毒6型(HHV-6),来讨论嗜神经HVs导致神经退行性疾病(NDD)病理的潜在机制。我们(i)介绍HSV-1和HHV-6的感染途径和复制周期,然后(ii)分别回顾支持这些病毒与NDDs阿尔茨海默病(AD)和多发性硬化症(MS)之间关联的临床证据。接着,我们(iii)强调并讨论这些病毒对神经元和神经胶质细胞产生负面影响的潜在机制。最后,我们(iv)讨论这些病毒如何与其他疾病修饰因子相互作用,从而导致NDDs的发生和/或进展。