Romanescu Constantin, Schreiner Thomas Gabriel, Mukovozov Ilya
Clinical Section IV, "St. Parascheva" Infectious Disease Hospital, 700116 Iași, Romania.
Faculty of Medicine, University of Medicine and Pharmacy "Gr. T. Popa", 700115 Iasi, Romania.
J Clin Med. 2022 May 29;11(11):3061. doi: 10.3390/jcm11113061.
Alzheimer's disease (AD), a neurodegenerative disorder generally affecting older adults, is the most common form of dementia worldwide. The disease is marked by severe cognitive and psychiatric decline and has dramatic personal and social consequences. Considerable time and resources are dedicated to the pursuit of a better understanding of disease mechanisms; however, the ultimate goal of obtaining a viable treatment option remains elusive. Neurodegenerative disease as an outcome of gene-environment interaction is a notion widely accepted today; a clear understanding of how external factors are involved in disease pathogenesis is missing, however. In the case of AD, significant effort has been invested in the study of viral pathogens and their role in disease mechanisms. The current scoping review focuses on the purported role HHV-6 plays in AD pathogenesis. First, early studies demonstrating evidence of HHV-6 cantonment in either post-mortem AD brain specimens or in peripheral blood samples of living AD patients are reviewed. Next, selected examples of possible mechanisms whereby viral infection can directly or indirectly contribute to AD pathogenesis are presented, such as autophagy dysregulation, the interaction between miR155 and HHV-6, and amyloid-beta as an antimicrobial peptide. Finally, closely related topics such as HHV-6 penetration in the CNS, HHV-6 involvement in neuroinflammation, and a brief discussion on HHV-6 epigenetics are examined.
阿尔茨海默病(AD)是一种通常影响老年人的神经退行性疾病,是全球最常见的痴呆形式。该疾病以严重的认知和精神衰退为特征,并产生巨大的个人和社会后果。人们投入了大量的时间和资源来更好地理解疾病机制;然而,获得可行治疗方案的最终目标仍然难以实现。作为基因 - 环境相互作用结果的神经退行性疾病是当今广泛接受的一个概念;然而,目前尚不清楚外部因素如何参与疾病发病机制。就AD而言,人们已经在病毒病原体及其在疾病机制中的作用研究方面投入了大量精力。当前的范围综述聚焦于人类疱疹病毒6型(HHV - 6)在AD发病机制中所声称的作用。首先,回顾早期研究,这些研究证明了在死后AD脑标本或活着的AD患者外周血样本中存在HHV - 6驻留的证据。接下来,介绍病毒感染可能直接或间接导致AD发病机制的一些可能机制的选定示例,例如自噬失调、miR155与HHV - 6之间的相互作用以及淀粉样β作为一种抗菌肽。最后,研究密切相关的主题,如HHV - 6在中枢神经系统中的渗透、HHV - 6参与神经炎症以及关于HHV - 6表观遗传学的简要讨论。