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痴呆、感染和疫苗:30 年的争议。

Dementia, infections and vaccines: 30 years of controversy.

机构信息

EA3920, University of Franche-Comté, 25000, Besancon, France.

Department of Cardiology, University Hospital Besancon, 3-8 Boulevard Fleming, 25000, Besancon, France.

出版信息

Aging Clin Exp Res. 2023 Jun;35(6):1145-1160. doi: 10.1007/s40520-023-02409-8. Epub 2023 May 9.

DOI:10.1007/s40520-023-02409-8
PMID:37160649
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10169152/
Abstract

This paper reports the proceedings of a virtual meeting convened by the European Interdisciplinary Council on Ageing (EICA), to discuss the involvement of infectious disorders in the pathogenesis of dementia and neurological disorders leading to dementia. We recap how our view of the infectious etiology of dementia has changed over the last 30 years in light of emerging evidence, and we present evidence in support of the implication of infection in dementia, notably Alzheimer's disease (AD). The bacteria and viruses thought to be responsible for neuroinflammation and neurological damage are reviewed. We then review the genetic basis for neuroinflammation and dementia, highlighting the genes that are currently the focus of investigation as potential targets for therapy. Next, we describe the antimicrobial hypothesis of dementia, notably the intriguing possibility that amyloid beta may itself possess antimicrobial properties. We further describe the clinical relevance of the gut-brain axis in dementia, the mechanisms by which infection can move from the intestine to the brain, and recent findings regarding dysbiosis patterns in patients with AD. We review the involvement of specific pathogens in neurological disorders, i.e. SARS-CoV-2, human immunodeficiency virus (HIV), herpes simplex virus type 1 (HSV1), and influenza. Finally, we look at the role of vaccination to prevent dementia. In conclusion, there is a large body of evidence supporting the involvement of various infectious pathogens in the pathogenesis of dementia, but large-scale studies with long-term follow-up are needed to elucidate the role that infection may play, especially before subclinical or clinical disease is present.

摘要

本文报告了欧洲跨学科老龄化研究理事会(EICA)召开的一次虚拟会议的会议记录,该会议旨在讨论传染病在痴呆症和导致痴呆的神经紊乱发病机制中的作用。我们回顾了过去 30 年来,鉴于新出现的证据,我们对痴呆症传染病病因的看法发生了怎样的变化,并提供了支持感染在痴呆症,特别是阿尔茨海默病(AD)中起作用的证据。文中回顾了被认为与神经炎症和神经损伤有关的细菌和病毒。然后,我们回顾了神经炎症和痴呆症的遗传基础,重点介绍了目前作为治疗潜在靶点而受到关注的基因。接下来,我们描述了痴呆症的抗菌假说,特别是令人着迷的可能性,即淀粉样蛋白β本身可能具有抗菌特性。我们进一步描述了痴呆症中肠脑轴的临床相关性、感染从肠道转移到大脑的机制以及 AD 患者中菌群失调模式的最新发现。我们回顾了特定病原体在神经紊乱中的作用,即 SARS-CoV-2、人类免疫缺陷病毒(HIV)、单纯疱疹病毒 1 型(HSV1)和流感。最后,我们研究了疫苗在预防痴呆症中的作用。总之,有大量证据支持各种传染病原在痴呆症发病机制中的作用,但需要进行大规模的长期随访研究,以阐明感染可能发挥的作用,尤其是在出现亚临床或临床疾病之前。

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Exercise-Induced ADAR2 Protects against Nonalcoholic Fatty Liver Disease through miR-34a.运动诱导的 ADAR2 通过 miR-34a 来预防非酒精性脂肪性肝病。
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Does the imbalance in the apolipoprotein E isoforms underlie the pathophysiological process of sporadic Alzheimer's disease?载脂蛋白E亚型的失衡是否是散发性阿尔茨海默病病理生理过程的基础?
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