The relationship between HIV-1 neuroinflammation, neurocognitive impairment and encephalitis pathology: A systematic review of studies investigating post-mortem brain tissue.

IF 9 2区 医学 Q1 VIROLOGY Reviews in Medical Virology Pub Date : 2024-01-01 DOI:10.1002/rmv.2519
Monray Edward Williams, Petrus J W Naudé
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Abstract

The activities of HIV-1 in the central nervous system (CNS) are responsible for a dysregulated neuroinflammatory response and the subsequent development of HIV-associated neurocognitive disorders (HAND). The use of post-mortem human brain tissue is pivotal for studying the neuroimmune mechanisms of CNS HIV infection. To date, numerous studies have investigated HIV-1-induced neuroinflammation in post-mortem brain tissue. However, from the commonly investigated studies in this line of research, it is not clear which neuroinflammatory markers are consistently associated with HIV neurocognitive impairment (NCI) and neuropathology (i.e., HIV-encephalitis, HIVE). Therefore, we conducted a systematic review of the association between neuroinflammation and NCI/HIVE from studies investigating post-mortem brain tissue. Our aim was to synthesise the published data to date to provide commentary on the most noteworthy markers that are associated with NCI/HIVE. PubMed, Scopus, and Web of Science databases were searched using a search protocol designed specifically for this study. Sixty-one studies were included that investigated the levels of inflammatory markers based on their gene and protein expression in association with NCI/HIVE. The findings revealed that the (1) transcript expressions of IL-1β and TNF-α were consistently associated with NCI/HIVE, whereas CCL2 and IL-6 were commonly not associated with NCI/HIVE, (2) protein expressions of CD14, CD16, CD68, Iba-1, IL-1β and TNF-α were consistently associated with NCI/HIVE, while CD45, GFAP, HLA-DR, IL-1 and IL-6 were commonly not associated with NCI/HIVE, and (3) gene and protein expressions of CNS IL-1β and TNF-α were consistently associated with NCI/HIVE, while IL-6 was consistently not associated with NCI/HIVE. These markers highlight the commonly investigated markers in this line of research and elucidates the neuroinflammatory mechanisms in the HIV-1 brain that are involved in the pathophysiology of NCI/HIVE. These markers and related pathways should be investigated for the development of improved diagnostics, prognostics, and therapeutics of HAND.

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HIV-1 神经炎症、神经认知障碍和脑炎病理之间的关系:对死后脑组织调查研究的系统回顾。
HIV-1 在中枢神经系统(CNS)中的活动是导致神经炎症反应失调以及随后出现 HIV 相关神经认知障碍(HAND)的原因。使用死后人类脑组织是研究中枢神经系统 HIV 感染的神经免疫机制的关键。迄今为止,已有许多研究调查了死后脑组织中 HIV-1 诱导的神经炎症。然而,从这一研究方向的常见调查研究来看,尚不清楚哪些神经炎症标志物与 HIV 神经认知障碍(NCI)和神经病理学(即 HIV-脑炎,HIVE)始终相关。因此,我们对调查死后脑组织的研究中神经炎症与 NCI/HIVE 之间的关联进行了系统性回顾。我们的目的是综合迄今为止已发表的数据,对与 NCI/HIVE 相关的最值得注意的标记物进行评述。我们使用专门为本研究设计的搜索协议对 PubMed、Scopus 和 Web of Science 数据库进行了搜索。共收录了 61 项研究,这些研究根据炎症标志物的基因和蛋白表达水平调查了其与 NCI/HIVE 的相关性。研究结果表明:(1) IL-1β 和 TNF-α 的转录本表达与 NCI/HIVE 始终相关,而 CCL2 和 IL-6 通常与 NCI/HIVE 无关;(2) CD14、CD16、CD68、Iba-1、IL-1β 和 TNF-α 的蛋白表达与 NCI/HIVE 始终相关,而 CD45、GFAP、HL-6 和 IL-1β 则与 NCI/HIVE 无关、(3) 中枢神经系统 IL-1β 和 TNF-α 的基因和蛋白表达与 NCI/HIVE 始终相关,而 IL-6 与 NCI/HIVE 始终无关。这些标记物突出了这一研究方向中常用的调查标记物,并阐明了参与 NCI/HIVE 病理生理学的 HIV-1 大脑神经炎症机制。应研究这些标记物和相关途径,以开发更好的 HAND 诊断、预后和治疗方法。
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来源期刊
Reviews in Medical Virology
Reviews in Medical Virology 医学-病毒学
CiteScore
21.40
自引率
0.90%
发文量
88
期刊介绍: Reviews in Medical Virology aims to provide articles reviewing conceptual or technological advances in diverse areas of virology. The journal covers topics such as molecular biology, cell biology, replication, pathogenesis, immunology, immunization, epidemiology, diagnosis, treatment of viruses of medical importance, and COVID-19 research. The journal has an Impact Factor of 6.989 for the year 2020. The readership of the journal includes clinicians, virologists, medical microbiologists, molecular biologists, infectious disease specialists, and immunologists. Reviews in Medical Virology is indexed and abstracted in databases such as CABI, Abstracts in Anthropology, ProQuest, Embase, MEDLINE/PubMed, ProQuest Central K-494, SCOPUS, and Web of Science et,al.
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