Department of Pathology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY, USA.
Department of Pathology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY, USA; Department of Microbiology and Immunology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY, USA.
Brain Res. 2019 Dec 1;1724:146426. doi: 10.1016/j.brainres.2019.146426. Epub 2019 Aug 29.
Approximately 37 million people worldwide are infected with human immunodeficiency virus (HIV). One highly significant complication of HIV infection is the development of HIV-associated neurocognitive disorders (HAND) in 15-55% of people living with HIV (PLWH), that persists even in the antiretroviral therapy (ART) era. The entry of HIV into the central nervous system (CNS) occurs within 4-8 days after peripheral infection. This establishes viral reservoirs that may persist even in the presence of ART. Once in the CNS, HIV infects resident macrophages, microglia, and at low levels, astrocytes. In response to chronic infection and cell activation within the CNS, viral proteins, inflammatory mediators, and host and viral neurotoxic factors produced over extended periods of time result in neuronal injury and loss, cognitive deficits and HAND. Substance abuse is a common comorbidity in PLWH and has been shown to increase neuroinflammation and cognitive disorders. Additionally, it has been associated with poor ART adherence, and increased viral load in the cerebrospinal fluid (CSF), that may also contribute to increased neuroinflammation and neuronal injury. Studies have examined mechanisms that contribute to neuroinflammation and neuronal damage in PLWH, and how substances of abuse exacerbate these effects. This review will focus on how substances of abuse, with an emphasis on methamphetamine (meth), cocaine, and opioids, impact blood brain barrier (BBB) integrity and transmigration of HIV-infected and uninfected monocytes across the BBB, as well as their effects on monocytes/macrophages, microglia, and astrocytes within the CNS. We will also address how these substances of abuse may contribute to HIV-mediated neuropathogenesis in the context of suppressive ART. Additionally, we will review the effects of extracellular dopamine, a neurotransmitter that is increased in the CNS by substances of abuse, on HIV neuropathogenesis and how this may contribute to neuroinflammation, neuronal insult, and HAND in PLWH with active substance use. Lastly, we will discuss some potential therapies to limit CNS inflammation and damage in HIV-infected substance abusers.
全球约有 3700 万人感染人类免疫缺陷病毒(HIV)。HIV 感染的一个非常重要的并发症是,在感染 HIV 的人群(PLWH)中,有 15-55%会发展为 HIV 相关神经认知障碍(HAND),即使在抗逆转录病毒治疗(ART)时代也是如此。HIV 进入中枢神经系统(CNS)发生在外周感染后 4-8 天内。这就建立了病毒储存库,即使在 ART 存在的情况下也可能持续存在。一旦进入 CNS,HIV 就会感染常驻巨噬细胞、小胶质细胞,以及在较低水平下的星形胶质细胞。针对 CNS 内的慢性感染和细胞激活,病毒蛋白、炎症介质以及宿主和病毒神经毒性因子在较长时间内产生,导致神经元损伤和丧失、认知缺陷和 HAND。物质滥用是 PLWH 的常见合并症,已被证明会增加神经炎症和认知障碍。此外,它与 ART 依从性差以及脑脊液(CSF)中病毒载量增加有关,这也可能导致神经炎症和神经元损伤增加。研究已经研究了导致 PLWH 神经炎症和神经元损伤的机制,以及滥用物质如何加剧这些影响。这篇综述将重点讨论滥用物质,特别是甲基苯丙胺(冰毒)、可卡因和阿片类药物,如何影响血脑屏障(BBB)的完整性以及感染和未感染 HIV 的单核细胞穿过 BBB 的迁移,以及它们对 CNS 内的单核细胞/巨噬细胞、小胶质细胞和星形胶质细胞的影响。我们还将讨论这些滥用物质如何在抑制性 ART 背景下导致 HIV 介导的神经发病机制。此外,我们将回顾滥用物质引起的细胞外多巴胺增加对 HIV 神经发病机制的影响,以及这如何导致活跃物质使用的 PLWH 中的神经炎症、神经元损伤和 HAND。最后,我们将讨论一些限制 HIV 感染物质滥用者 CNS 炎症和损伤的潜在治疗方法。