急性HIV感染的神经系统并发症。

Kathryn B Holroyd, Anastasia Vishnevetsky, Maahika Srinivasan, Deanna Saylor
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引用次数: 8

摘要

综述目的:本文综述了急性HIV感染(AHI)的病理生理和相关的中枢神经系统(CNS)病理,AHI神经系统并发症的临床特点,以及CNS储库和病毒逃逸对HIV治疗和治愈策略的影响。最近的发现:最近对新血清转化人群的研究表明,AHI中周围神经病变和认知功能障碍的患病率很高,尽管这些发现通常与慢性HIV感染有关。HIV治疗策略,如“休克和杀伤”策略,目前正在体外甚至小型临床试验中进行研究,尽管中枢神经系统作为潜伏HIV的储存库对这些治疗策略构成了独特的障碍。总结:对AHI的有限的护理点诊断测试和对感染的延迟识别继续导致对AHI神经系统表现的认识不足和报告不足。AHI应作为广泛的神经系统疾病的鉴别指标,从贝尔氏麻痹、周围神经病变和无菌性脑膜炎,到更罕见的表现,如ADEM、AIDP、脑根炎、横脊髓炎和臂神经炎。这些疾病的治疗包括早期开始抗逆转录病毒治疗(ART),然后是标准的针对症状的治疗。目前正在研究的HIV治愈策略包括骨髓移植、病毒库再激活和根除以及基因组和表观遗传病毒靶向。然而,随着CNS病毒库的建立,HIV-1侵入CNS发生在病程的早期,这是这些治疗的重要限制因素。
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Neurologic Complications of Acute HIV Infection.

Purpose of review: This review focuses on the pathophysiology of acute HIV infection (AHI) and related central nervous system (CNS) pathology, the clinical characteristics of neurologic complications of AHI, and the implications of the CNS reservoir and viral escape for HIV treatment and cure strategies.

Recent findings: Recent studies in newly seroconverted populations show a high prevalence of peripheral neuropathy and cognitive dysfunction in AHI, even though these findings have been classically associated with chronic HIV infection. HIV cure strategies such as the "shock and kill" strategy are currently being studied in vitro and even in small clinical trials, though the CNS as a reservoir for latent HIV poses unique barriers to these treatment strategies.

Summary: Limited point of care diagnostic testing for AHI and delayed recognition of infection continue to lead to under-recognition and under-reporting of neurologic manifestations of AHI. AHI should be on the differential for a broad range of neurological conditions, from Bell's palsy, peripheral neuropathy, and aseptic meningitis, to more rare manifestations such as ADEM, AIDP, meningo-radiculitis, transverse myelitis, and brachial neuritis. Treatment for these conditions involves early initiation of antiretroviral therapy (ART) and then standard presentation-specific treatments. Current HIV cure strategies under investigation include bone marrow transplant, viral reservoir re-activation and eradication, and genome and epigenetic viral targeting. However, CNS penetration by HIV-1 occurs early on in the disease course with the establishment of the CNS viral reservoir and is an important limiting factor for these therapies.

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