Jazebi Noushin, Evans Chad, Kadaru Hima S, Kompella Divya, Raji Mukaila, Fang Felix, Pappolla Miguel, Tang Shao-Jun, Chung Jin Mo, Hammock Bruce, Fang Xiang
Department of Neurology, University of Texas Medical Branch, Galveston, TX 77555.
Department of Medicine, University of Texas Medical Branch, Galveston, TX 77555.
J Neurol Exp Neurosci. 2021;7(1):15-24. doi: 10.17756/jnen.2021-082. Epub 2021 Feb 6.
HIV-sensory neuropathy (HIV-SN) is a debilitating complication in HIV patients with or without anti-retroviral treatment (ART). Common symptoms of HIV-SN include pain, decreased sensation, paresthesias, and dysesthesias in a symmetric stocking-glove distribution. While HIV-1 protein such as gp120 is implicated in HIV-SN (e.g. impaired large-diameter fiber), ART itself was recently shown to contribute to HIV-SN in HIV patients and impair thin fiber. Multiple host mechanisms may play roles during the pathogenesis of HIV-SN, including neuron-glia interactions in the spinal dorsal horn (SDH), inflammation, mitochondrial dysfunction and endoplasmic reticulum stress. Concurrent infections, such as tuberculosis, also carry a higher likelihood of HIV-SN as well as environmental or genetic predisposition. Pro-inflammatory cytokines such as IL-1, IL2 receptor-alpha, and tumor necrosis factor (TNF) along with abnormal lactate levels have been identified as potential players within the complex pathophysiology of this condition. In this paper, we review the pathophysiology of HIV neuropathy, focusing on the various treatment options available or under investigation. Although several treatment options are available e.g., the capsaicin patch and spinal cord stimulation, symptomatic control of HIV-SN are often challenging. Alternative approaches such as self-hypnosis, resistance exercise, cannabinoids, and acupuncture have all shown promising results, but need further investigation.
HIV 感觉神经病变(HIV-SN)是接受或未接受抗逆转录病毒治疗(ART)的 HIV 患者中一种使人衰弱的并发症。HIV-SN 的常见症状包括疼痛、感觉减退、感觉异常和感觉障碍,呈对称的袜套样和手套样分布。虽然 HIV-1 蛋白如 gp120 与 HIV-SN 有关(如大直径纤维受损),但最近研究表明,ART 本身也会导致 HIV 患者出现 HIV-SN 并损害细纤维。多种宿主机制可能在 HIV-SN 的发病过程中起作用,包括脊髓背角(SDH)中的神经元-神经胶质细胞相互作用、炎症、线粒体功能障碍和内质网应激。并发感染,如结核病,也更有可能引发 HIV-SN,还有环境或遗传易感性因素。促炎细胞因子如白细胞介素-1、白细胞介素-2 受体α和肿瘤坏死因子(TNF)以及异常的乳酸水平已被确定为这种疾病复杂病理生理学中的潜在因素。在本文中,我们综述了 HIV 神经病变的病理生理学,重点关注现有的或正在研究的各种治疗选择。尽管有几种治疗选择,如辣椒素贴片和脊髓刺激,但对 HIV-SN 进行症状控制往往具有挑战性。自我催眠、阻力运动、大麻素和针灸等替代方法都显示出了有希望的结果,但还需要进一步研究。