Jensen Brigid K, Monnerie Hubert, Mannell Maggie V, Gannon Patrick J, Espinoza Cagla Akay, Erickson Michelle A, Bruce-Keller Annadora J, Gelman Benjamin B, Briand Lisa A, Pierce R Christopher, Jordan-Sciutto Kelly L, Grinspan Judith B
From the Department of Neuroscience, The Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania (BKJ, MVM); Department of Neurology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania (BKJ, HM, JBG); Department of Pathology, School of Dental Medicine, University of Pennsylvania, Philadelphia, Pennsylvania (BKJ, PJG, CAE, MAE, KLJ-S); Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, Louisiana (AJB-K); Department of Pathology, University of Texas Medical Branch, Galveston, Texas (BBG) Department of Psychology, College of Liberal Arts, Temple University, Philadelphia, Pennsylvania (LAB); Center for Neurobiology and Behavior, Department of Psychiatry, The Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania (CP).
J Neuropathol Exp Neurol. 2015 Nov;74(11):1093-118. doi: 10.1097/NEN.0000000000000255.
Despite effective viral suppression through combined antiretroviral therapy (cART), approximately half of HIV-positive individuals have HIV-associated neurocognitive disorders (HAND). Studies of antiretroviral-treated patients have revealed persistent white matter abnormalities including diffuse myelin pallor, diminished white matter tracts, and decreased myelin protein mRNAs. Loss of myelin can contribute to neurocognitive dysfunction because the myelin membrane generated by oligodendrocytes is essential for rapid signal transduction and axonal maintenance. We hypothesized that myelin changes in HAND are partly due to effects of antiretroviral drugs on oligodendrocyte survival and/or maturation. We showed that primary mouse oligodendrocyte precursor cell cultures treated with therapeutic concentrations of HIV protease inhibitors ritonavir or lopinavir displayed dose-dependent decreases in oligodendrocyte maturation; however, this effect was rapidly reversed after drug removal. Conversely, nucleoside reverse transcriptase inhibitor zidovudine had no effect. Furthermore, in vivo ritonavir administration to adult mice reduced frontal cortex myelin protein levels. Finally, prefrontal cortex tissue from HIV-positive individuals with HAND on cART showed a significant decrease in myelin basic protein compared with untreated HIV-positive individuals with HAND or HIV-negative controls. These findings demonstrate that antiretrovirals can impact myelin integrity and have implications for myelination in juvenile HIV patients and myelin maintenance in adults on lifelong therapy.
尽管通过联合抗逆转录病毒疗法(cART)实现了有效的病毒抑制,但大约一半的HIV阳性个体患有与HIV相关的神经认知障碍(HAND)。对抗逆转录病毒治疗患者的研究发现了持续的白质异常,包括弥漫性髓鞘苍白、白质束减少以及髓鞘蛋白mRNA水平降低。髓鞘的丧失会导致神经认知功能障碍,因为少突胶质细胞产生的髓鞘膜对于快速信号转导和轴突维持至关重要。我们假设HAND中的髓鞘变化部分归因于抗逆转录病毒药物对少突胶质细胞存活和/或成熟的影响。我们发现,用治疗浓度的HIV蛋白酶抑制剂利托那韦或洛匹那韦处理的原代小鼠少突胶质细胞前体细胞培养物中,少突胶质细胞成熟呈现剂量依赖性降低;然而,在去除药物后这种效应迅速逆转。相反,核苷类逆转录酶抑制剂齐多夫定没有效果。此外,对成年小鼠进行体内利托那韦给药会降低额叶皮质的髓鞘蛋白水平。最后,与未接受治疗的HAND HIV阳性个体或HIV阴性对照相比,接受cART治疗且患有HAND的HIV阳性个体的前额叶皮质组织中髓鞘碱性蛋白显著减少。这些发现表明抗逆转录病毒药物会影响髓鞘完整性,对青少年HIV患者的髓鞘形成以及接受终身治疗的成年人的髓鞘维持具有重要意义。