Nath Avi
Department of Neurology, Johns Hopkins University, 600 N. Wolfe Street, Meyer 6-109, Baltimore, MD 21287-7609, USA.
J Infect Dis. 2002 Dec 1;186 Suppl 2:S193-8. doi: 10.1086/344528.
Human immunodeficiency virus (HIV) infection of the nervous system is unique when compared with other viral encephalitides. Neuronal cell loss occurs in the absence of neuronal infection. Viral proteins, termed "virotoxins," are released from the infected glial cells that initiate a cascade of positive feedback loops by activating uninfected microglial cells and astrocytes. These activated cells release a variety of toxic substances that result in neuronal dysfunction and cell loss. The virotoxins act by a hit and run phenomenon. Thus, a transient exposure to the proteins initiates the neurotoxic cascade. High concentrations of these proteins likely occur in tight extracellular spaces where they may cause direct neurotoxicity as well. The emerging concepts in viral protein-induced neurotoxicity are reviewed as are the neurotoxic potential of each protein. Future therapeutic strategies must target common mechanisms such as oxidative stress and dysregulation of intracellular calcium involved in virotoxin-mediated neurotoxicity.
与其他病毒性脑炎相比,人类免疫缺陷病毒(HIV)对神经系统的感染具有独特性。在没有神经元感染的情况下会发生神经元细胞丢失。被称为“病毒毒素”的病毒蛋白从受感染的神经胶质细胞中释放出来,通过激活未感染的小胶质细胞和星形胶质细胞引发一系列正反馈回路。这些活化细胞释放出多种有毒物质,导致神经元功能障碍和细胞丢失。病毒毒素通过“打一枪换一个地方”的现象起作用。因此,对这些蛋白的短暂暴露会引发神经毒性级联反应。这些蛋白的高浓度可能出现在紧密的细胞外空间中,在那里它们也可能导致直接的神经毒性。本文综述了病毒蛋白诱导神经毒性的新观念以及每种蛋白的神经毒性潜力。未来的治疗策略必须针对诸如氧化应激和病毒毒素介导的神经毒性中涉及的细胞内钙失调等共同机制。