Banks Wiliam A, Ercal Nuran, Price Tulin Otamis
Geriatric Research Education and Clinical Center, Veterans Affairs Medical Center-St. Louis, St. Louis, MO 63106, USA.
Curr HIV Res. 2006 Jul;4(3):259-66. doi: 10.2174/157016206777709447.
Nearly every aspect of blood-brain barrier (BBB) function is involved in or affected by HIV-1. The disruption of the BBB tends to be minimal and is not likely the mechanism by which infected immune cells and virus enter the brain. Instead, immune cells, virus and viral proteins likely activate brain endothelial cells and enable their own passage across the BBB by way of highly regulated processes such as diapedesis and adsorptive endocytosis. Viral proteins and cytokines can enter the CNS from the blood and provide a mechanism by which HIV-1 can affect CNS function independent of viral transport. Brain endothelial cells can also secrete neuroimmunoactive substances when stimulated by HIV-1, gp120, and Tat. Efflux systems such as p-glycoprotein transport anti-virals in the brain-to-blood direction, thus hampering effective accumulation of drug by the CNS. Overall, the BBB plays a major role in establishing and maintaining virus within the CNS and neuroAIDS.
血脑屏障(BBB)功能的几乎每个方面都与HIV-1相关或受其影响。血脑屏障的破坏往往很小,不太可能是受感染的免疫细胞和病毒进入大脑的机制。相反,免疫细胞、病毒和病毒蛋白可能会激活脑内皮细胞,并通过诸如渗出和吸附性胞吞作用等高度调控的过程使其自身穿过血脑屏障。病毒蛋白和细胞因子可从血液进入中枢神经系统,并提供一种机制,使HIV-1能够独立于病毒转运而影响中枢神经系统功能。当受到HIV-1、gp120和Tat刺激时,脑内皮细胞也可分泌神经免疫活性物质。诸如P-糖蛋白等外排系统将抗病毒药物从脑内向血液方向转运,从而阻碍中枢神经系统有效蓄积药物。总体而言,血脑屏障在中枢神经系统内病毒的建立和维持以及神经艾滋病中起主要作用。
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