Laboratorio Inmunobiología Molecular, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Rev Med Virol. 2012 Jan;22(1):33-45. doi: 10.1002/rmv.711. Epub 2011 Sep 23.
Brain HIV-1-infection may result in a syndrome of profound cognitive, behavioral and motor impairment known as AIDS dementia complex (ADC) in adults and HIV-related encephalopathy in children. Although the introduction of highly active antiretroviral therapy (HAART) has prolonged and improved the lives of infected individuals, it is clear that HAART does not provide complete protection against neurological damage in HIV/AIDS. HIV-1 associated dementia is a complex phenomenon, which could be the result of several mechanisms caused by those players using different intracellular signaling pathways. Understanding the causes of neurodegeneration during HIV-1 infection and the factors which certain individuals develop disease can provide researches on new therapeutic targets to positively affect disease outcomes. Controlling CNS viral replication with HAART is an essential primary approach, but it should be complemented with adjunctive CNS-directed therapeutics. Understanding the nature of HIV-1 infection within the CNS as well as inflammatory responses will ultimately lead to the elimination of HIV-associated neurocognitive disorders.
脑 HIV-1 感染可能导致一种严重的认知、行为和运动障碍综合征,在成人中称为艾滋病痴呆综合征 (ADC),在儿童中称为与 HIV 相关的脑病。尽管高效抗逆转录病毒疗法 (HAART) 的引入延长并改善了感染者的生命,但显然 HAART 并不能完全防止 HIV/AIDS 中的神经损伤。HIV-1 相关痴呆是一种复杂的现象,可能是由多种机制引起的,这些机制涉及到使用不同细胞内信号通路的参与者。了解 HIV-1 感染期间神经退行性变的原因以及某些个体发生疾病的因素,可以为新的治疗靶点提供研究,从而对疾病结果产生积极影响。用 HAART 控制中枢神经系统病毒复制是一种基本的主要方法,但应辅以中枢神经系统靶向的辅助治疗。了解 HIV-1 在中枢神经系统内的感染特性以及炎症反应,最终将导致消除与 HIV 相关的神经认知障碍。