Department of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, NE 68198-5800, USA.
Biomark Med. 2009 Dec;3(6):771-85. doi: 10.2217/bmm.09.63.
HIV-1 enters the brain shortly after infection, which may lead to neurological complications and in the most severe cases to encephalitis, dementia and death. The introduction of antiretroviral therapy reduced the incidence of the most severe conditions, nevertheless, approximately half of those infected with this virus will suffer to various degrees from HIV-1-associated neurocognitive disorders. Despite many years of research, there are no biomarkers that can objectively measure and, more importantly, predict the onset and the tempo of HIV-1-associated neurocognitive disorders. Here we review biomarker candidates of neurocognitive impairment due to HIV infection of the brain that have been proposed during the last two decades, and discuss perspectives and limitations of proteomic approaches in the search for new, more sensitive and specific biomarkers.
HIV-1 在感染后不久就会进入大脑,这可能导致神经并发症,在最严重的情况下会导致脑炎、痴呆和死亡。抗逆转录病毒疗法的引入降低了最严重情况的发病率,但尽管如此,仍有约一半感染该病毒的人将不同程度地遭受 HIV-1 相关神经认知障碍的困扰。尽管进行了多年的研究,但仍没有能够客观衡量的生物标志物,更重要的是,没有能够预测 HIV-1 相关神经认知障碍的发病和进展速度的生物标志物。在这里,我们回顾了过去二十年中提出的与 HIV 感染大脑导致的神经认知障碍相关的生物标志物候选物,并讨论了蛋白质组学方法在寻找新的、更敏感和更特异的生物标志物方面的前景和局限性。