Section of Infections of the Nervous System, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892-1296, USA.
Dis Model Mech. 2012 May;5(3):313-22. doi: 10.1242/dmm.008763. Epub 2012 Mar 22.
It is well established that infection with the human immunodeficiency virus (HIV) leads to immune suppression. Less well known is the fact that long-term, progressive HIV disease is associated with the development of cognitive deficits. Since the introduction of combined antiretroviral therapy (cART), the clinical presentation of HIV infection has evolved into a chronic illness with very low levels of viral replication and chronic immune activation, with compliant affected individuals surviving for decades with a high quality of life. Despite these advances, many HIV-infected individuals develop some degree of neurodegeneration and cognitive impairment. The underlying pathophysiological mechanisms are not well understood, and there are no effective treatments. Thus, there is an unmet need for animal models that enable the study of HIV-associated neurocognitive disorders (HAND) and the testing of new therapeutic approaches to combat them. Here, we review the pros and cons of existing mouse models of HIV infection for addressing these aims and propose a detailed strategy for developing a new mouse model of HIV infection.
众所周知,人类免疫缺陷病毒(HIV)感染会导致免疫抑制。但鲜为人知的是,长期、进行性的 HIV 疾病与认知缺陷的发展有关。自从联合抗逆转录病毒疗法(cART)问世以来,HIV 感染的临床表现已演变为一种慢性疾病,病毒复制水平极低且慢性免疫激活,符合条件的受影响个体可存活数十年,生活质量很高。尽管取得了这些进展,但许多 HIV 感染者仍会出现一定程度的神经退行性变和认知障碍。其潜在的病理生理机制尚不清楚,也没有有效的治疗方法。因此,需要开发能够研究 HIV 相关神经认知障碍(HAND)并测试新的治疗方法来对抗这些障碍的动物模型。在这里,我们回顾了现有的 HIV 感染小鼠模型在解决这些问题方面的优缺点,并提出了一种开发新型 HIV 感染小鼠模型的详细策略。