Potential pharmacological approaches for the treatment of HIV-1 associated neurocognitive disorders

被引:21
|
作者
Omeragic, Amila [1 ]
Kayode, Olanre [1 ]
Hoque, Md Tozammel [1 ]
Bendayan, Reina [1 ]
机构
[1] Univ Toronto, Leslie Dan Fac Pharm, Dept Pharmaceut Sci, 144 Coll St,Room 1001, Toronto, ON M5S 3M2, Canada
基金
加拿大健康研究院;
关键词
HIV-1; Microglia; Astrocytes; Neurons; Inflammation; Blood-brain barrier; Cytokine; IMMUNODEFICIENCY-VIRUS TYPE-1; CENTRAL-NERVOUS-SYSTEM; MULTINUCLEATED GIANT-CELLS; ACTIVATED-RECEPTOR-GAMMA; BLOOD-BRAIN-BARRIER; AIDS DEMENTIA COMPLEX; MESSENGER-RNA ACCUMULATION; TAT-INDUCED ALTERATIONS; TRANSGENIC RAT MODEL; T-LYMPHOTROPIC VIRUS;
D O I
10.1186/s12987-020-00204-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
HIV associated neurocognitive disorders (HAND) are the spectrum of cognitive impairments present in patients infected with human immunodeficiency virus type 1 (HIV-1). The number of patients affected with HAND ranges from 30 to 50% of HIV infected individuals and although the development of combinational antiretroviral therapy (cART) has improved longevity, HAND continues to pose a significant clinical problem as the current standard of care does not alleviate or prevent HAND symptoms. At present, the pathological mechanisms contributing to HAND remain unclear, but evidence suggests that it stems from neuronal injury due to chronic release of neurotoxins, chemokines, viral proteins, and proinflammatory cytokines secreted by HIV-1 activated microglia, macrophages and astrocytes in the central nervous system (CNS). Furthermore, the blood-brain barrier (BBB) not only serves as a route for HIV-1 entry into the brain but also prevents cART therapy from reaching HIV-1 brain reservoirs, and therefore could play an important role in HAND. The goal of this review is to discuss the current data on the epidemiology, pathology and research models of HAND as well as address the potential pharmacological treatment approaches that are being investigated.
引用
收藏
页数:30
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