Compartmentalization, Viral Evolution, and Viral Latency of HIV in the CNS

被引:80
作者
Bednar, Maria M. [1 ]
Sturdevant, Christa Buckheit [2 ]
Tompkins, Lauren A. [3 ]
Arrildt, Kathryn Twigg [3 ]
Dukhovlinova, Elena [1 ]
Kincer, Laura P. [1 ]
Swanstrom, Ronald [1 ,3 ,4 ]
机构
[1] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[2] Duke Univ, Med Ctr, Dept Surg, Durham, NC 27710 USA
[3] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Dept Biochem & Biophys, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
关键词
Human immunodeficiency virus; HIV; Compartmentalization; Tropism; Latency; Evolution; Eradication; CNS; CSF; Animal models; HUMAN-IMMUNODEFICIENCY-VIRUS; CENTRAL-NERVOUS-SYSTEM; SYNCYTIUM-INDUCING PHENOTYPE; ENHANCES MACROPHAGE TROPISM; FEMALE GENITAL-TRACT; T-CELL SUBSETS; CEREBROSPINAL-FLUID; ADAPTIVE EVOLUTION; IN-VIVO; TYPE-1;
D O I
10.1007/s11904-015-0265-9
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Human immunodeficiency virus type 1 (HIV-1) infection occurs throughout the body and can have dramatic physical effects, such as neurocognitive impairment in the central nervous system (CNS). Furthermore, examining the virus that resides in the CNS is challenging due to its location and can only be done using samples collected either at autopsy, indirectly form the cerebral spinal fluid (CSF), or through the use of animal models. The unique milieu of the CNS fosters viral compartmentalization as well as evolution of viral sequences, allowing for new cell types, such as macrophages and microglia, to be infected. Treatment must also cross the blood-brain barrier adding additional obstacles in eliminating viral populations in the CNS. These long-lived infected cell types and treatment barriers may affect functional cure strategies in people on highly active antiretroviral therapy (HAART).
引用
收藏
页码:262 / 271
页数:10
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