In Vivo Models of Human Immunodeficiency Virus Persistence and Cure Strategies

被引:32
作者
Nixon, Christopher C. [1 ]
Mavigner, Maud [2 ]
Silvestri, Guido [3 ,4 ]
Garcia, J. Victor [1 ]
机构
[1] Univ North Carolina Chapel Hill, Sch Med, Ctr AIDS Res, Div Infect Dis, CB 7042,Genet Med Bldg,120 Mason Farm Rd, Chapel Hill, NC 27599 USA
[2] Emory Univ, Sch Med, Dept Pediat, Atlanta, GA USA
[3] Emory Univ, Emory Vaccine Ctr, Atlanta, GA 30322 USA
[4] Emory Univ, Yerkes Natl Primate Res Ctr, Atlanta, GA 30322 USA
基金
美国国家卫生研究院;
关键词
HIV latency; AIDS; humanized mice; animal models; non-human primates; BROADLY NEUTRALIZING ANTIBODIES; T-CELL DEPLETION; ACTIVE ANTIRETROVIRAL THERAPY; FOLLICULAR DENDRITIC CELLS; INFECTED RHESUS MACAQUES; PRIMARY HIV-1 INFECTION; IMMUNE-RESPONSES; VIRAL RESERVOIRS; NEUROCOGNITIVE IMPAIRMENT; REPLICATION-COMPETENT;
D O I
10.1093/infdis/jiw637
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Current HIV therapy is not curative regardless of how soon after infection it is initiated or how long it is administered, and therapy interruption almost invariably results in robust viral rebound. Human immunodeficiency virus persistence is therefore the major obstacle to a cure for AIDS. The testing and implementation of novel yet unproven approaches to HIV eradication that could compromise the health status of HIV-infected individuals might not be ethically warranted. Therefore, adequate in vitro and in vivo evidence of efficacy is needed to facilitate the clinical implementation of promising strategies for an HIV cure. Animal models of HIV infection have a strong and well-documented history of bridging the gap between laboratory discoveries and eventual clinical implementation. More recently, animal models have been developed and implemented for the in vivo evaluation of novel HIV cure strategies. In this article, we review the recent progress in this rapidly moving area of research, focusing on the two most promising model systems: humanized mice and nonhuman primates.
引用
收藏
页码:S142 / S151
页数:10
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