The utility of nonhuman primate models for understanding acute HIV-1 infection

被引:0
作者
Parsons, Matthew S. [1 ,2 ,3 ]
Bolton, Diane L. [2 ,3 ]
机构
[1] Armed Forces Res Inst Med Sci, Walter Reed Army Inst Res, Bangkok, Thailand
[2] US Mil, HIV Res Program, CIDR, Walter Reed Army Inst Res, Silver Spring, MD USA
[3] Henry M Jackson Fdn Adv Mil Med Inc, Bethesda, MD USA
基金
美国国家卫生研究院;
关键词
acute HIV-1 infection; chronic HIV-1 infection; nonhuman primates; simian immunodeficiency virus; simian-human immunodeficiency virus; CD4(+) T-CELLS; MONOCLONAL-ANTIBODIES; NEUROCOGNITIVE DISORDERS; ANTIRETROVIRAL THERAPY; VIRUS-REPLICATION; DEPLETION; RESERVOIR; RESPONSES; VIREMIA;
D O I
10.1097/COH.0000000000000920
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose of reviewNonhuman primate (NHP) models of HIV-1 infection provide complementary experimental pathways for assessing aspects of acute HIV-1 infection (AHI) that cannot be addressed in humans. This article reviews acute infection studies in SIV-infected or SHIV-infected macaque species over the previous 18 months.Recent findingsReviewed studies examined the dynamics of replication-competent viral reservoir establishment during early infection, reservoir maintenance throughout therapy, and factors influencing viral rebound after treatment cessation. Also discussed are acute infection events in the central nervous system and liver and potential links between these events and manifestations of comorbidities during chronic infection. Additional studies addressed how occurrences during acute infection impact the development of natural viral control or posttreatment control. Another report evaluated treatment during acute infection with broadly neutralizing antibodies with enhanced ability to engage innate immune cells, highlighting the ability of this early intervention to shape innate and adaptive antiviral responses.SummaryNHP models of HIV-1 infection are a fundamental research tool for investigating AHI events. These models enable detailed pathogenesis characterization and the testing of hypothesis-driven strategies for altering disease courses through interventions during AHI, including targeting viral persistence and comorbidities that persist throughout chronic infection.
引用
收藏
页码:218 / 227
页数:10
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