AIDS and Cancer Virus Program, Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA.
Curr Opin HIV AIDS. 2013 Jul;8(4):262-72. doi: 10.1097/COH.0b013e328361cf40.
Animal models will be critical for preclinical evaluations of novel HIV eradication and/or functional cure strategies in the setting of suppressive combination antiretroviral therapy (cART). Here, the strengths, limitations, and challenges of recent efforts to develop nonhuman primate (NHP) models of cART-mediated suppression for use in studies of persistent virus and curative approaches are discussed.
Several combinations of NHP species and viruses that recapitulate key aspects of human HIV infection have been adapted for cART-mediated suppression studies. Different cART regimens incorporating drugs targeting multiple different steps of the viral replication cycle have provided varying levels of virologic suppression, dependent in part upon the host species, virus, drug regimen and timing, and virologic monitoring assay sensitivity. New, increasingly sensitive virologic monitoring approaches for measurements of plasma viral RNA, cell-associated and tissue-associated viral RNA and DNA, and the replication-competent residual viral pool in the setting of cART in NHP models are being developed to allow for the assessment of persistent virus on cART and to evaluate the impact of viral induction/eradication strategies in vivo.
Given the vagaries of each specific virus and host species, and cART regimen, each model will require further development and analysis to determine their appropriate application for addressing specific experimental questions.
综述目的:在抑制性联合抗逆转录病毒疗法(cART)背景下,动物模型对于评估新型 HIV 清除和/或功能性治愈策略的临床前研究至关重要。本文讨论了最近为开发用于持续性病毒和治疗方法研究的 cART 介导抑制的非人类灵长类动物(NHP)模型而做出的努力的优势、局限性和挑战。
最新发现:已经有几种灵长类动物物种和病毒的组合被用于 cART 介导抑制的研究,这些组合再现了人类 HIV 感染的关键方面。不同的 cART 方案包含针对病毒复制周期多个不同步骤的药物,提供了不同程度的病毒学抑制,部分取决于宿主物种、病毒、药物方案和时间以及病毒学监测分析敏感性。新的、越来越敏感的病毒学监测方法正在被开发,用于测量 cART 背景下的血浆病毒 RNA、细胞相关和组织相关病毒 RNA 和 DNA 以及复制性剩余病毒库,以评估 cART 上的持续性病毒,并评估体内病毒诱导/清除策略的影响。
总结:鉴于每种特定病毒和宿主物种以及 cART 方案的复杂性,每个模型都需要进一步开发和分析,以确定其在解决特定实验问题方面的适当应用。