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Impacts of Humanized Mouse Models on the Investigation of HIV-1 Infection: Illuminating the Roles of Viral Accessory Proteins in Vivo

机译:人性化的小鼠模型对HIV-1感染调查的影响:阐明体内病毒辅助蛋白的作用

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摘要

Human immunodeficiency virus type 1 (HIV-1) encodes four accessory genes: vif, vpu, vpr, and nef. Recent investigations using in vitro cell culture systems have shed light on the roles of these HIV-1 accessory proteins, Vif, Vpr, Vpu, and Nef, in counteracting, modulating, and evading various cellular factors that are responsible for anti-HIV-1 intrinsic immunity. However, since humans are the exclusive target for HIV-1 infection, conventional animal models are incapable of mimicking the dynamics of HIV-1 infection in vivo. Moreover, the effects of HIV-1 accessory proteins on viral infection in vivo remain unclear. To elucidate the roles of HIV-1 accessory proteins in the dynamics of viral infection in vivo, humanized mouse models, in which the mice are xenotransplanted with human hematopoietic stem cells, has been utilized. This review describes the current knowledge of the roles of HIV-1 accessory proteins in viral infection, replication, and pathogenicity in vivo, which are revealed by the studies using humanized mouse models.
机译:1型人类免疫缺陷病毒(HIV-1)编码四个辅助基因:vif,vpu,vpr和nef。最近使用体外细胞培养系统进行的研究揭示了这些HIV-1辅助蛋白Vif,Vpr,Vpu和Nef在抵消,调节和逃避引起抗HIV-1的各种细胞因子方面的作用。固有免疫力。但是,由于人类是HIV-1感染的唯一目标,因此常规动物模型无法模仿HIV-1体内感染的动态。此外,HIV-1辅助蛋白对体内病毒感染的影响仍不清楚。为了阐明HIV-1辅助蛋白在体内病毒感染动力学中的作用,已经使用了人源化小鼠模型,在该模型中,小鼠被异种了人类造血干细胞。这篇综述描述了关于HIV-1辅助蛋白在体内病毒感染,复制和致病性中的作用的最新知识,这些发现通过使用人源化小鼠模型的研究得以揭示。

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