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Transplantation of human umbilical cord blood CD34 cells into the liver of newborn NOD/SCID/IL-2Rγ null (NSG) mice after busulfan conditioning.在白消安预处理后,将人脐带血CD34细胞移植到新生NOD/SCID/IL-2Rγ基因敲除(NSG)小鼠的肝脏中。
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Brain Invasion by CD4(+) T Cells Infected with a Transmitted/Founder HIV-1BJZS7 During Acute Stage in Humanized Mice.在人源化小鼠的急性感染期,感染传播/原始 HIV-1BJZS7 的 CD4(+)T 细胞侵犯大脑。
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利用人源化小鼠模型研究HIV-1感染、发病机制及持续性

Use of Humanized Mouse Models for Studying HIV-1 Infection, Pathogenesis and Persistence.

作者信息

Weichseldorfer Matthew, Heredia Alonso, Reitz Marvin, Bryant Joseph L, Latinovic Olga S

机构信息

Institute of Human Virology, School of Medicine, University of Maryland, Baltimore, United States.

Department of Medicine, School of Medicine, University of Maryland, Baltimore, United States.

出版信息

J AIDS HIV Treat. 2020;2(1):23-29.

PMID:32457941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7250391/
Abstract

Despite decades of intensive basic and clinical research efforts, there is still no successful vaccine candidate against human immunodeficiency virus (HIV-1). Standard combined antiretroviral therapy (cART) has been successfully developed and has given remarkable results suppressing HIV-1 infection and transmission. However, cART cannot fully clear the virus from the infected patients. A cure for HIV-1 is highly desirable to stop both the spread of the virus in humans and disease progression in HIV-1 patients. A safe and effective cure strategy for HIV-1 infection will require appropriate animal models that properly mimic HIV-1 infection and advance HIV-1 cure research. Animal models have been a crucial tool in the drug discovery process for investigation of HIV-1 disease mainly in preclinical evaluations of antiretroviral drugs and vaccines. An ideal animal model should recapitulate the main aspects of human-specific HIV-1 infection and pathogenesis with their associated immune responses, while permitting invasive antiretroviral studies. The best humanized mouse models would allow a thorough evaluation of antiretroviral strategies that are aimed towards reducing the establishment and size of the HIV-1 reservoirs. In this review, we evaluate multiple humanized mouse models while presenting their strengths and limitations for HIV-1 research. These humanized mouse models have been tailored in recent decades and heavily employed to address specific quintessential and remaining questions of HIV-1 persistence, pathogenesis and ultimately, eradication.

摘要

尽管经过了数十年深入的基础和临床研究努力,但仍然没有成功的抗人类免疫缺陷病毒(HIV-1)疫苗候选物。标准的联合抗逆转录病毒疗法(cART)已成功开发,并在抑制HIV-1感染和传播方面取得了显著成果。然而,cART无法将病毒从感染患者体内完全清除。治愈HIV-1对于阻止病毒在人类中的传播以及HIV-1患者的疾病进展极为重要。一种安全有效的HIV-1感染治愈策略将需要合适的动物模型,这些模型能够恰当地模拟HIV-1感染并推动HIV-1治愈研究。动物模型一直是HIV-1疾病药物发现过程中的关键工具,主要用于抗逆转录病毒药物和疫苗的临床前评估。理想的动物模型应概括人类特异性HIV-1感染和发病机制的主要方面及其相关免疫反应,同时允许进行侵入性抗逆转录病毒研究。最佳的人源化小鼠模型将允许对旨在减少HIV-1储存库的建立和规模的抗逆转录病毒策略进行全面评估。在本综述中,我们评估了多种人源化小鼠模型,同时阐述了它们在HIV-1研究中的优势和局限性。近几十年来,这些人源化小鼠模型经过了定制,并大量用于解决HIV-1持续存在、发病机制以及最终根除方面的特定关键和遗留问题。