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用于评估 HIV 治愈策略的临床前评价的人源化小鼠模型。

Humanized mouse models for preclinical evaluation of HIV cure strategies.

机构信息

Institute of Human Virology, University of Maryland School of Medicine, Baltimore, Maryland, USA.

出版信息

AIDS Rev. 2022 Oct 25;24(3):139-151. doi: 10.24875/AIDSRev.22000013.

Abstract

Although the world is currently focused on the COVID-19 pandemic, HIV/AIDS remains a significant threat to public health. To date, the HIV/AIDS pandemic has claimed the lives of over 36 million people, while nearly 38 million people are currently living with the virus. Despite the undeniable success of antiretroviral therapy (ART) in controlling HIV, the medications are not curative. Soon after initial infection, HIV integrates into the genome of infected cells as a provirus, primarily, within CD4+ T lymphocytes and tissue macrophages. When not actively transcribed, the provirus is referred to as a latent reservoir because it is hidden to the immune system and ART. Following ART discontinuation, HIV may emerge from the replication-competent proviruses and resumes the infection of healthy cells. Thus, these latent reservoirs are a major obstacle to an HIV cure, and their removal remains a priority. A vital aspect in the development of curative therapies is the demonstration of efficacy in an animal model, such as the humanized mouse model. Therefore, optimization, standardization, and validation of the humanized mouse model are a priority. The purpose of this review article is to provide an update on existing humanized mouse models, highlighting the advantages and disadvantages of each as they pertain to HIV cure studies and to review the approaches to curative therapies that are under investigation.

摘要

尽管世界目前专注于 COVID-19 大流行,但艾滋病毒/艾滋病仍然是对公共卫生的重大威胁。迄今为止,艾滋病毒/艾滋病大流行已夺走了 3600 多万人的生命,而目前近 3800 万人携带该病毒。尽管抗逆转录病毒疗法 (ART) 在控制艾滋病毒方面取得了不可否认的成功,但这些药物并不能治愈疾病。在初始感染后不久,HIV 就会作为前病毒整合到受感染细胞的基因组中,主要是在 CD4+T 淋巴细胞和组织巨噬细胞中。当不进行主动转录时,前病毒被称为潜伏储库,因为它对免疫系统和 ART 是隐藏的。ART 停药后,HIV 可能从前病毒复制能力中出现并恢复感染健康细胞。因此,这些潜伏储库是实现 HIV 治愈的主要障碍,清除它们仍然是当务之急。在开发治愈性疗法方面,一个重要方面是在动物模型中证明疗效,例如人源化小鼠模型。因此,优化、标准化和验证人源化小鼠模型是当务之急。本文的目的是提供对现有人类化小鼠模型的更新,强调每种模型在 HIV 治愈研究中的优缺点,并回顾正在研究的治愈性治疗方法。

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