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研究 HIV 发病机制和治疗的非 BLT 人源化小鼠模型的展望。

Perspectives on Non-BLT Humanized Mouse Models for Studying HIV Pathogenesis and Therapy.

机构信息

Research Center for Drug and Vaccine Development, National Institute of Infectious Diseases, Tokyo 162-8640, Japan.

Department of Life Science and Medical Bioscience, Waseda University, Tokyo 162-8480, Japan.

出版信息

Viruses. 2021 Apr 28;13(5):776. doi: 10.3390/v13050776.

Abstract

A variety of humanized mice, which are reconstituted only with human hematopoietic stem cells (HSC) or with fetal thymus and HSCs, have been developed and widely utilized as in vivo animal models of HIV-1 infection. The models represent some aspects of HIV-mediated pathogenesis in humans and are useful for the evaluation of therapeutic regimens. However, there are several limitations in these models, including their incomplete immune responses and poor distribution of human cells to the secondary lymphoid tissues. These limitations are common in many humanized mouse models and are critical issues that need to be addressed. As distinct defects exist in each model, we need to be cautious about the experimental design and interpretation of the outcomes obtained using humanized mice. Considering this point, we mainly characterize the current conventional humanized mouse reconstituted only with HSCs and describe past achievements in this area, as well as the potential contributions of the humanized mouse models for the study of HIV pathogenesis and therapy. We also discuss the use of various technologies to solve the current problems. Humanized mice will contribute not only to the pre-clinical evaluation of anti-HIV regimens, but also to a deeper understanding of basic aspects of HIV biology.

摘要

已经开发并广泛应用了多种仅用人造血干细胞(HSC)或胎儿胸腺和 HSC 重建的人源化小鼠,作为 HIV-1 感染的体内动物模型。这些模型代表了 HIV 介导的发病机制在人类中的某些方面,可用于评估治疗方案。然而,这些模型存在一些局限性,包括不完全的免疫反应和人类细胞向次级淋巴组织的分布不良。这些局限性在许多人源化小鼠模型中都存在,是需要解决的关键问题。由于每个模型都存在明显的缺陷,因此我们需要谨慎设计实验,并解释使用人源化小鼠获得的结果。考虑到这一点,我们主要描述了目前仅用人 HSC 重建的常规人源化小鼠,并描述了该领域的过去成就,以及人源化小鼠模型在 HIV 发病机制和治疗研究中的潜在贡献。我们还讨论了使用各种技术来解决当前的问题。人源化小鼠不仅将有助于抗 HIV 方案的临床前评估,还将有助于更深入地了解 HIV 生物学的基本方面。

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