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[小鼠并非人类,但……人源化小鼠如何让我们了解人类传染病]

[Mice are not Men and yet… how humanized mice inform us about human infectious diseases].

作者信息

Cachat Anne, Villaudy Julien, Rigal Dominique, Gazzolo Louis, Duc Dodon Madeleine

机构信息

Virologie humaine, INSERM-U758, École Normale Supérieure, France.

出版信息

Med Sci (Paris). 2012 Jan;28(1):63-8. doi: 10.1051/medsci/2012281018. Epub 2012 Jan 27.

Abstract

The study of human pathologies is often limited by the absence of animal models which are robust, cost-effective and reproduce the hallmarks of human infections. While mice have been frequently employed to study human diseases, many of important pathogens display unique human tropism. These last two decades the graft of human progenitor cells or tissues into -immunodeficient mice has allowed the elaboration of so called humanized mice. Humanized mouse technology has made rapid progress, and it is now possible to achieve high levels of human chimerism in various organs and tissues, particularly the immune system and the liver. The review briefly summarizes the different models of humanized mice available for in vivo experiments. With a focus on lymphotropic, monocytotropic and hepatotropic viruses, we here discuss the current status and future prospects of these models for studying the pathogenesis of infectious diseases. Furthermore, they provide a powerful tool for the development of innovative therapies.

摘要

人类病理学的研究常常受到缺乏动物模型的限制,这些动物模型需要具备强健性、成本效益且能重现人类感染的特征。虽然小鼠经常被用于研究人类疾病,但许多重要病原体表现出独特的人类嗜性。在过去二十年中,将人类祖细胞或组织移植到免疫缺陷小鼠体内使得所谓的人源化小鼠得以构建。人源化小鼠技术取得了快速进展,现在有可能在各种器官和组织,特别是免疫系统和肝脏中实现高水平的人类嵌合现象。本文简要总结了可用于体内实验的不同人源化小鼠模型。重点关注嗜淋巴细胞、嗜单核细胞和嗜肝病毒,我们在此讨论这些模型在研究传染病发病机制方面的现状和未来前景。此外,它们为创新疗法的开发提供了强大工具。

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