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人源化小鼠的传染病。

Infectious diseases in humanized mice.

机构信息

Department of Viral Immunobiology, Institute of Experimental Immunology, University of Zurich, Zurich, Switzerland.

出版信息

Eur J Immunol. 2013 Sep;43(9):2246-54. doi: 10.1002/eji.201343815.

Abstract

Despite many theoretical incompatibilities between mouse and human cells, mice with reconstituted human immune system components contain nearly all human leukocyte populations. Accordingly, several human-tropic pathogens have been investigated in these in vivo models of the human immune system, including viruses such as human immunodeficiency virus (HIV) and Epstein-Barr virus (EBV), as well as bacteria such as Mycobacterium tuberculosis and Salmonella enterica Typhi. While these studies initially aimed to establish similarities in the pathogenesis of infections between these models and the pathobiology in patients, recent investigations have provided new and interesting functional insights into the protective value of certain immune compartments and altered pathology upon mutant pathogen infections. As more tools and methodologies are developed to make these models more versatile to study human immune responses in vivo, such improvements build toward small animal models with human immune components, which could predict immune responses to therapies and vaccination in human patients.

摘要

尽管小鼠和人类细胞之间存在许多理论上的不兼容性,但具有重建的人类免疫系统成分的小鼠几乎包含所有人类白细胞群体。因此,已经在这些人类免疫系统的体内模型中研究了几种人类病原体,包括病毒如人类免疫缺陷病毒 (HIV) 和爱泼斯坦-巴尔病毒 (EBV),以及细菌如结核分枝杆菌和伤寒沙门氏菌。虽然这些研究最初旨在确定这些模型与患者的感染发病机制之间的相似性,但最近的研究为某些免疫区室的保护价值以及突变病原体感染时改变的病理学提供了新的有趣的功能见解。随着更多的工具和方法被开发出来,使这些模型更具体内研究人类免疫反应的多功能性,这些改进将朝着具有人类免疫成分的小型动物模型发展,这些模型可以预测人类患者对治疗和疫苗接种的免疫反应。

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