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用于研究登革病毒免疫学和发病机制的小鼠模型。

Mouse models to study dengue virus immunology and pathogenesis.

作者信息

Zellweger Raphaël M, Shresta Sujan

机构信息

Division of Vaccine Discovery, La Jolla Institute for Allergy and Immunology , La Jolla, CA , USA.

出版信息

Front Immunol. 2014 Apr 10;5:151. doi: 10.3389/fimmu.2014.00151. eCollection 2014.

Abstract

The development of a compelling murine model of dengue virus (DENV) infection has been challenging, because DENV clinical isolates do not readily replicate or cause pathology in immunocompetent mice. However, research using immunocompromised mice and/or mouse-adapted viruses allows investigation of questions that may be impossible to address in human studies. In this review, we discuss the potential strengths and limitations of existing mouse models of dengue disease. Human studies are descriptive by nature; moreover, the strain, time, and sequence of infection are often unknown. In contrast, in mice, the conditions of infection are well defined and a large number of experimental parameters can be varied at will. Therefore, mouse models offer an opportunity to experimentally test hypotheses that are based on epidemiological observations. In particular, gain-of-function or loss-of-function models can be established to assess how different components of the immune system (either alone or in combination) contribute to protection or pathogenesis during secondary infections or after vaccination. In addition, mouse models have been used for pre-clinical testing of anti-viral drugs or for vaccine development studies. Conclusions based on mouse experiments must be extrapolated to DENV-infection in humans with caution due to the inherent limitations of animal models. However, research in mouse models is a useful complement to in vitro and epidemiological data, and may delineate new areas that deserve attention during future human studies.

摘要

登革病毒(DENV)感染的令人信服的小鼠模型的开发一直具有挑战性,因为DENV临床分离株在免疫健全的小鼠中不易复制或引起病变。然而,使用免疫受损小鼠和/或小鼠适应病毒的研究允许探讨一些在人体研究中可能无法解决的问题。在这篇综述中,我们讨论了现有登革热疾病小鼠模型的潜在优势和局限性。人体研究本质上是描述性的;此外,感染的毒株、时间和序列往往未知。相比之下,在小鼠中,感染条件明确,大量实验参数可以随意改变。因此,小鼠模型为基于流行病学观察的假设提供了实验检验的机会。特别是,可以建立功能获得或功能丧失模型,以评估免疫系统的不同组成部分(单独或组合)在二次感染或接种疫苗后如何促进保护或发病机制。此外,小鼠模型已用于抗病毒药物的临床前测试或疫苗开发研究。由于动物模型的固有局限性,基于小鼠实验得出的结论必须谨慎地外推至人类的DENV感染。然而,小鼠模型研究是体外和流行病学数据的有益补充,可能会勾勒出未来人体研究中值得关注的新领域。

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