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动物模型在巨细胞病毒感染新疗法研发中的关键作用。

Pivotal role of animal models in the development of new therapies for cytomegalovirus infections.

作者信息

Kern Earl R

机构信息

The University of Alabama at Birmingham, Department of Pediatrics, CHB 128, 1600 6th Avenue South, Birmingham, AL 35233, United States.

出版信息

Antiviral Res. 2006 Sep;71(2-3):164-71. doi: 10.1016/j.antiviral.2006.05.018. Epub 2006 Jun 19.

Abstract

Since human cytomegalovirus (CMV) is extremely species specific and does not replicate in experimental animal tissues, animal models for the evaluation of antiviral agents for these infections have utilized surrogate animal viruses including murine CMV, rat CMV and guinea pig CMV. Murine CMV and rat CMV infections in normal and immunocompromised animals provide models of disseminated infection and are ideal for screening of new agents. While guinea pig CMV infection in immunocompromised animals also provides a model for disseminated disease, the model for congenital CMV is unique among all the experimental models. While these models have played a major role in the development of ganciclovir, foscarnet and cidofovir, they do not provide information directly related to human CMV, nor are they useful for evaluation of agents that are active only against human CMV. The SCID-hu mouse models in which human tissue is infected with human CMV has been very useful in the development of new antiviral agents such as maribavir and cyclopropavir. Collectively these experimental CMV infections provide a variety of models representing various aspects of CMV infection in humans that are highly predictive for antiviral efficacy in humans.

摘要

由于人类巨细胞病毒(CMV)具有极强的种属特异性,且不在实验动物组织中复制,因此用于评估针对这些感染的抗病毒药物的动物模型采用了替代动物病毒,包括鼠巨细胞病毒、大鼠巨细胞病毒和豚鼠巨细胞病毒。正常和免疫受损动物中的鼠巨细胞病毒和大鼠巨细胞病毒感染提供了播散性感染模型,是筛选新药物的理想模型。虽然免疫受损动物中的豚鼠巨细胞病毒感染也提供了播散性疾病模型,但先天性CMV模型在所有实验模型中是独特的。虽然这些模型在更昔洛韦、膦甲酸钠和西多福韦的研发中发挥了重要作用,但它们并未提供与人类CMV直接相关的信息,也不适用于评估仅对人类CMV有活性的药物。用人CMV感染人体组织的SCID-hu小鼠模型在开发诸如马立巴韦和环丙沙星等新型抗病毒药物方面非常有用。总体而言,这些实验性CMV感染提供了多种模型,代表了人类CMV感染的各个方面,对人类抗病毒疗效具有高度预测性。

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