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非人类灵长类动物的 Epstein-Barr 病毒感染模型。

Nonhuman primate models for Epstein-Barr virus infection.

机构信息

Department of Medicine, Brigham & Women's Hospital, Harvard Medical School, MCP 836, 181 Longwood Avenue, Boston, MA 02115, United States.

出版信息

Curr Opin Virol. 2013 Jun;3(3):233-7. doi: 10.1016/j.coviro.2013.03.003. Epub 2013 Apr 3.

Abstract

Epstein-Barr virus (EBV) is a human herpesvirus that infects nearly all humans by adulthood and is associated with a spectrum of human diseases including Infectious Mononucleosis, Hodgkin Lymphoma, Nasopharyngeal Carcinoma, and lymphomas in immunosuppressed hosts. Nonhuman primate (NHP) animal models provide important experimental systems for studying EBV infection. There has been significant progress in studies of EBV-related herpesviruses, or lymphocryptoviruses (LCV), that naturally infect New and Old World NHPs. Prototypes for New and Old World LCV have been cloned and sequenced, humoral and cellular immune responses to LCV in NHP have been characterized, experimental LCV infections in naïve rhesus macaques have been successful, and a genetic system to manipulate specific viral genes in rhesus LCV (rhLCV) has been developed. These advances have led to new insights in the dynamic interactions with the host during acute and persistent EBV infection and can provide a novel platform for EBV vaccine development. Further development and utilization of the rhLCV animal model would be greatly enhanced by expansion of LCV-free breeding colonies as a reliable source of naïve animals for experimental studies. NHP animal models for EBV infection provide unique opportunities for understanding the biology of EBV infection in humans and translating that knowledge into effective vaccines against EBV-induced diseases.

摘要

EB 病毒(EBV)是一种人类疱疹病毒,几乎在成年前就感染了所有人类,并与一系列人类疾病相关,包括传染性单核细胞增多症、霍奇金淋巴瘤、鼻咽癌和免疫抑制宿主中的淋巴瘤。非人类灵长类动物(NHP)动物模型为研究 EBV 感染提供了重要的实验系统。对自然感染新旧世界 NHP 的 EBV 相关疱疹病毒或淋巴隐病毒(LCV)的研究取得了重大进展。已成功克隆和测序了新旧世界 LCV 的原型,对 NHP 中 LCV 的体液和细胞免疫反应进行了表征,对天真恒河猴进行了实验性 LCV 感染,并且开发了一种用于操纵恒河猴 LCV(rhLCV)中特定病毒基因的遗传系统。这些进展导致了在急性和持续性 EBV 感染期间与宿主的动态相互作用的新见解,并为 EBV 疫苗开发提供了新的平台。通过扩大无 LCV 繁殖群体作为实验研究的天真动物的可靠来源,rhLCV 动物模型的进一步开发和利用将得到极大增强。EBV 感染的 NHP 动物模型为了解 EBV 感染在人类中的生物学特性并将该知识转化为针对 EBV 诱导疾病的有效疫苗提供了独特的机会。

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