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用于乙型肝炎病毒研究的体内模型系统

In Vivo Model Systems for Hepatitis B Virus Research.

作者信息

Ortega-Prieto Ana Maria, Cherry Catherine, Gunn Harry, Dorner Marcus

机构信息

Section of Virology, Department of Medicine , Imperial College London , W2 1PG London , U.K.

出版信息

ACS Infect Dis. 2019 May 10;5(5):688-702. doi: 10.1021/acsinfecdis.8b00223. Epub 2019 Jan 8.

Abstract

Hepatitis B virus (HBV) affects more than 257 million people globally, resulting in progressively worsening liver disease, manifesting as fibrosis, cirrhosis, and hepatocellular carcinoma. The exceptionally narrow species tropism of HBV restricts its natural hosts to humans and non-human primates, including chimpanzees, gorillas, gibbons, and orangutans. The unavailability of completely immunocompetent small-animal models has contributed to the lack of curative therapeutic interventions. Even though surrogates allow the study of closely related viruses, their host genetic backgrounds, immune responses, and molecular virology differ from those of HBV. Various different models, based on either pure murine or xenotransplantation systems, have been introduced over the past years, often making the choice of the optimal model for any given question challenging. Here, we offer a concise review of in vivo model systems employed to study HBV infection and steps in the HBV life cycle or pathogenesis.

摘要

全球有超过2.57亿人感染乙型肝炎病毒(HBV),导致肝脏疾病逐渐恶化,表现为纤维化、肝硬化和肝细胞癌。HBV异常狭窄的宿主嗜性将其天然宿主限制为人类和非人类灵长类动物,包括黑猩猩、大猩猩、长臂猿和猩猩。完全具有免疫活性的小动物模型的缺乏导致了治愈性治疗干预措施的缺失。尽管替代模型可用于研究密切相关的病毒,但其宿主遗传背景、免疫反应和分子病毒学与HBV不同。在过去几年中,人们引入了各种基于纯小鼠或异种移植系统的不同模型,这常常使得为任何特定问题选择最佳模型具有挑战性。在这里,我们简要综述了用于研究HBV感染以及HBV生命周期或发病机制步骤的体内模型系统。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/518f/6515358/37dd3925a50e/id-2018-00223v_0001.jpg

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