HBV感染的动物模型研究进展

杨炜峰; 苗振川; 宋希军; 尹明

doi:10.3969/j.issn.1001-5256.2021.05.002

HBV感染的动物模型研究进展

DOI: 10.3969/j.issn.1001-5256.2021.05.002

北京维通达生物技术有限公司，北京 100012

利益冲突声明：所有作者均声明不存在利益冲突。

作者贡献声明：杨炜峰、苗振川、宋希军负责调研整理文献，设计论文框架，起草论文，整理数据和修订论文；尹明负责终审论文。

详细信息

作者简介:
杨炜峰(1977—)，博士，主要从事大鼠、小鼠模型的研发工作

通信作者:
尹明，yinming@vital-bj.com

中图分类号: R512.62
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出版历程
- 收稿日期: 2021-02-26
- 录用日期: 2021-02-26
- 出版日期: 2021-05-20

Research advances in animal models of hepatitis B virus infection

Beijing Vitalstar Biotechnology Co. Ltd., Beijing 100012, China

摘要

摘要: 理想的HBV临床前动物模型，其肝细胞应包括允许HBV进入、cccDNA形成和与之相互作用的先天性及获得性免疫系统。由于HBV严格的种属特异性，自然只感染人类和黑猩猩，至今还没有建立一个有效的模型，能够真实地再现HBV感染的免疫和发病机制。综述了目前常用的五种小鼠模型：HBV转基因模型、高压水动力注射模型、AAV-HBV转染模型、cccDNA替代模型和人鼠嵌合肝脏模型。展望了未来可能出现的模型，比如hNTCP转基因的食蟹猴、恒河猴和猪等模型等。以期为研究人员选择这些模型提供参照，加快药筛进程、验证新疗法和更好解决HBV生物学发病机制等方面的问题。
- 乙型肝炎病毒 /
- 疾病模型, 动物 /
- 小鼠
Abstract: For the ideal preclinical animal model of hepatitis B virus (HBV), its hepatocytes should allow HBV entry and cccDNA generation and have both innate and adaptive immune systems. However, HBV only naturally infects humans and chimpanzees due to highly restricted species specificity, and no effective model has been established so far to truly reflect the immune mechanism and pathogenesis of HBV infection. This article reviews five commonly used mouse models, i.e., HBV transgenic model, HBV plasmid DNA hydrodynamic injection model, AAV-HBV transfection model, cccDNA surrogate model, and human-mouse chimeric liver model, and looks forward to the new models that will appear in the future, such as hNTCP transgenic cynomolgus monkey, rhesus monkey, or pig models, so as to provide a reference for researchers to select these models, accelerate the process of drug screening, validate new therapies, and better solve the problems of HBV biological pathogenesis.
- Hepatitis B Virus /
- Disease Models, Animal /
- Mice

HTML全文

表 1 HBV感染的小鼠模型特征

特征	HBV转基因小鼠模型	HDI小鼠模型¹⁾	AAV-HBV转染小鼠模型	cccDNA替代小鼠模型	人鼠肝脏嵌合小鼠模型	人免疫系统和肝双人源化小鼠模型
病毒或载体类型	整合HBV基因	裸HBV基因	AAV- HBV基因	重组cccDNA	HBV病毒	HBV病毒
病毒进入	-	-	-	-	+	+
模型感染性	-	-	-	-	+	+
复制过程	+	短暂的	+	+	+	+
cccDNA	-	-	?/-	+	+	+
病毒持久性	+	短暂的	剂量和品系依赖	+	+	+
免疫系统	+	+	+/-	+	-	人的免疫系统
丹氏颗粒分泌	+	+	+	+	+	+
治愈可能性	-	-	+	+	+	+
感染类型	慢性	急性	急性/慢性	慢性	慢性	慢性
肝细胞背景	鼠	鼠	鼠	鼠	人和鼠	人和鼠
制备难易度	容易	容易	容易	容易	中等	困难
注：1)高压水动力注射小鼠模型；AAV，腺相关病毒; “+”表示有或包含；“-”表示无或没有；“+/-”表示有或无均存在；“?/-”表示有争议或没有。

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表 2 人鼠嵌合肝脏小鼠(人源化肝脏模型)模型

特征	uPA-SCID	FRG	TK-NOG	AFC8	URG^Ⓡ
肝细胞毒性基因	uPA	Fah敲除	疱疹病毒胸苷激酶	FK508-Caspase8	uPA
肝损伤诱导	不能	可以；NTBC	可以；gancyclovir	可以；AP20187	可以；Dox
扩繁效率	低	100%	50%;纯合雄性不育	-	100%
肝细胞移植时间	离乳前	任何时间	成年	成年	任何时间
转基因损伤恢复	可能	不会	-	-	可能
高的人肝嵌合比例(＞90%)	可以	可以	可以	不能	可以
长期研究的可能性	可以	可以	可以	-	可以
肝癌发生率	未发现	很少; 高重建鼠未发现	未发现	未发现	未发现
注：“-”表示文献中没有报道相关数据。

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