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本文引用的文献

1
Human liver chimeric mice provide a model for hepatitis B and C virus infection and treatment.人源化肝脏嵌合小鼠为乙型和丙型肝炎病毒感染和治疗提供了模型。
J Clin Invest. 2010 Mar;120(3):924-30. doi: 10.1172/JCI40094. Epub 2010 Feb 22.
2
Persistent hepatitis C virus infection in microscale primary human hepatocyte cultures.微尺度原代人肝细胞培养物中持续性丙型肝炎病毒感染。
Proc Natl Acad Sci U S A. 2010 Feb 16;107(7):3141-5. doi: 10.1073/pnas.0915130107. Epub 2010 Feb 1.
3
Highly efficient generation of human hepatocyte-like cells from induced pluripotent stem cells.高效诱导多能干细胞生成人肝细胞样细胞。
Hepatology. 2010 Jan;51(1):297-305. doi: 10.1002/hep.23354.
4
Generation of functional human hepatic endoderm from human induced pluripotent stem cells.从人诱导多能干细胞生成功能性人肝内胚层。
Hepatology. 2010 Jan;51(1):329-35. doi: 10.1002/hep.23335.
5
Towards a small animal model for hepatitis C.建立丙型肝炎小动物模型。
EMBO Rep. 2009 Nov;10(11):1220-7. doi: 10.1038/embor.2009.223. Epub 2009 Oct 16.
6
A mouse model of inducible liver injury caused by tet-on regulated urokinase for studies of hepatocyte transplantation.四环素调控的尿激酶诱导的肝损伤小鼠模型用于肝细胞移植研究。
Am J Pathol. 2009 Nov;175(5):1975-83. doi: 10.2353/ajpath.2009.090349. Epub 2009 Oct 1.
7
Visualizing hepatitis C virus infections in human liver by two-photon microscopy.通过双光子显微镜观察人类肝脏中的丙型肝炎病毒感染情况。
Gastroenterology. 2009 Oct;137(4):1448-58. doi: 10.1053/j.gastro.2009.07.050. Epub 2009 Jul 24.
8
Preerythrocytic, live-attenuated Plasmodium falciparum vaccine candidates by design.设计的恶性疟原虫前体红细胞期减毒活疫苗候选物。
Proc Natl Acad Sci U S A. 2009 Aug 4;106(31):13004-9. doi: 10.1073/pnas.0906387106. Epub 2009 Jul 22.
9
Humanized mice for modeling human infectious disease: challenges, progress, and outlook.用于人类传染病建模的人源化小鼠:挑战、进展与展望。
Cell Host Microbe. 2009 Jul 23;6(1):5-9. doi: 10.1016/j.chom.2009.06.006.
10
In vitro differentiation of embryonic and adult stem cells into hepatocytes: state of the art.胚胎干细胞和成体干细胞向肝细胞的体外分化:现状
Stem Cells. 2009 Mar;27(3):577-605. doi: 10.1634/stemcells.2008-0963.

研究人类嗜肝性感染的新视野。

New horizons for studying human hepatotropic infections.

机构信息

Center for the Study of Hepatitis C, The Rockefeller University, New York, New York 10065, USA.

出版信息

J Clin Invest. 2010 Mar;120(3):650-3. doi: 10.1172/JCI42338. Epub 2010 Feb 22.

DOI:10.1172/JCI42338
PMID:20179350
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2827969/
Abstract

The liver serves as a target organ for several important pathogens, including hepatitis B and C viruses (HBV and HCV, respectively) and the human malaria parasites, all of which represent serious global health problems. Because these pathogens are restricted to human hepatocytes, research in small animals has been compromised by the frailty of the current mouse xenotransplantation models. In this issue of the JCI, Bissig et al. demonstrate robust HBV and HCV infection in a novel xenotransplantation model in which large numbers of immunodeficient mice with liver injury were engrafted with significant quantities of human hepatocytes. This technical advance paves the way for more widespread use of human liver chimeric mice and forms the basis for creating increasingly complex humanized mouse models that could prove useful for studying immunopathogenesis and vaccine development against hepatotropic pathogens.

摘要

肝脏是几种重要病原体的靶器官,包括乙型肝炎和丙型肝炎病毒(HBV 和 HCV)以及人类疟原虫,这些都是严重的全球健康问题。由于这些病原体仅限于人类肝细胞,因此当前的小鼠异种移植模型的脆弱性限制了小动物研究。在本期 JCI 中,Bissig 等人证明了新型异种移植模型中 HBV 和 HCV 的感染非常稳定,该模型中大量肝损伤的免疫缺陷小鼠被大量人源肝细胞移植。这一技术进步为更广泛地使用人肝嵌合小鼠铺平了道路,并为创建越来越复杂的人源化小鼠模型奠定了基础,这些模型可能有助于研究针对嗜肝病原体的免疫发病机制和疫苗开发。