Center for the Study of Hepatitis C, The Rockefeller University, New York, New York 10065, USA.
J Clin Invest. 2010 Mar;120(3):650-3. doi: 10.1172/JCI42338. Epub 2010 Feb 22.
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.
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。