Kato K
Institute for Molecular and Cellular Biology, Osaka University.
Nihon Rinsho. 1993 Feb;51(2):525-30.
Hepatitis B virus (HBV) surface antigen (HBsAg) genes were injected directly into liver of adult rodents by HVJ-liposome method in order to develop HBV model rodents. From immunohistochemical analysis, liver cells transfected with the HBsAg genes expressed the Ag in vivo. Transfection of plasmid expressing only small S antigen (secretory type) resulted in detection of HBsAg in sera of rats for 9 days. On successive injection of the HBsAg (large S, middle S, and small S) genes, the antibody to HBsAg was produced in the sera of rats. Furthermore, liver tissues in the rats showed infiltration of lymphocytes and hepatocytes degeneration in the parenchyma and inflammation of Glisson's sheaths histologically. The HVJ-liposome method may be suitable for evaluating a series of process from expression of viral components to induction of viral diseases in the living body.
为了建立乙型肝炎病毒(HBV)模型啮齿动物,采用HVJ-脂质体法将HBV表面抗原(HBsAg)基因直接注入成年啮齿动物的肝脏。通过免疫组织化学分析,转染了HBsAg基因的肝细胞在体内表达了该抗原。转染仅表达小S抗原(分泌型)的质粒后,在大鼠血清中检测到HBsAg达9天。连续注射HBsAg(大S、中S和小S)基因后,大鼠血清中产生了抗HBsAg抗体。此外,组织学检查显示大鼠肝脏组织有淋巴细胞浸润、实质内肝细胞变性以及Glisson鞘炎症。HVJ-脂质体法可能适用于评估从病毒成分表达到活体中病毒疾病诱导的一系列过程。