Feitelson M A, DeTolla L J, Zhou X D
Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111.
J Virol. 1988 Apr;62(4):1408-15. doi: 10.1128/JVI.62.4.1408-1415.1988.
BALB/c nude mice were injected intrahepatically with hepatitis B virus (HBV) DNA prepared from recombinant plasmids. Hepatitis B surface antigen appeared in the circulation in 19 of 23 mice (82%) 3 to 20 weeks postinjection and persisted for more than 6 months in most animals. Hepatitis B e antigen appeared transiently in the circulation in 12 of the 23 mice (52%) within a few weeks after the appearance of hepatitis B surface antigen. Antibodies to the core, X, and/or polymerase gene products of HBV have also been observed in 14 (61%) of the mice. Histopathological examination of the livers at 7 months postinjection demonstrated that nearly half had characteristics consistent with chronic hepatitis. HBV DNA appeared to be integrated into host liver DNA. No evidence of viral replication was observed in sera or livers from these mice at 7 months postinjection. These results demonstrate that an HBV chronic carrierlike state can be established in mice and that such a model could be used to study host and virus factors important in the establishment and maintenance of HBV-associated chronic liver disease.
将重组质粒制备的乙型肝炎病毒(HBV)DNA经肝内注射给BALB/c裸鼠。在注射后3至20周,23只小鼠中有19只(82%)的循环系统中出现了乙型肝炎表面抗原,且在大多数动物中持续存在超过6个月。在乙型肝炎表面抗原出现后的几周内,23只小鼠中有12只(52%)的循环系统中短暂出现了乙型肝炎e抗原。在14只(61%)小鼠中还观察到了针对HBV核心、X和/或聚合酶基因产物的抗体。注射后7个月对肝脏进行组织病理学检查显示,近一半具有与慢性肝炎相符的特征。HBV DNA似乎整合到了宿主肝脏DNA中。在注射后7个月,这些小鼠的血清或肝脏中未观察到病毒复制的证据。这些结果表明,可在小鼠中建立类似HBV慢性携带者的状态,且这样的模型可用于研究在HBV相关慢性肝病的发生和维持中起重要作用的宿主和病毒因素。