Tyler G V, Snyder R L, Summers J
Lab Invest. 1986 Jul;55(1):51-5.
Six woodchucks, 10 1/2 months of age, injected intramuscularly with 0.02 ml of woodchuck hepatitis virus (WHV)-positive serum and two woodchucks of similar age and origin injected with phosphate buffered saline were studied by serial blood samples and liver biopsy sections over an 18 week period. Serum samples were assayed for WHV surface antigen (WHsAg), its corresponding antibody (anti-WHs) and antibody to WHV core antigen (anti-WHc). WHV core antigen (WHcAg) was detected in liver biopsy sections by fluorescent labeled anti-WHc, and WHsAg was detected by the Victoria blue stain. All six experimentally infected woodchucks eventually developed anti-WHs and four developed serologic and histologic signs of acute hepatitis. Hepatic lesions resembled lesions described in the livers of chimpanzees and humans with acute hepatitis B viral infections. The first histologic signs of liver change coincided with the appearance of WHsAg within the serum and WHcAg within the cytoplasm of hepatocytes. After WHcAg was no longer detected in the serum, WHsAg appeared in the cytoplasm of hepatocytes. Microfocal areas of hepatic necrosis were associated with aggregates of lymphocytes, macrophages, and a few neutrophils and plasma cells. The periportal exudate became increasingly abundant during the 18-week study period in the four animals with acute hepatitis. The results from this study indicate that acute hepatitis may be induced in the woodchuck by experimental infection with WHV. Furthermore, the woodchuck might serve as an excellent model for the study of the pathogenesis of acute viral hepatitis in man.
对6只10个半月大的土拨鼠进行研究,给它们肌肉注射0.02毫升土拨鼠肝炎病毒(WHV)阳性血清,同时给2只年龄和来源相似的土拨鼠注射磷酸盐缓冲盐水,在18周的时间里通过连续采集血样和肝活检切片进行研究。检测血清样本中的WHV表面抗原(WHsAg)、其相应抗体(抗-WHs)以及抗WHV核心抗原抗体(抗-WHc)。通过荧光标记的抗-WHc在肝活检切片中检测WHV核心抗原(WHcAg),通过维多利亚蓝染色检测WHsAg。所有6只实验感染的土拨鼠最终都产生了抗-WHs,4只出现了急性肝炎的血清学和组织学特征。肝脏病变类似于感染急性乙型肝炎病毒的黑猩猩和人类肝脏中所描述的病变。肝脏变化的首个组织学特征与血清中WHsAg的出现以及肝细胞胞质中WHcAg的出现同时发生。在血清中不再检测到WHcAg后,WHsAg出现在肝细胞胞质中。肝坏死的微灶区域与淋巴细胞、巨噬细胞以及少量中性粒细胞和浆细胞的聚集有关。在为期18周的研究期间,4只患有急性肝炎的动物的门周渗出物变得越来越多。该研究结果表明,通过实验感染WHV可在土拨鼠中诱发急性肝炎。此外,土拨鼠可能是研究人类急性病毒性肝炎发病机制的极佳模型。