Sharma M D, Maillard P, Vrati S, Mukherjee R, Rajagopalan M S, Poynard T, Talwar G P, Pillot J
National Institute of Immunology, New Delhi, India.
J Med Virol. 1990 Jan;30(1):36-41. doi: 10.1002/jmv.1890300108.
An experimental model of sporadic non-A non-B hepatitis involving a Fab nonimmune binding activity in stools was established in the rhesus monkey. The first animal was inoculated intravenously with a stool extract from a French patient who had never left the country and in whom post-transfusion hepatitis was excluded. Four passages were performed, and the infection was transmitted by parenteral as well as the oral routes by inoculation of stools or liver extracts. Infection led in three monkeys to reversible hepatocyte injury manifested by a transitory increase in serum aminotransferases. The other three animals, in which persistently high levels of aminotransferases was observed, were sacrificed on day 60 after inoculation. The incubation period, as evidenced by elevation of aminotransferases was about 3 to 4 weeks. The infectious agent was transitorily present in the stools before aminotransferase elevation. The presence of the infectious agent in the stools was correlated with the nonimmune Fab binding activity.
在恒河猴中建立了一种涉及粪便中Fab非免疫结合活性的散发性非甲非乙型肝炎实验模型。第一只动物静脉注射了一名从未离开过该国且已排除输血后肝炎的法国患者的粪便提取物。进行了四代传代,通过接种粪便或肝脏提取物经胃肠外和口服途径传播感染。三只猴子出现感染,表现为血清转氨酶短暂升高,导致可逆性肝细胞损伤。另外三只动物在接种后第60天被处死,其血清转氨酶水平持续居高不下。转氨酶升高表明潜伏期约为3至4周。在转氨酶升高之前,粪便中短暂存在感染因子。粪便中感染因子的存在与非免疫Fab结合活性相关。