Choo Q L, Kuo G, Ralston R, Weiner A, Chien D, Van Nest G, Han J, Berger K, Thudium K, Kuo C
Chiron Corporation, Emeryville, CA 94608.
Proc Natl Acad Sci U S A. 1994 Feb 15;91(4):1294-8. doi: 10.1073/pnas.91.4.1294.
A high incidence of community-acquired hepatitis C virus infection that can lead to the progressive development of chronic active hepatitis, liver cirrhosis, and primary hepatocellular carcinoma occurs throughout the world. A vaccine to control the spread of this agent that represents a major cause of chronic liver disease is therefore needed. Seven chimpanzees (Pan troglodytes) have been immunized with both putative envelope glycoproteins [E1 (gp33) and E2 (gp72)] that were copurified from HeLa cells infected with a recombinant vaccinia virus expression vector. Despite the induction of a weak humoral immune response to these viral glycoproteins in experimentally infected chimpanzees, a strong humoral immune response was obtained in all vaccines. The five highest responders showed complete protection against an i.v. challenge with homologous hepatitis C virus 1. The remaining two vaccines became infected, but both infection and disease may have been ameliorated in comparison with four similarly challenged control chimpanzees, all of which developed acute hepatitis and chronic infections. These results provide considerable encouragement for the eventual control of hepatitis C virus infection by vaccination.
社区获得性丙型肝炎病毒感染的高发病率在全球范围内都有发生,这种感染可导致慢性活动性肝炎、肝硬化和原发性肝细胞癌的逐步发展。因此,需要一种疫苗来控制这种作为慢性肝病主要病因的病原体的传播。七只黑猩猩(黑猩猩)用从感染重组痘苗病毒表达载体的HeLa细胞中共同纯化的两种假定包膜糖蛋白[E1(gp33)和E2(gp72)]进行了免疫接种。尽管在实验感染的黑猩猩中对这些病毒糖蛋白诱导了微弱的体液免疫反应,但在所有疫苗接种动物中都获得了强烈的体液免疫反应。五只反应最强的动物对静脉注射同源丙型肝炎病毒1的攻击表现出完全的保护作用。其余两只接种疫苗的动物被感染,但与四只同样受到攻击的对照黑猩猩相比,感染和疾病可能都有所减轻,所有对照黑猩猩都发展为急性肝炎和慢性感染。这些结果为最终通过接种疫苗控制丙型肝炎病毒感染提供了相当大的鼓舞。