Skelly J, Howard C R, Zuckerman A J
Nature. 1981 Mar 5;290(5801):51-4. doi: 10.1038/290051a0.
The immunoprophylaxis of hepatitis B is hampered by the lack of a technique for growing hepatitis B virus (HBV) in tissue culture. Plasma from persistently infected individuals, one source of viral antigen, contains characteristic 22-nm spherical particles which share a common antigen (the hepatitis B surface antigen or HBsAg) with the outer envelope of the 42-nm double-shelled DNA virus. Highly purified inactivated 22-nm particles have been shown to be safe and to confer protective immunity against HBV in a recent large-scale clinical trial. We have already described the extraction from the particles of a complex of two proteins which are antigenic determinants of HBV--the polypeptide with molecular weight (MW) between 22,000 and 24,000 (called p23) and the glycosylated polypeptide (called gp28) with MW in the range 26,000--29,000 which is thought to be the glycosylated form of p23. We now report the preparation from this complex of water-soluble protein micelles which may be a suitable basis for a second-generation hepatitis B vaccine.
由于缺乏在组织培养中培养乙型肝炎病毒(HBV)的技术,乙型肝炎的免疫预防受到了阻碍。持续感染个体的血浆是病毒抗原的一个来源,其中含有特征性的22纳米球形颗粒,这些颗粒与42纳米双壳DNA病毒的外膜具有共同抗原(乙型肝炎表面抗原或HBsAg)。在最近的一项大规模临床试验中,高度纯化的灭活22纳米颗粒已被证明是安全的,并能赋予针对HBV的保护性免疫。我们已经描述了从颗粒中提取两种蛋白质的复合物,这两种蛋白质是HBV的抗原决定簇——分子量(MW)在22000至24000之间的多肽(称为p23)和MW在26000 - 29000范围内的糖基化多肽(称为gp28),后者被认为是p23的糖基化形式。我们现在报告从这种复合物制备水溶性蛋白质微团,这可能是第二代乙型肝炎疫苗的合适基础。