Vidor E, Dumas R, Porteret V, Bailleux F, Veitch K
Aventis Pasteur, Medical Department, Clinical Development, 57 Avenue Leclerc, 69007 Lyon, France.
Eur J Clin Microbiol Infect Dis. 2004 Apr;23(4):300-9. doi: 10.1007/s10096-003-1094-0. Epub 2004 Mar 6.
Inactivated hepatitis A vaccines were developed in the 1980s and were introduced during the early 1990s. The Aventis Pasteur (AvP) inactivated hepatitis A virus antigen is used in several different vaccine formulations licensed for adults and children. Presented here are the immunogenicity results compiled from 37 clinical trials performed in 20 different countries between 1991 and 2001 in which these vaccines were administered to adults (16 years of age and over), children (aged 12 months-17 years), and infants (younger than 12 months). The accumulated clinical experience with these hepatitis A virus-containing vaccines demonstrates the excellent immunogenicity of this antigen in a wide range of situations. As with other licensed inactivated hepatitis A vaccines, immunological priming is achieved in virtually all vaccinees after a single-dose primary immunization, and it may be reinforced by a booster vaccination administered 6-36 months after the primary vaccination.
灭活甲肝疫苗于20世纪80年代研发,并于20世纪90年代初投入使用。赛诺菲巴斯德(AvP)公司的灭活甲肝病毒抗原被用于多种不同的疫苗配方,这些配方已获得成人和儿童疫苗许可。本文展示的是1991年至2001年间在20个不同国家进行的37项临床试验的免疫原性结果,这些试验中,上述疫苗被用于成人(16岁及以上)、儿童(12个月至17岁)和婴儿(12个月以下)。这些含甲肝病毒疫苗的累积临床经验表明,该抗原在广泛的情况下具有出色的免疫原性。与其他已获许可的灭活甲肝疫苗一样,几乎所有接种者在单剂量初次免疫后都能实现免疫启动,并且在初次接种后6至36个月进行的加强接种可能会增强免疫效果。