Tsukiyama K, Yoshikawa Y, Kamata H, Imaoka K, Asano K, Funahashi S, Maruyama T, Shida H, Sugimoto M, Yamanouchi K
Institute of Medical Science, University of Tokyo, Japan.
Arch Virol. 1989;107(3-4):225-35. doi: 10.1007/BF01317919.
Recombinant vaccinia virus (RVV) containing the full-length cDNA of rinderpest virus (RV)-haemagglutinin (H) gene was constructed. The H gene was inserted into the attenuated vaccine strain of vaccinia virus (VV), Le 16 m0, with two different promoters, namely cowpox virus A-type inclusion body (ATI) promoter or VV 7.5 kilodalton (P7.5) promoter. These RVVs produced the same sized fully glycosylated RV-H protein in RK 13 cells as that of the authentic RV-H. Their heat stability in the lyophylized state was similar to that of the parental VV. All rabbits immunized with these RVVs produced virus neutralizing (VN) antibody to RV as well as anti RV-H antibody. Four weeks after immunization, these animals were challenged with RV intravenously. None of the RVV-immunized rabbits developed any clinical signs of RV infection except one which was immunized with RVV containing the ATI promoter and developed low VN titer. These results indicate the possibility of developing a heat-stable recombinant vaccine for the eradication of rinderpest in tropical countries without cold storage systems.
构建了含有牛瘟病毒(RV)血凝素(H)基因全长cDNA的重组痘苗病毒(RVV)。将H基因插入痘苗病毒(VV)的减毒疫苗株Le 16 m0中,带有两种不同的启动子,即牛痘病毒A型包涵体(ATI)启动子或VV 7.5千道尔顿(P7.5)启动子。这些RVV在RK 13细胞中产生的完全糖基化的RV-H蛋白大小与天然RV-H相同。它们在冻干状态下的热稳定性与亲本VV相似。所有用这些RVV免疫的兔子都产生了针对RV的病毒中和(VN)抗体以及抗RV-H抗体。免疫四周后,这些动物静脉内接种RV进行攻毒。除了一只用含有ATI启动子的RVV免疫且VN效价较低的兔子外,没有一只RVV免疫的兔子出现任何RV感染的临床症状。这些结果表明,在没有冷藏系统的热带国家,有可能开发出一种热稳定的重组疫苗来根除牛瘟。