Elahi S M, Shen S H, Harpin S, Talbot B G, Elazhary Y
Virology Section, Faculty of Veterinary Medicine, University of Montreal, Saint-Hyacinthe, Quebec, Canada.
Arch Virol. 1999;144(6):1057-70. doi: 10.1007/s007050050569.
Two replication-defective human adenovirus recombinants encoding the NS3 protein (p80) of bovine viral diarrhea virus (BVDV) under the control of a modified adenovirus major later promoter (BM5), rAdBM5/NS3, and human cytomegalovirus promoter (CMV5), rAdCMV5/NS3, were constructed. These two recombinant adenoviruses were tested for their expression of the NS3 protein in vitro in three different cell lines and also in vivo for the induction of BVDV-specific immune responses in mice. The recombinant adenoviruses containing two different promoters induced different levels of humoral responses to the NS3 protein. The rAdBM5/NS3 was used to vaccinate mice in order to evaluate the ability of the NS3 protein in the induction of cellular immune responses. The rAdBM5/NS3 did not cause a stimulation of cell proliferation but caused a very strong increase in production of IFN-gamma in murine mononuclear cells stimulated in vivo by BVDV strains of genotype 1 and 2.
构建了两种复制缺陷型人腺病毒重组体,分别是在改良腺病毒主要晚期启动子(BM5)控制下编码牛病毒性腹泻病毒(BVDV)NS3蛋白(p80)的rAdBM5/NS3,以及在人巨细胞病毒启动子(CMV5)控制下的rAdCMV5/NS3。对这两种重组腺病毒在三种不同细胞系中进行了NS3蛋白表达的体外测试,并在小鼠体内测试了其诱导BVDV特异性免疫反应的能力。含有两种不同启动子的重组腺病毒诱导了对NS3蛋白不同水平的体液反应。使用rAdBM5/NS3对小鼠进行免疫接种,以评估NS3蛋白诱导细胞免疫反应的能力。rAdBM5/NS3未引起细胞增殖刺激,但在体内受1型和2型BVDV毒株刺激的小鼠单核细胞中,导致IFN-γ产生大幅增加。