McCabe Victoria J, Spibey Norman
Department of Molecular Studies, Intervet UK Ltd., Walton Manor, Walton, Milton Keynes, BUCKS, MK7 7AJ, UK.
Vaccine. 2005 Nov 16;23(46-47):5380-8. doi: 10.1016/j.vaccine.2005.05.038. Epub 2005 Jul 5.
It has previously been demonstrated that recombinant myxoma viruses expressing FCV capsid protein are capable of eliciting protective responses against virulent FCV challenge, following vaccination, in cats. An attempt was made to produce a bivalent myxoma recombinant expressing the capsid protein genes of both FCV strains F9 and LS015. The FCV capsid protein genes were inserted into the myxoma growth factor gene (MGF) locus, and the serine protease inhibitor (SERP 2) gene locus. Subsequent recombination between myxoma-FCV viruses resulted in a recombinant expressing a chimeric form of the capsid protein. Nonetheless, cats immunised with this myxoma-FCV recombinant demonstrate high levels of serum neutralising antibodies against both F9 and LS015 strains. Such a chimeric vaccine may provide effective protection against a wide range of FCV strains.
先前已经证明,表达猫杯状病毒(FCV)衣壳蛋白的重组黏液瘤病毒在接种疫苗后能够引发针对强毒FCV攻击的保护性反应,在猫身上。曾尝试制备一种表达FCV F9和LS015两个毒株衣壳蛋白基因的二价黏液瘤重组体。将FCV衣壳蛋白基因插入黏液瘤生长因子基因(MGF)位点和丝氨酸蛋白酶抑制剂(SERP 2)基因位点。随后黏液瘤-FCV病毒之间的重组产生了一种表达衣壳蛋白嵌合形式的重组体。尽管如此,用这种黏液瘤-FCV重组体免疫的猫表现出针对F9和LS015毒株的高水平血清中和抗体。这样一种嵌合疫苗可能对多种FCV毒株提供有效的保护。