Hu L, Ngichabe C, Trimarchi C V, Esposito J J, Scott F W
Cornell Feline Health Center, Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.
Vaccine. 1997 Aug-Sep;15(12-13):1466-72. doi: 10.1016/s0264-410x(97)00062-5.
A raccoon poxvirus (RCNV) recombinant for immunizing against feline panleukopenia and rabies was developed by homologous recombination with a chimeric plasmid for insertional inactivation of the RCNV thymidine kinase gene. The recombinant, RCN-FPV/VP2-rabG, coexpressed the feline panleukopenia virus (FPV) VP2 protein and the rabies virus spike glycoprotein (rabG) under oppositely oriented vaccinia virus P11 promoters. Cats vaccinated subcutaneously with the recombinant showed relatively high neutralizing antibody responses against rabies virus and FPV, and protection against an otherwise virulent FPV challenge with no drop in white blood cell count. Because of containment constraints, no rabies virus challenges were done, but the high concentrations (> 8 IU) of rabies neutralizing antibodies were consistent with levels that usually indicate an ability to counter the infection.
通过与用于浣熊痘病毒(RCNV)胸苷激酶基因插入失活的嵌合质粒进行同源重组,构建了一种用于预防猫泛白细胞减少症和狂犬病的重组浣熊痘病毒(RCNV)。该重组体RCN-FPV/VP2-rabG在方向相反的痘苗病毒P11启动子控制下共表达猫泛白细胞减少症病毒(FPV)VP2蛋白和狂犬病病毒糖蛋白(rabG)。用该重组体皮下接种的猫对狂犬病病毒和FPV表现出较高的中和抗体反应,并能抵御强毒FPV攻击,且白细胞计数未下降。由于实验限制,未进行狂犬病病毒攻击,但狂犬病中和抗体的高浓度(>8 IU)与通常表明具备抵抗感染能力的水平一致。