Tabynov Kaissar, Yespembetov Bolat, Matikhan Nurali, Ryskeldinova Sholpan, Zinina Nadezhda, Kydyrbayev Zhailaubay, Assanzhanova Nurika, Tabynov Kairat, Renukaradhya Gourapura J, Mukhitdinova Gulnara, Sansyzbay Abylai
The Research Institute for Biological Safety Problems, Zhambulskaya oblast, Kordaiskiy rayon, 080409, Gvardeiskiy, Kazakhstan.
The Research Institute for Biological Safety Problems, Zhambulskaya oblast, Kordaiskiy rayon, 080409, Gvardeiskiy, Kazakhstan.
Vet Microbiol. 2016 Dec 25;197:15-20. doi: 10.1016/j.vetmic.2016.11.001. Epub 2016 Nov 3.
Previously we developed and evaluated a candidate influenza viral vector based Brucella abortus vaccine (Flu-BA) administered with a potent adjuvant Montanide Gel01 in cattle, which was found safe and highly effective. This study was aimed to establish a proof-of-concept of the efficacy of Flu-BA vaccine formulation in sheep and goats. We vaccinated sheep and goats with Flu-BA vaccine and as a positive control vaccinated a group of animals with a commercial B. melitensis Rev.1 vaccine. Clinically, both Flu-BA and Rev.1 vaccines were found safe. Serological analysis showed the animals received Flu-BA vaccine did not induce antibody response against Brucella Omp16 and L7/L12 proteins during the period of our study (56days post-initial vaccination, PIV). But observed significant antigen-specific T cell response indicated by increased lymphocyte stimulation index and enhanced secretion of IFN-γ at day 56 PIV in Flu-BA group. The Flu-BA vaccinated animals completely protected 57.1% of sheep and 42.9% of goats against B. melitensis 16M challenge. The severity of brucellosis in terms of infection index and colonization of Brucella in tissues was significantly lower in the Flu-BA group compared to negative control animals group. Nevertheless, positive control commercial Rev.1 vaccine provided strong antigen-specific T cell immunity and protection against B. melitensis 16M infection. We conclude that the Flu-BA vaccine induces a significant antigen-specific T-cell response and provides complete protection in approximately 50% of sheep and goats against B. melitensis 16M infection. Further investigations are needed to improve the efficacy of Flu-BA and explore its practical application in small ruminants.
此前,我们研发并评估了一种基于流感病毒载体的牛流产布鲁氏菌疫苗(Flu-BA),该疫苗与强效佐剂Montanide Gel01联合用于牛,结果显示其安全且高效。本研究旨在验证Flu-BA疫苗制剂在绵羊和山羊中的有效性概念。我们用Flu-BA疫苗对绵羊和山羊进行免疫接种,并作为阳性对照,用一种商业性的羊种布鲁氏菌Rev.1疫苗对一组动物进行免疫接种。在临床上,Flu-BA和Rev.1疫苗均被证明是安全的。血清学分析表明,在我们的研究期间(初次接种疫苗后56天,PIV),接受Flu-BA疫苗接种的动物未诱导出针对布鲁氏菌Omp16和L7/L12蛋白的抗体反应。但观察到显著的抗原特异性T细胞反应,表现为在PIV第56天时Flu-BA组淋巴细胞刺激指数增加以及IFN-γ分泌增强。接种Flu-BA疫苗的动物使57.1%的绵羊和42.9%的山羊完全抵御了羊种布鲁氏菌16M的攻击。与阴性对照动物组相比,Flu-BA组布鲁氏菌病在感染指数和组织中布鲁氏菌定植方面的严重程度显著更低。然而,阳性对照商业Rev.1疫苗提供了强大的抗原特异性T细胞免疫力,并能抵御羊种布鲁氏菌16M感染。我们得出结论,Flu-BA疫苗可诱导显著的抗原特异性T细胞反应,并能为约50%的绵羊和山羊提供针对羊种布鲁氏菌16M感染的完全保护。需要进一步研究以提高Flu-BA的效力,并探索其在小型反刍动物中的实际应用。