Vaccine and Infectious Disease Organization - International Vaccine Centre, VIDO-InterVac, 120 Veterinary Rd., Saskatoon, SK S7N 5E3, Canada.
Vaccine and Infectious Disease Organization - International Vaccine Centre, VIDO-InterVac, 120 Veterinary Rd., Saskatoon, SK S7N 5E3, Canada.
Vaccine. 2017 Dec 4;35(48 Pt B):6604-6610. doi: 10.1016/j.vaccine.2017.10.037. Epub 2017 Oct 24.
Prevention and or control of Mycoplasma bovis infections in cattle have relied on the treatment of animals with antibiotics; herd management including separation and or culling infected animals; and the use of vaccines with limited protection. Due to the negative reactions and incomplete protection observed after vaccination with some bacterin-based vaccines, there is a need to put more efforts in the development of recombinant-based vaccines. However, the arsenal of antigens that may be suitable for a fully protective vaccine is rather limited at this point. We have tested a vaccine formulation containing M. bovis proteins formulated with adjuvants that have been shown to aid in the protection against other pathogens. After vaccinations, the animals were challenged using a BHV-1/M. bovis co-infection model. While the PBMC proliferation and cytokine responses to the antigens in the vaccine were negligible, humoral responses reveal that eight antigens elicit a balanced IgG1/IgG2 response although this was not enough to confer protection against M. bovis.
牛支原体感染的预防和/或控制依赖于对动物使用抗生素进行治疗;包括分离和/或淘汰感染动物的畜群管理;以及使用具有有限保护作用的疫苗。由于一些基于菌体制剂的疫苗接种后观察到的负面反应和不完全保护作用,因此需要在重组疫苗的开发方面投入更多的努力。然而,在这一点上,适合完全保护性疫苗的抗原库相当有限。我们已经测试了一种含有牛支原体蛋白的疫苗配方,该配方与已证明有助于抵抗其他病原体的佐剂一起配制。接种疫苗后,使用 BHV-1/牛支原体共感染模型对动物进行了挑战。虽然 PBMC 对疫苗中抗原的增殖和细胞因子反应可以忽略不计,但体液反应表明,有 8 种抗原引起了平衡的 IgG1/IgG2 反应,尽管这还不足以提供针对牛支原体的保护。