Reber A J, Tanner M, Okinaga T, Woolums A R, Williams S, Ensley D T, Hurley D J
Food Animal Health and Management Program, College of Veterinary Medicine, University of Georgia, Athens, GA 30602-7385, USA.
Comp Immunol Microbiol Infect Dis. 2006 Jan;29(1):61-77. doi: 10.1016/j.cimid.2006.01.001.
The development of immunity to vaccine antigen was examined using three prime/boost strategies and the progression of immune activities was evaluated over the course of 8 weeks. Calves were vaccinated and multiple immune parameters were evaluated using several methods to assess humoral or cellular immunity from the same samples in parallel. The three vaccination protocols used were a killed vaccine followed by a killed boost (killed/killed), MLV vaccine and boost (MLV/MLV), or a MLV vaccine and killed boost (MLV/killed). All the vaccines used included modified live IBR/PI3 viruses to make the bystander context as similar as possible. The Singer strain of BVDV was used as the source antigen in the killed vaccine, and the NADL strain of BVDV was used in the MLV vaccine. Controls received a vaccine containing only MLV IBR/PI3. The assessment panel measured SN titers, as well as lymphocyte proliferation, cytokine mRNA expression, intracellular cytokine production, and released IFN-gamma after in vitro stimulation with three strains of BVDV virus. MLV/MLV and MLV/killed groups developed significant SN titers to the type 1 BVDV virus strains, Singer and NADL, and low crossover titers were also seen to the type 2 strain, 890 over the evaluation period. These two groups showed significant proliferation in response to the NADL virus as compared to controls. Multiple immune assessments were conducted simultaneously to attempt to provide a broader, more in depth evaluation of immune response to these BVDV vaccination protocols. We observed that the correlation among most of the assays conducted were weak; the correlation between SN titers and cellular proliferation assays demonstrated a moderate correlation.
使用三种初免/加强免疫策略研究了对疫苗抗原的免疫发展情况,并在8周的时间内评估了免疫活性的进展。给犊牛接种疫苗,并使用几种方法评估多个免疫参数,以并行评估来自相同样本的体液免疫或细胞免疫。所使用的三种疫苗接种方案分别是灭活疫苗后加强接种灭活疫苗(灭活/灭活)、弱毒活疫苗和加强接种弱毒活疫苗(弱毒活/弱毒活),或弱毒活疫苗和加强接种灭活疫苗(弱毒活/灭活)。所有使用的疫苗都包含改良的活传染性牛鼻气管炎/牛副流感3型病毒,以使旁路途经尽可能相似。灭活疫苗中使用牛病毒性腹泻病毒(BVDV)的辛格毒株作为源抗原,弱毒活疫苗中使用BVDV的NADL毒株。对照组接种仅含弱毒活传染性牛鼻气管炎/牛副流感3型的疫苗。评估小组测量了血清中和(SN)滴度,以及淋巴细胞增殖、细胞因子mRNA表达水平、细胞内细胞因子产生情况,以及用三株BVDV病毒进行体外刺激后释放的γ干扰素。在评估期间,弱毒活/弱毒活组和弱毒活/灭活组对BVDV 1型病毒株辛格和NADL产生了显著的SN滴度,对2型毒株890也出现了低交叉滴度。与对照组相比,这两组对NADL病毒均表现出显著的增殖反应。同时进行了多项免疫评估,试图对这些BVDV疫苗接种方案的免疫反应进行更广泛、更深入的评估。我们观察到,所进行的大多数检测之间的相关性较弱;SN滴度与细胞增殖检测之间的相关性显示为中度相关。