多价牛呼吸道病原体疫苗对小牛体液免疫的评价

A. Berge, T. Jozan, C. Lévesque, G. Vertenten
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引用次数: 0

摘要

摘要牛呼吸道合胞病毒(BRSV)、牛副流感3型(BPI3)和溶血性曼海姆血症(Mh)是牛呼吸道疾病复合体中的主要呼吸道病原体。重要的是在生命早期优化对这些病原体的被动和主动免疫,以减少临床和亚临床生产力损失。小牛接种灭活、佐剂和多价疫苗,如Bovilis®Bovipast RSP(Bovipas)和Bovalto®Respi 3(Bovalto),可以增强对BRSV、BPI3和Mh的细胞和体液免疫。一项现场试验评估了12头接种Bovipas特和13头接种Bovalto的小牛在出生第一年对这三种药物的免疫反应,和5头阴性对照小牛。小牛从2周龄开始接种疫苗,4周后再次接种(首次接种)。大约10个月大时接种加强针。在初次接种疫苗后6个月和加强针接种后1个月的时间间隔内采集血清样本。使用血清中和测定法(SN)评估BRSV血清滴度,并且使用商业酶联免疫吸附测定法(ELISA)测试评估BRSV、BPI3和Mh滴度。通过计算Log2转化的BRSV SN滴度的曲线下面积(AUC)和BRSV、BPI3和Mh的ELISA测试的光密度测量来评估个体小牛在初次和加强疫苗接种后的血清抗体。使用多变量通用线性模型来评估疫苗接种对初次接种后6个月内血清AUC的影响。类似地,模型评估了加强疫苗接种后血清测量的AUC。与阴性对照小牛和接种Bovalto疫苗的小牛相比,接种Bovipast疫苗的小牛在初次接种和加强接种后具有显著更高的SN和ELISA滴度AUC。与阴性对照小牛相比,接种Bovalto疫苗的小牛在初次或加强疫苗接种后没有显著不同的BRSV SN和ELISA滴度AUC反应。接种疫苗的小牛对BPI3和Mh的血清抗体反应不如Bovipast BRSV抗体反应明显。Bovipast和Boval-接种小牛的BPI3和Mh的AUC ELISA OD显著更高,并且在Bovipas接种小牛中测得最高AUC。这项研究表明,小牛早期接种多价佐剂灭活BRD疫苗,如Bovilis®Bovipast RSP,可以引发具有细胞介导记忆效应的体液反应,如加强针接种所示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Field Study Evaluating Humoral Immunity in Calves Vaccinated with Multivalent Bovine Respiratory Pathogen Vaccines
Abstract Bovine Respiratory Syncytial Virus (BRSV), Bovine Parainfluenza 3 (BPI3) and Mannheimia haemolytica (Mh) are major respiratory pathogens in the bovine respiratory disease complex. It is important to optimize passive and active immunity to these pathogens early in life to reduce clinical and subclinical productivity losses. The administration of inactivated, adjuvanted and multivalent vaccines, such as Bovilis® Bovipast RSP (Bovipast), and Bovalto® Respi 3 (Bovalto) to calves, may enhance cellular and humoral immunity against BRSV, BPI3 and Mh. A field trial evaluated the immune responses to these three agents in the first year of life in 12 Bovipast and 13 Bovalto vaccinated calves, and 5 negative control calves. Calves were vaccinated starting at 2 weeks of age and revaccinated 4 weeks later (primo vaccination). A booster vaccination was given at approximately 10 months of age. Serum samples were taken at time intervals up to 6 months after primo vaccination and up to 1 month after the booster vaccination. BRSV serum titres were evaluated using a serum neutralisation assay (SN), and BRSV, BPI3 and Mh titres were evaluated using a commercial enzyme linked immunosorbent assay (ELISA) test. Serum antibodies after primo and booster vaccinations in the individual calves were evaluated by calculating the areas under the curve (AUC) of the Log2 transformed BRSV SN titres and the optic density measures of the ELISA tests for BRSV, BPI3 and Mh. Multivariate general linear models were used to evaluate the influence of the vaccination on the AUC of the serum measures within 6 months after the primo vaccination. Similarly, models evaluated the AUC of the serum measures after the booster vaccination. The Bovipast vaccinated calves had significantly higher SN and ELISA titres AUC following the primo vaccination and booster vaccinations compared to the negative control calves and the Bovalto vaccinated calves. The Bovalto vaccinated calves did not have a significantly different BRSV SN and ELISA titres AUC response after the primo or booster vaccinations compared to the negative control calves. The serum antibody responses to BPI3 and Mh in the vaccinated calves were less pronounced than the Bovipast BRSV antibody response. Bovipast and Boval- to vaccinated calves mounted a significantly higher AUC ELISA OD for both BPI3 and Mh and the highest AUC was measured in the Bovipast vaccinated calves. This study indicated that early vaccinations of calves with multivalent adjuvanted inactivated BRD vaccines, such as Bovilis® Bovipast RSP can elicit a humoral response with a cellular-mediated memory effect as indicated by the booster vaccination.
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