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评估加拿大西部异源和同源初免-加强免疫接种肉牛犊牛中牛呼吸道合胞体病毒(BRSV)和牛疱疹病毒(BHV)特异性抗体反应。

Evaluation of bovine respiratory syncytial virus (BRSV) and bovine herpesvirus (BHV) specific antibody responses between heterologous and homologous prime-boost vaccinated western Canadian beef calves.

机构信息

Department of Large Animal Clinical Sciences (Erickson, Berenik, Campbell, Gow, Waldner), Department of Microbiology (Lacoste, Ellis), Western College of Veterinary Medicine, University of Saskatchewan, 52 Campus Drive, Saskatoon, Saskatchewan S7N 5B4; Department of Animal and Poultry Science, College of Agriculture and Bioresources, University of Saskatchewan, 51 Campus Drive, Saskatoon, Saskatchewan S7N 5A8 (Lardner).

出版信息

Can Vet J. 2021 Jan;62(1):37-44.

Abstract

Bovine respiratory disease (BRD) is an economically important cause of morbidity and mortality in beef calves. Control of BRD is most often addressed through "homologous" vaccination utilizing the same injectable modified-live viral (MLV) vaccine for both priming and boosting. Heterologous prime-boosting uses different routes and antigenic forms for priming and boosting. Three vaccine protocols were compared: an injectable (IJ) MLV (IJ-MLV) group (IJ-MLV priming at ~48 days and boosted with IJ-MLV at weaning), intranasal (IN) MLV (IN-MLV) group (intranasal priming with MLV at ~24 hours, boosted twice with an IJ-MLV), and intranasal killed viral (IN-KV) group (primed with an IN-MLV at ~24 hours, boosted twice with an IJ-KV). Serum antibody concentrations determined by enzyme-linked immunosorbent assays (ELISAs) were compared and the IN-KV group had significantly higher BRSV-specific antibody concentrations after boosting compared with the 2 homologous groups. No differences in BHV-specific antibody concentrations were observed between any of the groups.

摘要

牛呼吸道疾病(BRD)是导致肉牛犊发病率和死亡率的重要经济原因。BRD 的控制通常通过“同源”疫苗接种来实现,即使用相同的注射用改良活病毒(MLV)疫苗进行初免和加强免疫。异源初免加强则采用不同的途径和抗原形式进行初免和加强免疫。比较了三种疫苗方案:注射用(IJ)MLV(IJ-MLV)组(在约 48 天时进行 IJ-MLV 初免,在断奶时用 IJ-MLV 加强免疫)、鼻内(IN)MLV(IN-MLV)组(在约 24 小时时用 MLV 进行鼻内初免,用 IJ-MLV 进行两次加强免疫)和鼻内灭活病毒(IN-KV)组(在约 24 小时时用 IN-MLV 进行初免,用 IJ-KV 进行两次加强免疫)。通过酶联免疫吸附测定(ELISA)比较血清抗体浓度,加强免疫后,IN-KV 组的 BRSV 特异性抗体浓度明显高于 2 个同源组。各组之间均未观察到 BHV 特异性抗体浓度的差异。

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