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首页> 外文期刊>Vaccine >Foot-and-mouth disease vaccine potency testing: The influence of serotype, type of adjuvant, valency, fractionation method, and virus culture on the dose-response curve in cattle
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Foot-and-mouth disease vaccine potency testing: The influence of serotype, type of adjuvant, valency, fractionation method, and virus culture on the dose-response curve in cattle

机译:口蹄疫疫苗效价测试:血清型,佐剂类型,效价,分离方法和病毒培养对牛剂量反应曲线的影响

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摘要

The aim of this study was to determine a relationship between vaccine potency (amount of PD(50) per dose) and fraction of clinically protected cattle following homologous challenge with infectious foot-and-mouth disease (FMD) virus, and to determine the effect of method of fractionation, serotype, type of adjuvant, valency and type of virus culture on the dose-response curve. Data from 297 potency tests of FMD vaccines, comprising 4004 vaccinated cattle, performed at the FMD vaccine production facility in the Netherlands, were used for the present study. A generalised linear mixed effect model was used to analyse the results. Our study showed that the relation between FMD vaccine potency and fraction protected was also affected by the serotype and type of adjuvant. No common level of protection could be assigned to all FMD vaccines with the same amount of PD(50) per dose, this information is essential when designing a new standard FMD vaccines control.
机译:这项研究的目的是确定疫苗效力(每剂PD(50)的量)与感染口蹄疫(FMD)病毒的同源攻击后临床保护牛的比例之间的关系,并确定其效果剂量反应曲线上分离方法,血清型,佐剂类型,效价和病毒培养类型的比较在本研究中,使用了在荷兰的FMD疫苗生产设施进行的297口FMD疫苗效力测试的数据,其中包括4004头牛疫苗接种。使用广义线性混合效应模型来分析结果。我们的研究表明,FMD疫苗效力与保护级分之间的关​​系也受到佐剂的血清型和类型的影响。没有为每个口蹄疫疫苗分配相同剂量的PD(50)的通用保护级别,在设计新的标准口蹄疫疫苗对照时,此信息必不可少。

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