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Application of non-structural protein antibody tests in substantiating freedom from foot-and-mouth disease virus infection after emergency vaccination of cattle

机译:非结构蛋白抗体测试在证实牛紧急接种疫苗后免于口蹄疫病毒感染的应用

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There has been much debate about the use of the so-called "vaccinate-to-live" policy for the control of foot-and-mouth disease (FMD) in Europe, according to which, spread of the FMD virus (FMDV) from future outbreaks could be controlled by a short period of "emergency" vaccination of surrounding herds, reducing the need for large-scale preemptive culling of at-risk animals. Since vaccinated animals may become subclinically infected with FMDV following challenge exposure, it is necessary to either remove all vaccinates (vaccinate-to-kill) or to detect and remove vaccinates in which virus is circulating or has established persistent infections (vaccinate-to-live), in order to rapidly regain the most favoured trading status of FMD-free without vaccination. The latter approach can be supported by testing vaccinated animals for the presence of antibodies to certain non-structural proteins (NSP) of FMDV, which are induced by infection with the virus, but not by vaccination with purified FMD vaccines. Using test sensitivity and specificity data established at a recent workshop on NSP assays [Brocchi E, Bergmann I, Dekker A, Paton DJ, Sammin DJ, Greiner M, et al. Comparative performance of six ELISAs for antibodies to the non-structural proteins of foot-and-mouth disease. Vaccine, in press], this paper examines the ways in which serological testing with NSP ELISAs can be used and interpreted and the effect that this will have on the confidence with which freedom from infection can be demonstrated within guidelines specified by the World Animal Health Organisation and the European Commission.
机译:关于使用所谓的“活疫苗”政策控制欧洲口蹄疫(FMD)的争论一直很多,据此,口蹄疫病毒(FMDV)的传播源于未来的暴发可以通过对周围畜群进行短期“紧急”疫苗接种来控制,从而减少了对有风险的动物进行大规模先发性扑杀的需求。由于接种疫苗的动物在暴露于挑战后可能会被FMDV亚临床感染,因此有必要要么清除所有疫苗(杀死疫苗),要么检测并清除病毒在其中传播或已经建立持续感染的疫苗(存活疫苗) ),以便迅速恢复无疫苗接种免费口蹄疫的最惠国待遇。后一种方法可以通过测试疫苗接种的动物是否存在针对FMDV的某些非结构蛋白(NSP)的抗体来支持,该抗体是通过病毒感染而不是通过纯化的FMD疫苗接种而诱导的。使用在NSP分析的最新研讨会上建立的测试敏感性和特异性数据[Brocchi E,Bergmann I,Dekker A,Paton DJ,Sammin DJ,Greiner M等。六种ELISA方法对口蹄疫非结构蛋白抗体的比较性能。 [正在出版的疫苗],本文探讨了使用和解释NSP ELISA进行血清学检测的方式,以及这将对在世界动物卫生组织指定的指南中证明无感染的信心产生的影响和欧洲委员会。

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