Dekker Aldo, Sanz-Bernardo Beatriz, Singanallur Nagendrakumar Balasubramanian, Ludi Anna B, Horsington Jacquelyn, Eblé Phaedra L, King Donald P, Vosloo Wilna
Wageningen Bioveterinary Research, P.O. Box 65, 8200 AB Lelystad, The Netherlands.
The Pirbright Institute, Ash Road, Pirbright Surrey GU24 0NF, UK.
Vaccines (Basel). 2020 Jan 14;8(1):24. doi: 10.3390/vaccines8010024.
Since 2015, outbreaks of foot-and-mouth disease (FMD) in the Middle East have been caused by a new emerging viral lineage, A/ASIA/G-VII. vaccine matching data indicated that this virus poorly matched (low r-value) with vaccines that were being used in the region as well as most other commercially available vaccines. The aim of this study was to assess the performance of two candidate vaccines against challenge with a representative field virus from the A/ASIA/G-VII lineage. The results from an initial full dose protection study provided encouraging data for the A/MAY/97 vaccine, while the A/IRQ/64 vaccine only protected 2/7 vaccinated animals. In view of these promising results, this vaccine was tested in a potency test (PD) experiment in which 5 cattle were vaccinated with a full dose, 5 cattle with a 1/3 dose and 5 cattle with a 1/9 dose of vaccine. At 21 days post vaccination these vaccinated cattle and 3 control cattle were challenged intradermolingually with a field isolate from the A/ASIA/G-VII lineage. The intra-serotype heterologous potency test resulted in an intra-serotype heterologous potency of 6.5 PD/dose. These data support previous studies showing that a high potency emergency vaccine can protect against clinical disease when challenged with a heterologous strain of the same serotype, indicating that not only the r-value of the vaccine, but also the homologous potency of a vaccine should be taken into account when advising vaccines to control an outbreak.
自2015年以来,中东地区口蹄疫(FMD)疫情一直由一种新出现的病毒谱系A/ASIA/G-VII引起。疫苗匹配数据表明,这种病毒与该地区正在使用的疫苗以及大多数其他市售疫苗的匹配性很差(r值低)。本研究的目的是评估两种候选疫苗针对来自A/ASIA/G-VII谱系的代表性田间病毒攻击的性能。初步全剂量保护研究的结果为A/MAY/97疫苗提供了令人鼓舞的数据,而A/IRQ/64疫苗仅保护了2/7的接种动物。鉴于这些有希望的结果,该疫苗在效力试验(PD)实验中进行了测试,其中5头牛接种全剂量疫苗,5头牛接种1/3剂量疫苗,5头牛接种1/9剂量疫苗。在接种疫苗后21天,这些接种牛和3头对照牛经皮内注射来自A/ASIA/G-VII谱系的田间分离株进行攻击。血清型内异源效力试验得出血清型内异源效力为6.5 PD/剂量。这些数据支持了先前的研究,表明高效力的紧急疫苗在受到相同血清型异源毒株攻击时可预防临床疾病,这表明在建议使用疫苗控制疫情时,不仅应考虑疫苗的r值,还应考虑疫苗的同源效力。