Colorado State University Department of Biomedical Sciences, Foothills Campus, Fort Collins, CO 80523, USA.
Summit Research, 4010 Buoy Boulevard, Helena, MT 59602, USA.
Vaccine. 2014 Sep 22;32(42):5455-9. doi: 10.1016/j.vaccine.2014.07.093. Epub 2014 Aug 12.
Over the last years West Nile virus (WNV) lineage 2 has spread from the African to the European continent. This study was conducted to demonstrate efficacy of an inactivated, lineage 1-based, WNV vaccine (Equip WNV) against intrathecal challenge of horses with a recent isolate of lineage 2 WNV. Twenty horses, sero-negative for WNV, were enrolled and were randomly allocated to one of two treatment groups: an unvaccinated control group (T01, n=10) and a group administered with Equip WNV (T02, n=10). Horses were vaccinated at Day 0 and 21 and were challenged at day 42 with WNV lineage 2, Nea Santa/Greece/2010. Personnel performing clinical observations were blinded to treatment allocation. Sixty percent of the controls had to be euthanized after challenge compared to none of the vaccinates. A significantly lower percentage of the vaccinated animals showed clinical disease (two different clinical observations present on the same day) on six different days of study and the percentage of days with clinical disease was significantly lower in the vaccinated group. A total of 80% of the non-vaccinated horses showed viremia while only one vaccinated animal was positive by virus isolation on a single occasion. Vaccinated animals started to develop antibodies against WNV lineage 2 from day 14 (2 weeks after the first vaccination) and at day 42 (the time of onset of immunity) they had all developed a strong antibody response. Histopathology scores for all unvaccinated animals ranged from mild to very severe in each of the tissues examined (cervical spinal cord, medulla and pons), whereas in vaccinated horses 8 of 10 animals had no lesions and 2 had minimal lesions in one tissue. In conclusion, Equip WNV significantly reduced the number of viremic horses, the duration and severity of clinical signs of disease and mortality following challenge with lineage 2 WNV.
在过去的几年中,西尼罗河病毒(WNV)谱系 2 已从非洲传播到欧洲大陆。本研究旨在证明基于谱系 1 的灭活 WNV 疫苗(Equip WNV)对用最近分离的谱系 2 WNV 进行鞘内挑战的马的功效。将 20 匹血清学上对 WNV 为阴性的马纳入研究,并随机分配到两个治疗组之一:未接种疫苗的对照组(T01,n=10)和接种 Equip WNV 的组(T02,n=10)。马匹在第 0 天和第 21 天接种疫苗,并在第 42 天用 WNV 谱系 2,Nea Santa/Greece/2010 进行挑战。进行临床观察的人员对治疗分配进行了盲法。与接种疫苗的动物相比,对照组中有 60%的动物在挑战后必须安乐死,而接种疫苗的动物中无一例出现这种情况。接种疫苗的动物在研究的六天中有六天出现不同的临床症状(同一天出现两种不同的临床观察),并且接种疫苗的动物的临床疾病天数明显减少。未接种疫苗的马中有 80%出现病毒血症,而只有一只接种疫苗的动物在一次检测中呈阳性。接种疫苗的动物从第 14 天(第一次接种后 2 周)开始产生针对 WNV 谱系 2 的抗体,并且在第 42 天(免疫开始时),它们都产生了强烈的抗体反应。所有未接种疫苗的动物在每个检查的组织中均表现出从轻度到非常严重的组织病理学评分(颈脊髓、延髓和脑桥),而在接种疫苗的马中,10 只中有 8 只没有病变,2 只在一个组织中有轻微病变。总之,Equip WNV 显著减少了病毒血症马的数量、疾病临床症状的持续时间和严重程度以及谱系 2 WNV 挑战后的死亡率。