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Validation of immunity induced by inactivated CCPP vaccine with different adjuvants

机译:CCPP灭活疫苗不同佐剂诱导的免疫力验证

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The study was conducted in the premises National Veterinary Institute (NVI) to validate the immunity induced by inactivated F38 antigen adjuvated with saponin and Montanide ISA 50 and combined with and without anthrax vaccine. Post-inoculation reactions; pyrogenic effects, safety and inocuity of the vaccines were assessed. Increased body temperature and local edematous reactions were seen in animals inoculated with saponin adjuvated CCPP vaccine (100%) while 20% of the goats in ISA 50 adjuvated group showed local reaction. Sera collected from day 0 to 10th week were tested to assess the sero-conversion using monoclonal antibody based B-ELISA technique. Saponin adjuvated groups, in both monovalent CCPP and in the combined CCPP with anthrax vaccine showed a higher mean percentage of inhibition value as compared with ISA 50 adjuvated vaccine. After 8 months of post vaccination, contact challenge trial was conducted in 66 experimentally vaccinated and 20 negative control goats combined with 15 actively CCPP sick goats. Various clinical signs were recorded daily, autopsy was done on died goats and the live goats were sacrificed after 2 months of contact. The side by side samples from thoracic exudates, lung and mediastinal and bronchial lymph nodes were collected from goats shown to have developed indicative CCPP lesion for isolation and F38 antigen detection. The present experimental study indicated that application of inactivated and adjuvated CCPP vaccine significantly reduced the morbidity and development of lesions (P < 0.001). Among vaccinated groups CCPP + anthrax + saponin showed better protection, with low rate of nasal discharge and cough at 33% and 28.6%, respectively, and protection level of 94.1% from death and 65% from lung lesion development. However, the variation in protection among the vaccinated groups was not significant (P > 0.05). These findings disclosed that inactivated CCPP vaccine adjuvated with saponin and ISA 50 significantly reduce morbidity and mortality of goats due to CCPP and also indicated the importance of utilization of ISA 50 as alternative adjuvant to minimize post-vaccinal reactions encountered in use of saponin as adjuvant.
机译:这项研究是在美国国家兽医研究所(NVI)进行的,目的是验证由皂苷和Montanide ISA 50混合并结合和不结合炭疽疫苗的灭活F38抗原诱导的免疫力。接种后反应;评估了疫苗的热原作用,安全性和接种量。接种皂苷CCPP疫苗(100%)的动物体温升高和出现局部水肿反应,而ISA 50免疫组中20%的山羊表现出局部反应。使用基于单克隆抗体的B-ELISA技术测试从第0天到第10周收集的血清以评估血清转化。单价CCPP和与炭疽疫苗联合使用的CCPP中与皂苷混合的组均比ISA 50混合疫苗具有更高的平均抑制率。接种疫苗后8个月后,对66例进行了疫苗接种的实验性山羊和20例阴性对照山羊与15例患有CCPP的活跃山羊进行了接触挑战试验。每天记录各种临床体征,对死亡的山羊进行尸检,并在接触2个月后处死活山羊。从山羊身上收集了胸腔分泌物,肺以及纵隔和支气管淋巴结的并排样品,这些山羊显示出具有指示性的CCPP病变,可用于分离和F38抗原检测。目前的实验研究表明,灭活和灭活的CCPP疫苗的使用显着降低了病变的发病率和发展(P <0.001)。在接种疫苗的人群中,CCPP +炭疽+皂苷显示出更好的保护作用,鼻涕和咳嗽的发生率较低,分别为33%和28.6%,对死亡的保护水平为94.1%,对肺部病变的保护水平为65%。但是,接种组之间的保护差异并不显着(P> 0.05)。这些发现表明,与皂苷和ISA 50结合使用的灭活CCPP疫苗可显着降低山羊由于CCPP引起的发病率和死亡率,并且还表明了利用ISA 50作为替代佐剂的重要性,以最大程度地减少使用皂素作为佐剂的疫苗接种后反应。

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