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由Vnukovo-32/107毒株制备的实验性口服狂犬病疫苗的免疫原性和抗原活性

Immunogenic and antigenic activity of an experimental oral rabies vaccine prepared from the strain Vnukovo-32/107.

作者信息

Svrcek S, Durove A, Ondrejka R, Závadová J, Süliová J, Benísek Z, Vrtiak O J, Feketeová J, Mad'ar M

机构信息

Rabiological Laboratory, University of Veterinary Medicine, Kosice, Slovak Republic.

出版信息

Vet Med (Praha). 1995 Mar;40(3):87-96.

PMID:7762124
Abstract

The immunogenic and antigenic activity of an experimental live oral rabies vaccine prepared from the strain Vnukovo-32/107 was evaluated on the basis of results obtained in 3 sets of experiments. These were carried out as model experiments on white mice, then on target animals--red foxes (Vulpes vulpes) and a related species--farm-bred polar foxes (Alopex lagopus). For quantitative determination of the immunogenic activity of the orally or subcutaneously administered rabies vaccines in model experiments on mice a method was used that had been developed in our laboratory. Antibodies were detected and quantified by an ELISA kit that had also been developed in our lab. Tenacity of the experimental vaccine (infectious tissue culture medium after yolk addition) was verified at different temperatures; the effects of storage temperature upon virus titre and immunogenic activity were investigated. An important part of the experiments--evaluation of the antigenic and immunogenic activity of the live vaccine at oral vaccination (vaccination baits, conditions simulating field vaccination) was carried out in foxes. The immunogenic activity (challenge experiments with a street virus on day 180 and 360 after vaccination) was evaluated in common foxes (Vulpes vulpes). The results document a high immunogenic and antigenic activity of the experimental live oral rabies vaccine. The strain Vnukovo-32/107 is suitable for the industrial manufacturing of vaccination baits. In the target species--common foxes challenged on day 180 after primovaccination an 83% protection was observed. Challenge on day 180 after revaccination (or day 360 after primovaccination), the orally immunized foxes proved to be 100% protected. For parallel evaluation of the immunogenic activity of an oral vaccine and for antibody titration it is recommended to employ the quantitative mice test and an ELISA technique, respectively.

摘要

根据3组实验结果,对用Vnukovo - 32/107毒株制备的实验性口服狂犬病活疫苗的免疫原性和抗原活性进行了评估。这些实验首先在白色小鼠身上作为模型实验开展,然后在目标动物——赤狐(Vulpes vulpes)和相关物种——养殖北极狐(Alopex lagopus)身上进行。在小鼠模型实验中,采用我们实验室开发的方法对口服或皮下接种的狂犬病疫苗的免疫原性活性进行定量测定。通过同样在我们实验室开发的ELISA试剂盒检测和定量抗体。在不同温度下验证了实验疫苗(添加蛋黄后的感染性组织培养基)的稳定性;研究了储存温度对病毒滴度和免疫原性活性的影响。实验的一个重要部分——在狐狸身上评估口服疫苗(疫苗诱饵,模拟野外接种条件)时活疫苗的抗原性和免疫原性活性。在普通狐狸(Vulpes vulpes)身上评估免疫原性活性(接种后第180天和第360天用街毒株进行攻击实验)。结果证明实验性口服狂犬病活疫苗具有高免疫原性和抗原活性。Vnukovo - 32/107毒株适合用于工业生产疫苗诱饵。在目标物种——初免后第180天接受攻击的普通狐狸中,观察到83%的保护率。再次接种后第180天(或初免后第360天)进行攻击时,口服免疫的狐狸被证明100%受到保护。为了平行评估口服疫苗的免疫原性活性和进行抗体滴定,建议分别采用定量小鼠试验和ELISA技术。

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