Preparation and field study of combined vaccine against Clostridium perfringens type A and bovine viral diarrhea virus in camels

IF 2.1 Q4 IMMUNOLOGY
H. Elhelw, Maha Raafat Abd el Fadeel, E. El-Sergany, A. Allam, M. K. Elbayoumy, A. El-Kattan, A. A. El-Kholy
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引用次数: 2

Abstract

Purpose The key objective of this study was to formulate a local combined inactivated gel adjuvanted vaccine containing bovine viral diarrhea virus (BVDV)-1, BVDV-2 viruses and Clostridium perfringens type A toxoid. The study evaluated its ability to enhance protective active immune response in camels’ calves against these infectious pathogens under field conditions. Materials and Methods The local BVDV cytopathic strains and a local strain of toxigenic C. perfringens type A were used in vaccines formulation. Vaccines A and B were monovalent vaccines against C. perfringens and both strains of BVDVs, respectively. While the vaccine C was the combined vaccine used against the three agents. All vaccines were adjuvanted with Montanide gel. Sterility, safety, and potency tests were applied on the formulated vaccines. Virus neutralization and toxin anti-toxin neutralization tests were used to evaluate the immune responses. Results Both monovalent (vaccine A) and combined vaccines (vaccine C) showed a protective level (4.5 and 3 IU/mL, respectively) against C. perfringens from the 2nd-week post-vaccination. The titer declined to 3 and 2 IU/mL, respectively at the 5th-month post-vaccination. The titer against BVDV, the monovalent vaccine (vaccine B) reached the beak (1.95 IU/mL) at the 1st-month post-vaccination and lasted till 6th-month post-vaccination (0.92 and 0.94 IU/mL) for BVDV-1a and BVDV-2, respectively. Conclusion Vaccination of camels with the combined vaccine adjuvanted by Montanide gel containing C. perfringens type A toxoid and BVDV strains with 6-month intervals is recommended to protect camels safely and efficiently against such infections in the field.
骆驼产气荚膜梭状芽孢杆菌和牛病毒性腹泻联合疫苗的制备及现场研究
目的本研究的主要目的是研制一种含有牛病毒性腹泻病毒(BVDV)-1、BVDV-2和产气荚膜梭菌a型类毒素的局部联合灭活凝胶佐剂疫苗。该研究评估了其在野外条件下增强骆驼幼崽对这些传染性病原体的保护性主动免疫反应的能力。材料与方法采用BVDV细胞病变株和产毒产气荚膜梭菌a型的地方株进行疫苗配制。疫苗A和B分别是针对产气荚膜梭菌和两种BVDV菌株的单价疫苗。而疫苗C是针对这三种药物使用的联合疫苗。所有的疫苗都用Montanide凝胶作为佐剂。对配制的疫苗进行了无菌性、安全性和效力测试。病毒中和试验和毒素-毒素-抗毒素中和试验用于评估免疫反应。结果从接种后第2周起,单价疫苗(疫苗A)和联合疫苗(疫苗C)对产气荚膜梭菌的保护水平分别为4.5和3IU/mL。接种后第5个月,滴度分别降至3和2 IU/mL。单价疫苗(疫苗B)对BVDV-1a和BVDV-2的抗BVDV滴度分别在接种后1个月达到喙部(1.95 IU/mL)和持续到接种后6个月(0.92和0.94 IU/mL)。结论建议采用含产气荚膜梭菌A型类毒素和BVDV株的Montanide凝胶联合疫苗,间隔6个月对骆驼进行接种,以安全有效地保护骆驼免受此类感染。
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来源期刊
CiteScore
3.70
自引率
3.70%
发文量
29
审稿时长
8 weeks
期刊介绍: Clin Exp Vaccine Res, the official English journal of the Korean Vaccine Society, is an international, peer reviewed, and open-access journal. It covers all areas related to vaccines and vaccination. Clin Exp Vaccine Res publishes editorials, review articles, special articles, original articles, case reports, brief communications, and correspondences covering a wide range of clinical and experimental subjects including vaccines and vaccination for human and animals against infectious diseases caused by viruses, bacteria, parasites and tumor. The scope of the journal is to disseminate information that may contribute to elaborate vaccine development and vaccination strategies targeting infectious diseases and tumors in human and animals. Relevant topics range from experimental approaches to (pre)clinical trials for the vaccine research based on, but not limited to, basic laboratory, translational, and (pre)clinical investigations, epidemiology of infectious diseases and progression of all aspects in the health related issues. It is published printed and open accessed online issues (https://ecevr.org) two times per year in 31 January and 31 July. Clin Exp Vaccine Res is linked to many international databases and is made freely available to institutions and individuals worldwide
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