دورية أكاديمية

Evaluation of Quil-A, E. coli DNA and Montanide™ ISA 206 adjuvant combination on the antibody response to foot-and-mouth disease vaccine in sheep.

التفاصيل البيبلوغرافية
العنوان: Evaluation of Quil-A, E. coli DNA and Montanide™ ISA 206 adjuvant combination on the antibody response to foot-and-mouth disease vaccine in sheep.
المؤلفون: Çokçalişkan, Can, Türkoğlu, Tunçer, Sareyyüpoğlu, Beyhan, Tuncer-Göktuna, Pelin, Özbilge, Banu Bayri, Uzunlu, Ergün, Kürkçü, Ayça, Uzun, Eylem Aras, Gülyaz, Veli
المصدر: Acta Virologica; 2022, Vol. 66 Issue 3, p197-205, 16p
مصطلحات موضوعية: ESCHERICHIA coli, FOOT & mouth disease, ANTIBODY formation, SHEEP diseases, DNA, SAPONINS, IMMUNOGLOBULINS
مستخلص: Vaccination is one of the basic strategies in the fight against foot-and-mouth disease (FMD) in endemic regions. Today, commercially available FMD vaccines are prepared with inactive whole virion, which has low immunogenicity. Therefore, considerable effort has been devoted to finding novel adjuvants. Although mineral oils are among the most common adjuvants, it is still difficult to provide a long-term and robust immune response. Combined adjuvant systems are currently being studied to solve the problem. Saponins and CpG-ODNs have been shown to increase the immune response to vaccines individually in various studies. In this study, the effect of different adjuvants and their combinations (Quil-A, E. coli DNA, and MontanideTM ISA 206) on total and neutralizing antibody response in sheep was investigated. According to the results, the Quil-A group induced the highest antibody level, followed by the combination of Quil-A and the E. coli DNA group. The group containing E. coli DNA also caused a higher antibody response than the group containing only MontanideTM ISA 206 for certain days of sampling. These affordable alternatives of saponin and CpG sources can be used individually to increase the potency of the FMD vaccine for mass vaccinations of sheep. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:0001723X
DOI:10.4149/av_2022_304