The MVA vector expressing the F protein of bovine respiratory syncytial virus is immunogenic in systemic and mucosal immunization routes

IF 1.8 4区 生物学 Q4 MICROBIOLOGY
Alejandra Ferella , Marina Mozgovoj , Débora Garanzini , María José Dus Santos , Gabriela Calamante , María Paula Del Médico Zajac
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引用次数: 0

Abstract

Bovine respiratory syncytial virus (BRSV) affects both beef and dairy cattle, reaching morbidity and mortality rates of 60–80% and 20%, respectively. The aim of this study was to obtain a recombinant MVA expressing the BRSV F protein (MVA-F) as a vaccine against BRSV and to evaluate the immune response induced by MVA-F after systemic immunization in homologous and heterologous vaccination (MVA-F alone or combined with a subunit vaccine), and after intranasal immunization of mice. MVA-F administered by intraperitoneal route in a homologous scheme elicited levels of neutralizing antibodies similar to those obtained with inactivated BRSV as well as better levels of IFN-γ secretion. In addition, nasal administration of MVA-F elicited local and systemic immunity with a Th1 profile. This study suggests that MVA-F is a good candidate for further evaluations combining intranasal and intramuscular routes, in order to induce local and systemic immune responses, to improve the vaccine efficacy against BRSV infection.

表达牛呼吸道合胞病毒 F 蛋白的 MVA 载体在全身和粘膜免疫途径中具有免疫原性
牛呼吸道合胞病毒(BRSV)对肉牛和奶牛都有影响,发病率和死亡率分别高达 60-80% 和 20%。本研究旨在获得表达 BRSV F 蛋白的重组 MVA(MVA-F)作为 BRSV 疫苗,并评估 MVA-F 在同源和异源(MVA-F 单独或与亚单位疫苗联合)全身免疫以及小鼠鼻内免疫后诱导的免疫反应。在同源方案中,MVA-F通过腹腔给药引起的中和抗体水平与灭活的BRSV相似,IFN-γ的分泌水平也更高。此外,鼻腔给药 MVA-F 还能激发局部和全身的 Th1 型免疫。这项研究表明,MVA-F 是一种很好的候选药物,可以结合鼻腔和肌肉注射途径进行进一步评估,以诱导局部和全身免疫反应,提高疫苗对 BRSV 感染的效力。
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来源期刊
CiteScore
3.30
自引率
0.00%
发文量
46
审稿时长
>12 weeks
期刊介绍: La Revista Argentina de Microbiología es una publicación trimestral editada por la Asociación Argentina de Microbiología y destinada a la difusión de trabajos científicos en las distintas áreas de la Microbiología. La Asociación Argentina de Microbiología se reserva los derechos de propiedad y reproducción del material aceptado y publicado.
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