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Single dose of a rVSV-based vaccine elicits complete protection against severe fever with thrombocytopenia syndrome virus

机译:单剂基于rVSV的疫苗可引发针对血小板减少症候群病毒的严重发热的完全保护

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Severe fever with thrombocytopenia virus (SFTSV) is an emerging tick-borne phlebovirus that causes lethal human disease, for which there are no licensed antiviral vaccines or therapies. Herein, we developed a live attenuated recombinant vesicular stomatitis virus (rVSV)-based vaccine candidate expressing the SFTSV Gn/Gc glycoproteins (rVSV-SFTSV/AH12-GP). High titers of cross-protective, broadly neutralizing antibodies were elicited by a single dose of rVSV-SFTSV/AH12-GP in both immunocompetent and immunocompromised mice against multiple strains of SFTSV and the related but distinct phlebovirus Heartland virus (HRTV). Remarkably, complete protection against lethal challenge with SFTSV was conferred in young and old immunocompromised mice irrespective of any pre-existing vector-specific immunity. Collectively, these results suggest that a rVSV vector expressing SFTSV glycoproteins is a promising candidate vaccine against two emerging phleboviruses associated with severe human diseases.
机译:血小板减少症病毒(SFTSV)引起的严重发烧是一种新兴的tick传静脉病毒,可引起致命的人类疾病,目前尚无许可的抗病毒疫苗或疗法。在这里,我们开发了一种表达减毒SVSV Gn / Gc糖蛋白(rVSV-SFTSV / AH12-GP)的基于减毒活体重组水疱性口炎病毒(rVSV)的候选疫苗。单剂量的rVSV-SFTSV / AH12-GP可在具有免疫力和免疫功能低下的小鼠中针对多种SFTSV菌株和相关但截然不同的静脉病毒心地病毒(HRTV)引发高滴度的交叉保护,广泛中和抗体。值得注意的是,无论是否存在预先存在的载体特异性免疫,在年轻和年老的免疫受损的小鼠中均提供了针对SFTSV致死性攻击的全面保护。总体而言,这些结果表明,表达SFTSV糖蛋白的rVSV载体是针对两种与严重人类疾病相关的新出现的静脉病毒的有前途的候选疫苗。

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