Dong Fangfang, Li Dandan, Wen Dan, Li Suhua, Zhao Chaoyue, Qi Yue, Jangra Rohit K, Wu Cuiping, Xia Dequan, Zhang Xing, Deng Fei, Chandran Kartik, Zou Zhen, Yuan Fei, Zheng Aihua
1State Key Laboratory of Integrated Management of Pest Insects and Rodents, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
2University of Chinese Academy of Sciences, Beijing, China.
NPJ Vaccines. 2019 Jan 25;4:5. doi: 10.1038/s41541-018-0096-y. eCollection 2019.
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.
严重发热伴血小板减少综合征病毒(SFTSV)是一种新出现的蜱传静脉病毒,可导致人类致命疾病,目前尚无获得许可的抗病毒疫苗或疗法。在此,我们开发了一种基于减毒活重组水疱性口炎病毒(rVSV)的候选疫苗,该疫苗表达SFTSV Gn/Gc糖蛋白(rVSV-SFTSV/AH12-GP)。在免疫功能正常和免疫功能低下的小鼠中,单剂量的rVSV-SFTSV/AH12-GP可诱导产生高滴度的交叉保护性、广泛中和抗体,以对抗多种SFTSV毒株以及相关但不同的静脉病毒——哈特兰病毒(HRTV)。值得注意的是,无论是否存在预先存在的载体特异性免疫,年轻和年老的免疫功能低下小鼠均可获得针对SFTSV致死性攻击的完全保护。总体而言,这些结果表明,表达SFTSV糖蛋白的rVSV载体是一种有前景的候选疫苗,可用于对抗两种与严重人类疾病相关的新出现的静脉病毒。