Department of Medicine, Division of Infectious Diseases, University Medical-Center Hamburg-Eppendorf , Hamburg , Germany.
Department for Clinical Immunology of Infectious Diseases, Bernhard Nocht Institute for Tropical Medicine , Hamburg , Germany.
Hum Vaccin Immunother. 2019;15(10):2269-2285. doi: 10.1080/21645515.2019.1649532. Epub 2019 Sep 5.
The devastating Ebola virus (EBOV) outbreak in West Africa in 2013-2016 has flagged the need for the timely development of vaccines for high-threat pathogens. To be better prepared for new epidemics, the WHO has compiled a list of priority pathogens that are likely to cause future outbreaks and for which R&D efforts are, therefore, paramount (R&D Blueprint: https://www.who.int/blueprint/priority-diseases/en/ ). To this end, the detailed characterization of vaccine platforms is needed. The vesicular stomatitis virus (VSV) has been established as a robust vaccine vector backbone for infectious diseases for well over a decade. The recent clinical trials testing the vaccine candidate VSV-EBOV against EBOV disease now have added a substantial amount of clinical data and suggest VSV to be an ideal vaccine vector candidate for outbreak pathogens. In this review, we discuss insights gained from the clinical VSV-EBOV vaccine trials as well as from animal studies investigating vaccine candidates for Blueprint pathogens.
2013-2016 年西非爆发的致命埃博拉病毒(EBOV)疫情表明,需要及时开发针对高威胁病原体的疫苗。为了更好地为新的传染病做好准备,世界卫生组织(WHO)编制了一份可能导致未来爆发的优先病原体清单,因此,研发工作至关重要(研发蓝图:https://www.who.int/blueprint/priority-diseases/en/)。为此,需要对疫苗平台进行详细的特征描述。囊泡性口炎病毒(VSV)已被确立为一种用于传染病的强大疫苗载体骨干,已有十多年的历史。最近针对 EBOV 疾病的疫苗候选者 VSV-EBOV 的临床试验增加了大量的临床数据,并表明 VSV 是爆发性病原体的理想疫苗载体候选者。在这篇综述中,我们讨论了从临床 VSV-EBOV 疫苗试验以及针对蓝图病原体的疫苗候选物的动物研究中获得的见解。