Development of a SFTSV DNA vaccine that confers complete protection against lethal infection in ferrets.
Jeong-Eun KwakYoung-Il KimSu-Jin ParkMin-Ah YuHyeok-Il KwonSukyeong EoTae-Shin KimJoon SeokWon-Suk ChoiJu Hwan JeongHyojin LeeYoungran ChoJin Ah KwonMoonsup JeongJoel N MaslowYong-Eun KimHaili JeonKee K KimEui-Cheol ShinMin-Suk SongJae U JungDavid Hyunjung ChungSu-Hyung ParkPublished in: Nature communications (2019)
Although the incidence of severe fever with thrombocytopenia syndrome virus (SFTSV) infection has increased from its discovery with a mortality rate of 10-20%, no effective vaccines are currently available. Here we describe the development of a SFTSV DNA vaccine, its immunogenicity, and its protective efficacy. Vaccine candidates induce both a neutralizing antibody response and multifunctional SFTSV-specific T cell response in mice and ferrets. When the vaccine efficacy is investigated in aged-ferrets that recapitulate fatal clinical symptoms, vaccinated ferrets are completely protected from lethal SFTSV challenge without developing any clinical signs. A serum transfer study reveals that anti-envelope antibodies play an important role in protective immunity. Our results suggest that Gn/Gc may be the most effective antigens for inducing protective immunity and non-envelope-specific T cell responses also can contribute to protection against SFTSV infection. This study provides important insights into the development of an effective vaccine, as well as corresponding immune parameters, to control SFTSV infection.