The Journal of infectious diseases · 2018
A Replicating Single-Cycle Adenovirus Vaccine Against Ebola Virus.
СтатьяПоддержка NIH: внешняя программаResearch Support, N.I.H., IntramuralПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Anguiano-Zarate Stephanie S, Matchett William E, Nehete Pramod N, Sastry Jagannadha K, Marzi Andrea, Barry Michael A
Аннотация
Recent West African Ebola virus (EBOV) epidemics have led to testing different anti-EBOV vaccines, including a replication-defective adenovirus (RD-Ad) vector (ChAd3-EBOV) and an infectious, replication-competent recombinant vesicular stomatitis virus expressing the EBOV glycoprotein (rVSV-EBOV; also known as rVSV-ZEBOV). While RD-Ads elicit protection, when scaled up to human trials, the level of protection may be much lower than that of vaccines containing viruses that can replicate. Although a replication-competent Ad (RC-Ad) vaccine might generate a level of protection approximating that of rVSV, this infectious vector would also risk causing adenovirus disease. We recently described a "single-cycle" adenovirus (SC-Ad) vector that amplifies antigen genes like RC-Ad, but that avoids the risk of adenovirus infection. Here we have tested an SC-Ad6 vector expressing the glycoprotein (GP) from a 2014 EBOV strain in mice, hamsters, and rhesus macaques. We show that SC-Ad6-EBOV GP induces a high level of serum antibodies in all species and mediates significant protection against pseudo-challenge with rVSV-EBOV expressing luciferase in mice and hamsters. These data suggest that SC-Ad6-EBOV GP may be useful during future EBOV outbreaks.
Предметные рубрики MeSH
A549 CellsAdenoviridaeAgingAnimalsAntibodies, ViralChlorocebus aethiopsCricetinaeDose-Response Relationship, ImmunologicEbola VaccinesEbolavirusEnzyme-Linked Immunosorbent AssayFemaleGlycoproteinsHEK293 CellsHemorrhagic Fever, EbolaHumansImmunization ScheduleMacaca mulattaMesocricetusMiceVaccines, SyntheticVero CellsVirus Replication