Current state of Ebola virus vaccines: A snapshot

Ad26, human adenovirus serotype 26; cAd3, chimpanzee adenovirus serotype 3; EBOV, Ebola virus (Zaire ebolavirus); EBOZ, Ebolavirus-Zaire species; EMA, European Medicines Agency; FDA, US Federal Drug Administration; GP, glycoprotein; i.u., infectious unit; MARV, Marburg virus; NIAID, National Immunol...

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Veröffentlicht in:PLoS pathogens 2021-12, Vol.17 (12), p.e1010078-e1010078
Hauptverfasser: Woolsey, Courtney, Geisbert, Thomas W
Format: Artikel
Sprache:eng
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Zusammenfassung:Ad26, human adenovirus serotype 26; cAd3, chimpanzee adenovirus serotype 3; EBOV, Ebola virus (Zaire ebolavirus); EBOZ, Ebolavirus-Zaire species; EMA, European Medicines Agency; FDA, US Federal Drug Administration; GP, glycoprotein; i.u., infectious unit; MARV, Marburg virus; NIAID, National Immunology Allergy and Infectious Disease; NP, nucleoprotein; PHAC, Public Health Agency of Canada; rVSV, recombinant vesicular stomatitis virus; SUDV, Sudan virus; TAFV, Taï Forest virus; ZEBOV, Zaire ebolavirus. https://doi.org/10.1371/journal.ppat.1010078.g001 [Figure omitted. Advantages and disadvantages of post-Phase I clinical trial vaccines for EBOV disease. https://doi.org/10.1371/journal.ppat.1010078.t001 Ervebo (rVSV-EBOV; V920) Ervebo is a live-attenuated, replication-competent, single-dose vaccine originally developed and shown to completely protect nonhuman primates (NHPs) by scientists at the Public Health Agency of Canada and the US Army [10]. According to preliminary results, the vaccine was 97.5% effective at stopping EBOV transmission compared to no vaccination [4]. [...]this preventive 2-dose regimen is not suitable for an outbreak response where immediate protection is necessary.
ISSN:1553-7374
1553-7366
1553-7374
DOI:10.1371/journal.ppat.1010078