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dc.contributor.authorDarpel, Karin E.
dc.contributor.authorCorla, Amanda
dc.contributor.authorStedman, Anna
dc.contributor.authorBellamy, Fiona
dc.contributor.authorFlannery, John
dc.contributor.authorRajko-Nenow, Paulina
dc.contributor.authorPowers, Claire
dc.contributor.authorWilson, Steve
dc.contributor.authorCharleston, Bryan
dc.contributor.authorBaron, Michael D.
dc.contributor.authorBatten, Carrie
dc.date.accessioned2024-11-27T14:56:13Z
dc.date.available2024-11-27T14:56:13Z
dc.date.copyright2024
dc.date.issued2024-06-03
dc.identifier.citationDarpel, K.E., Corla, A., Stedman, A. et al. (2024) 'Long-term trial of protection provided by adenovirus-vectored vaccine expressing the PPRV H protein'. npj Vaccines, 9, 98. Available at: https://doi.org/10.1038/s41541-024-00892-2en_US
dc.identifier.issn2059-0105
dc.identifier.urihttps://research.thea.ie/handle/20.500.12065/4864
dc.description.abstractA recombinant, replication-defective, adenovirus-vectored vaccine expressing the H surface glycoprotein of peste des petits ruminants virus (PPRV) has previously been shown to protect goats from challenge with wild-type PPRV at up to 4 months post vaccination. Here, we present the results of a longer-term trial of the protection provided by such a vaccine, challenging animals at 6, 9, 12 and 15 months post vaccination. Vaccinated animals developed high levels of anti-PPRV H protein antibodies, which were virus-neutralising, and the level of these antibodies was maintained for the duration of the trial. The vaccinated animals were largely protected against overt clinical disease from the challenge virus. Although viral genome was intermittently detected in blood samples, nasal and/or ocular swabs of vaccinated goats post challenge, viral RNA levels were significantly lower compared to unvaccinated control animals and vaccinated goats did not appear to excrete live virus. This protection, like the antibody response, was maintained at the same level for at least 15 months after vaccination. In addition, we showed that animals that have been vaccinated with the adenovirus-based vaccine can be revaccinated with the same vaccine after 12 months and showed an increased anti-PPRV antibody response after this boost vaccination. Such vaccines, which provide a DIVA capability, would therefore be suitable for use when the current live attenuated PPRV vaccines are withdrawn at the end of the ongoing global PPR eradication campaign.en_US
dc.formatapplication/pdfen_US
dc.language.isoengen_US
dc.publisherNature Researchen_US
dc.relation.ispartofnpj Vaccinesen_US
dc.rightsAttribution 4.0 International*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subjectinfectionen_US
dc.subjectvaccineen_US
dc.titleLong-term trial of protection provided by adenovirus-vectored vaccine expressing the PPRV H proteinen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.contributor.affiliationTechnological University of the Shannon: Midlands Midwesten_US
dc.description.peerreviewyesen_US
dc.identifier.doi10.1038/s41541-024-00892-2en_US
dc.identifier.startpage98en_US
dc.identifier.volume9en_US
dc.rights.accessrightsinfo:eu-repo/semantics/openAccessen_US
dc.subject.departmentDepartment of Pharmaceutical Sciences and Biotechnologyen_US
dc.type.versioninfo:eu-repo/semantics/publishedVersionen_US


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Attribution 4.0 International
Except where otherwise noted, this item's license is described as Attribution 4.0 International