Publication:
Repeated exposure to an MF-59 adjuvanted quadrivalent subunit influenza vaccine (aQIV) in children: Results of two revaccination studies

dc.contributor.authorTimo Vesikarien_US
dc.contributor.authorK. Ramseyen_US
dc.contributor.authorP. Pitisuttithumen_US
dc.contributor.authorR. Capedingen_US
dc.contributor.authorEsther Heijnenen_US
dc.contributor.authorDaphne Sawlwinen_US
dc.contributor.authorJanine Oberyéen_US
dc.contributor.authorBin Zhangen_US
dc.contributor.authorIgor Smolenoven_US
dc.contributor.otherJanssen Vaccines & Prevention B.V.en_US
dc.contributor.otherGokilaen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherJordan Ridge Kids & Teensen_US
dc.contributor.otherSeqirus (Australia) Pty Ltden_US
dc.contributor.otherNordic Research Network Ltden_US
dc.contributor.otherSeqirus Inc.en_US
dc.contributor.otherSeqirus Netherlands B.V.en_US
dc.date.accessioned2020-11-18T08:27:26Z
dc.date.available2020-11-18T08:27:26Z
dc.date.issued2020-01-01en_US
dc.description.abstract© 2020 The Authors Background: Pediatric adjuvanted seasonal influenza vaccines induce higher immune responses and have the potential to confer better protection against influenza among young vaccine-naïve children. Limited data describe benefits and risks of repeated administration of adjuvanted influenza vaccines in children. Two revaccination studies assess the safety and immunogenicity of repeated exposure to an MF59-adjuvanted quadrivalent influenza vaccine (aQIV; Fluad®) compared to routine non-adjuvanted quadrivalent influenza vaccine (QIV). Methods: Children previously enrolled in the parent study, who received vaccination with aQIV or nonadjuvanted influenza vaccine (TIV or QIV), were recruited in Season 1 (n = 607) or Season 2 (n = 1601) of the extension trials. Season 1 participants remained in their original randomization groups (aQIV-aQIV or TIV-QIV); Season 2 subjects were re-randomized to either vaccine, resulting in four groups (aQIV-aQIV, aQIV-QIV, QIV-aQIV, or QIV-QIV). All subjects received a single-dose vaccination. Blood samples were taken for immunogenicity assessment prior to vaccination and 21 and 180 days after vaccination. Reactogenicity (Days 1–7) and safety were assessed in all subjects. Results: Hemagglutination inhibition (HI) geometric mean titer (GMT) ratios demonstrated superiority of aQIV revaccination over QIV revaccination for all strains in Season 1 and for A/H1N1, B/Yamagata, and B/Victoria in Season 2. Higher HI titers against heterologous influenza strains were observed after aQIV vaccination during both seasons. Mild to moderate severity and short duration reactogenicity was more common in the aQIV than QIV groups, but the overall safety profiles were similar to the parent study. Conclusion: The safety and immunogenicity results from this study demonstrate benefit of aQIV for both priming and revaccination of children aged 12 months to 7 years.en_US
dc.identifier.citationVaccine. (2020)en_US
dc.identifier.doi10.1016/j.vaccine.2020.10.036en_US
dc.identifier.issn18732518en_US
dc.identifier.issn0264410Xen_US
dc.identifier.other2-s2.0-85094900327en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/59907
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85094900327&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleRepeated exposure to an MF-59 adjuvanted quadrivalent subunit influenza vaccine (aQIV) in children: Results of two revaccination studiesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85094900327&origin=inwarden_US

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