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dc.contributor.authorRyan, A.L.
dc.contributor.authorWadia, U.D.
dc.contributor.authorJacoby, P.
dc.contributor.authorCheung, Laurence
dc.contributor.authorKerr, F.
dc.contributor.authorFraser, C.
dc.contributor.authorTapp, H.
dc.contributor.authorMechinaud, F.
dc.contributor.authorCarolan, L.A.
dc.contributor.authorLaurie, K.L.
dc.contributor.authorBarr, I.G.
dc.contributor.authorBlyth, C.C.
dc.contributor.authorGottardo, N.G.
dc.contributor.authorRichmond, P.C.
dc.contributor.authorKotecha, Rishi
dc.date.accessioned2020-05-18T05:39:08Z
dc.date.available2020-05-18T05:39:08Z
dc.date.issued2020
dc.identifier.citationRyan, A.L. and Wadia, U.D. and Jacoby, P. and Cheung, L.C. and Kerr, F. and Fraser, C. and Tapp, H. et al. 2020. Immunogenicity of the inactivated influenza vaccine in children who have undergone allogeneic haematopoietic stem cell transplant. Bone Marrow Transplantation. 55 (4): pp. 773-779.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/79266
dc.identifier.doi10.1038/s41409-019-0728-5
dc.description.abstract

© 2019, The Author(s), under exclusive licence to Springer Nature Limited. Influenza vaccination is recommended for children following allogeneic haematopoietic stem cell transplant (HSCT), however there is limited evidence regarding its benefit. A prospective multicentre study was conducted to evaluate the immunogenicity of the inactivated influenza vaccine in children who have undergone HSCT compared with healthy age-matched controls. Participants were vaccinated between 2013 and 2016 according to Australian guidelines. Influenza-specific hemagglutinin inhibition antibody titres were performed prior to each vaccination and 4 weeks following the final vaccination. A nasopharyngeal aspirate for influenza was performed on participants that developed influenza-like illness. There were 86 children recruited; 43 who had undergone HSCT and 43 controls. For the HSCT group, seroprotection and seroconversion rates were 81.4% and 60.5% for H3N2, 41.9% and 32.6% for H1N1, and 44.2% and 39.5% for B strain respectively. There was a significant geometric mean fold increase to the H3N2 (GMFI 5.80, 95% CI 3.68–9.14, p < 0.001) and B (GMFI 3.44, 95% CI 2.36–5.00, p = 0.048) strains. Serological response was superior in age-matched controls to all vaccine strains. There were no serious adverse events following vaccination. For children who underwent HSCT, incidence of laboratory-proven influenza infection was 2.3%. Overall, this study provides evidence to support annual inactivated influenza vaccine administration to children following HSCT.

dc.languageEnglish
dc.publisherNATURE PUBLISHING GROUP
dc.relation.sponsoredbyhttp://purl.org/au-research/grants/nhmrc/1142627
dc.relation.sponsoredbyhttp://purl.org/au-research/grants/nhmrc/1111596
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectBiophysics
dc.subjectOncology
dc.subjectHematology
dc.subjectImmunology
dc.subjectTransplantation
dc.subjectRESPIRATORY VIRUS-INFECTIONS
dc.subjectRISK-FACTORS
dc.subjectGUIDELINES
dc.subjectRECIPIENTS
dc.subjectMORTALITY
dc.subjectRESPONSES
dc.subjectIMMUNITY
dc.subjectBLOOD
dc.titleImmunogenicity of the inactivated influenza vaccine in children who have undergone allogeneic haematopoietic stem cell transplant
dc.typeJournal Article
dcterms.source.volume55
dcterms.source.number4
dcterms.source.startPage773
dcterms.source.endPage779
dcterms.source.issn0268-3369
dcterms.source.titleBone Marrow Transplantation
dc.date.updated2020-05-18T05:39:07Z
curtin.departmentSchool of Pharmacy and Biomedical Sciences
curtin.accessStatusFulltext not available
curtin.facultyFaculty of Health Sciences
curtin.contributor.orcidCheung, Laurence [0000-0001-6298-5288]
curtin.contributor.orcidKotecha, Rishi [0000-0003-1836-4075]
dcterms.source.eissn1476-5365
curtin.contributor.scopusauthoridCheung, Laurence [56663936300]


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