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dc.contributor.authorFaustini, SE
dc.contributor.authorHall, A
dc.contributor.authorBrown, S
dc.contributor.authorRoberts, S
dc.contributor.authorHill, H
dc.contributor.authorStamataki, Z
dc.contributor.author(PITCH) consortium,
dc.contributor.authorJenner, MW
dc.contributor.authorOwen, RG
dc.contributor.authorPratt, G
dc.contributor.authorCook, G
dc.contributor.authorRichter, A
dc.contributor.authorDrayson, MT
dc.contributor.authorKaiser, MF
dc.contributor.authorHeaney, JLJ
dc.coverage.spatialEngland
dc.date.accessioned2023-06-02T10:28:00Z
dc.date.available2023-06-02T10:28:00Z
dc.date.issued2023-06-01
dc.identifier.citationBritish Journal of Haematology, 2023, 201 (5), pp. 845 - 850
dc.identifier.issn0007-1048
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5824
dc.identifier.eissn1365-2141
dc.identifier.eissn1365-2141
dc.identifier.doi10.1111/bjh.18714
dc.description.abstractMultiple myeloma (MM) and anti-MM therapy cause profound immunosuppression, leaving patients vulnerable to coronavirus disease 2019 (COVID-19) and other infections. We investigated anti-severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) antibodies longitudinally in ultra-high-risk patients with MM receiving risk-adapted, intensive anti-CD38 combined therapy in the Myeloma UK (MUK) nine trial. Despite continuous intensive therapy, seroconversion was achieved in all patients, but required a greater number of vaccinations compared to healthy individuals, highlighting the importance of booster vaccinations in this population. Reassuringly, high antibody cross-reactivity was found with current variants of concern, prior to Omicron subvariant adapted boostering. Multiple booster vaccine doses can provide effective protection from COVID-19, even with intensive anti-CD38 therapy for high-risk MM.
dc.formatPrint-Electronic
dc.format.extent845 - 850
dc.languageeng
dc.language.isoeng
dc.publisherWILEY
dc.relation.ispartofBritish Journal of Haematology
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectanti-CD38
dc.subjectantibodies
dc.subjecthigh-dose therapy
dc.subjectmultiple myeloma
dc.subjectsevere acute respiratory syndrome coronavirus-2 (SARS-CoV-2)
dc.subjectHumans
dc.subjectCOVID-19
dc.subjectSARS-CoV-2
dc.subjectMultiple Myeloma
dc.subjectVaccination
dc.subjectImmunity
dc.subjectUnited Kingdom
dc.subjectAntibodies, Viral
dc.titleImmune responses to COVID-19 booster vaccinations in intensively anti-CD38 antibody treated patients with ultra-high-risk multiple myeloma: results from the Myeloma UK (MUK) nine OPTIMUM trial.
dc.typeJournal Article
dcterms.dateAccepted2023-02-14
dc.date.updated2023-06-02T10:27:32Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1111/bjh.18714
rioxxterms.licenseref.startdate2023-06-01
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/36895158
pubs.issue5
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Myeloma Molecular Therapy
pubs.publication-statusPublished
pubs.publisher-urlhttp://dx.doi.org/10.1111/bjh.18714
pubs.volume201
icr.researchteamMyeloma Molecular Therapy
dc.contributor.icrauthorKaiser, Martin
icr.provenanceDeposited by Mr Arek Surman on 2023-06-02. Deposit type is initial. No. of files: 1. Files: Br J Haematol - 2023 - Faustini - Immune responses to COVID‐19 booster vaccinations in intensively anti‐CD38 antibody.pdf


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