Show simple item record

 
dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorNguyen, Jennifer
dc.contributor.authorMitratza, Marianna
dc.contributor.authorVolkman, Hannah R
dc.contributor.authorde Munter, Leonie
dc.contributor.authorTran, Thao Mai Phuong
dc.contributor.authorMarques, Cátia
dc.contributor.authorOtero-Romero, Susana
dc.contributor.authorAntón Pagarolas, Andrés
dc.date.accessioned2025-03-12T07:59:37Z
dc.date.available2025-03-12T07:59:37Z
dc.date.copyright2024
dc.date.issued2025-01
dc.identifier.citationNguyen JL, Mitratza M, Volkman HR, de Munter L, Tran TMP, Marques C, et al. Effectiveness of the BNT162b2 XBB.1.5-adapted vaccine against COVID-19 hospitalization related to the JN.1 variant in Europe: a test-negative case-control study using the id.DRIVE platform. eClinicalMedicine. 2025 Jan;79:102995.
dc.identifier.issn2589-5370
dc.identifier.urihttp://hdl.handle.net/11351/12748
dc.descriptionCOVID-19 vaccination; SARS-CoV-2; Vaccine effectiveness
dc.description.abstractBackground Prior studies have reported lower effectiveness of XBB.1.5-adapted vaccines against hospitalization related to the Omicron JN.1 variant than the XBB variant. This study evaluated the effectiveness and durability of the BNT162b2 XBB.1.5-adapted vaccine against JN.1-related hospitalization during the 2023–2024 season in Europe. Methods A test-negative case–control study was carried out in adults (≥18 y) hospitalized between 2 October 2023 and 2 April 2024 with severe acute respiratory infection (SARI) within the id.DRIVE partnership. This study included nine sites across Belgium, Germany, Italy, and Spain. Cases had a laboratory-confirmed JN.1 infection or a positive SARS-CoV-2 test with symptom onset during JN.1 predominance; controls had a negative SARS-CoV-2 test and symptom onset during JN.1 predominance. The primary objective was to estimate BNT162b2 XBB.1.5-adapted vaccine effectiveness (VE) against COVID-19 hospitalization. One case was matched with up to four controls, according to symptom onset date and site. Multivariable analyses were adjusted for symptom onset date, age, sex, and number of chronic conditions. Findings Among 308 test-positive cases and 1117 test-negative controls, BNT162b2 XBB.1.5-adapted VE against hospitalization compared to no vaccination this season was 53.8% (95% CI 38.4–65.4) after a median of 63 days following vaccination. Protection was sustained through five months; VE was 52.2% (95% CI 41.3–61.1) 2 to <4 weeks after vaccination, 48.9% (95% CI 17.9–68.2) at 4 to <8 weeks, and ranged from 54.6% to 59.5% at 4-week intervals from 8 to <22 weeks. Interpretation BNT162b2 XBB.1.5-adapted vaccine provided protection against JN.1-related hospitalization, regardless of prior vaccination history, with no evidence of waning through five months. These data support yearly vaccination against COVID-19 to prevent severe illness during the respiratory virus season.
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofserieseClinicalMedicine;79
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.sourceScientia
dc.subjectCOVID-19 (Malaltia) - Vacunació
dc.subjectAvaluació de resultats (Assistència sanitària)
dc.subjectHospitals - Ingressos i altes
dc.subject.meshCoronavirus Infections
dc.subject.mesh/prevention & control
dc.subject.meshVaccines
dc.subject.meshHospitalization
dc.subject.meshAntibodies, Viral
dc.subject.meshTreatment Outcome
dc.titleEffectiveness of the BNT162b2 XBB.1.5-adapted vaccine against COVID-19 hospitalization related to the JN.1 variant in Europe: a test-negative case-control study using the id.DRIVE platform
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.eclinm.2024.102995
dc.subject.decsinfecciones por Coronavirus
dc.subject.decs/prevención & control
dc.subject.decsvacunas
dc.subject.decshospitalización
dc.subject.decsanticuerpos víricos
dc.subject.decsresultado del tratamiento
dc.relation.publishversionhttps://doi.org/10.1016/j.eclinm.2024.102995
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Nguyen JL, Volkman HR, Marques C] Pfizer Inc., New York, NY, United States. [Mitratza M, de Munter L, Tran TMP] P95 Epidemiology and Pharmacovigilance, Leuven, Belgium. [Antón A] Servei de Microbiologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. [Otero-Romero S] Servei de Medicina Preventiva i Epidemiologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. Servei de Neurologia-Neuroimmunologia, Centre d’Esclerosi Múltiple de Catalunya (CEMCAT), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain
dc.identifier.pmid39726669
dc.identifier.wos001434970100001
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record