Evidence map›Paper›PMID 41671248›Full record

ArticlePloS one2026

Durability of the BNT162b2 XBB:1.5-adapted vaccine against JN.1 hospitalisation in Europe, October 2023 to August 2024: A test-negative case-control study using the id.DRIVE platform.

Hannah R Volkman, Leonie de Munter, Jennifer L Nguyen, Thao M P Tran, Marianna Mitratza, Cátia Marques, Laura Choi, Srinivas Valluri, Jingyan Yang, Andrés Antón and 14 more

Abstract readMulticenter Study
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Hannah R VolkmanPfizer Inc., New York, New York, United States of America.ORCID https://orcid.org/0000-0001-7274-9641
Leonie de MunterP95 Clinical and Epidemiology Services, Leuven, Belgium.ORCID https://orcid.org/0000-0001-6573-2032
Jennifer L NguyenPfizer Inc., New York, New York, United States of America.
Thao M P TranP95 Clinical and Epidemiology Services, Leuven, Belgium.ORCID https://orcid.org/0000-0003-2336-8302
Marianna MitratzaP95 Clinical and Epidemiology Services, Leuven, Belgium.
Cátia MarquesPfizer Inc., New York, New York, United States of America.
Laura ChoiPfizer Inc., New York, New York, United States of America.
Srinivas ValluriPfizer Inc., New York, New York, United States of America.
Jingyan YangPfizer Inc., New York, New York, United States of America.
Andrés AntónMicrobiology Department, Hospital Universitari Vall d'Hebron, Vall d'Hebron Institut de Recerca (VHIR), Universitat Autònoma de Barcelona, Barcelona, Spain.ORCID https://orcid.org/0000-0002-1476-0815
Irma CasasHospital Universitari Germans Trias i Pujol, Carretera del Canyet, Badalona, Barcelona, Spain.
Eduardo Conde-SousaP95 Clinical and Epidemiology Services, Leuven, Belgium.
Laura DrikiteP95 Clinical and Epidemiology Services, Leuven, Belgium.
Beate GrünerDepartment of Internal Medicine III, Division of Infectious Diseases, University Hospital Ulm, Ulm, Germany.ORCID https://orcid.org/0000-0001-6669-3741
Giancarlo IcardiCentro Interuniversitario per la Ricerca sull'Influenza e le altre Infezioni Trasmissibili - IRCCS Policlinico San Martino Hospital, Genoa, Italy.
Gerrit Luit Ten KateUniversitair Ziekenhuis Antwerpen, Edegem, Belgium.
Charlotte MartinLe Centre Hospitalier Universitaire St Pierre, Brussels, Belgium.
Ainara Mira-IglesiasVaccine Research Department, Fisabio - Public Health, Valencia, Spain.
Alejandro Orrico-SánchezVaccine Research Department, Fisabio - Public Health, Valencia, Spain.
Susana Otero-RomeroPreventive Medicine and Epidemiology Department, Hospital Universitari Vall d'Hebron, Vall d'Hebron Institut de Recerca (VHIR), Universitat Autònoma de Barcelona, Barcelona, Spain.
Gernot RohdeDepartment of Respiratory Medicine, Medical Clinic I, University Hospital, Goethe University Frankfurt, Frankfurt, Germany.
Luis JodarPfizer Inc., New York, New York, United States of America.
John M McLaughlinPfizer Inc., New York, New York, United States of America.
Kaatje BollaertsP95 Clinical and Epidemiology Services, Leuven, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhile multiple studies report that the BNT162b2 XBB.1.5-adapted mRNA COVID-19 vaccine (BNT162b2 XBB vaccine) is effective in preventing COVID-19 hospitalisation and death, effectiveness beyond six months remains unexplored.

methodsWe extended our previous study of BNT162b2 XBB vaccine effectiveness (VE) to evaluate durability against JN.1-related hospitalisation up to 46 weeks since dose using the id.DRIVE platform across Europe. This multi-country, multi-centre test-negative case-control study assessed the effectiveness and durability of the BNT162b2 XBB vaccine in preventing JN.1-associated hospitalisation among adults with severe acute respiratory infection between October 2023 and August 2024. Each case was matched with up to four controls by symptom onset date and study site. Multivariable analyses were adjusted for symptom onset date, age, sex, number of chronic conditions, and influenza vaccination receipt.

resultsAmong 827 test-positive cases and 2232 test-negative controls, protection against hospitalisation was sustained from two to <30 weeks since dose, with evidence of significant waning thereafter. VE was 64.5% (95% CI: 56.6; 71.0) at two to <30 weeks, and 4.9% (95% CI: -30.3; 30.7) at 30 to <46 weeks.

conclusionDespite the vaccine target not matching the predominant subvariant, BNT162b2 XBB vaccine protected against JN.1-related hospitalisation for up to 30 weeks. Protection against hospitalisation was non-significant after 30 weeks since dose, potentially due to further shift in circulating SARS-CoV-2 strains and/or waning immunity. Given the high COVID-19 activity in Europe during summer 2024, an additional vaccination after six months is warranted for those at risk of COVID-19 hospitalisation to maintain year-round protection.

Indexed as

COVID-19COVID-19 VaccinesHospitalizationSARS-CoV-2AdultAgedBNT162 VaccineCase-Control StudiesEuropeFemaleHumansMaleMiddle AgedVaccinationVaccine EfficacyBNT162 VaccineCOVID-19 Vaccines

Identifiers

PMID41671248
PMCPMC12893545

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.