Evidence map›Paper›PMID 41466249›Full record

Observational studyBMC medicine2025

Hybrid, infection- and vaccination-induced protection against laboratory- confirmed SARS-CoV-2 infection in a European multi-centre prospective cohort of healthcare workers, 2021-2024.

Madelyn Rojas-Castro, Ranya Mulchandani, Kim Brolin, Zvjezdana Lovrić Makarić, Anneli Uusküla, Colm Bergin, Catherine Fleming, Paolo Bonfanti, Rita Murri, Viesturs Zvirbulis and 36 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in BMC medicine, 2025. 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

46 authors.

Madelyn Rojas-CastroDepartment of Epidemiology, Epiconcept, Paris, France. m.rojas@epiconcept.fr.ORCID 0000-0001-7006-7946
Ranya MulchandaniDepartment of Epidemiology, Epiconcept, Paris, France.ORCID 0000-0002-5157-1060
Kim BrolinEuropean Centre for Disease Prevention and Control, Stockholm, Sweden.ORCID 0009-0000-4353-7922
Zvjezdana Lovrić MakarićCroatian Institute of Public Health, Zagreb, Croatia.ORCID 0000-0003-4285-2116
Anneli UuskülaInstitute of Family Medicine and Public Health, University of Tartu, Tartu, Estonia.ORCID 0000-0002-4036-3856
Colm BerginDepartment of Genitourinary Medicine and Infectious Diseases (GUIDe), St. James's Hospital, Dublin, Ireland.
Catherine FlemingDepartment of Infectious Diseases, University Hospital Galway, Galway, Ireland.
Paolo BonfantiInfectious Diseases Unit, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.ORCID 0000-0001-7289-8823
Rita MurriUniversità Cattolica del Sacro Cuore, Rome, Italy.ORCID 0000-0001-9468-5458
Viesturs ZvirbulisPauls Stradins University Hospital, Riga, Latvia.
Dace ZavadskaChildren Clinical University Hospital, Riga, Latvia.ORCID 0000-0003-4892-3763
Konstanty SzuldrzynskiNational Medical Institute of the Ministry of the Interior and Administration, Warsaw, Poland.
Vânia GaioDepartment of Epidemiology, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.
Corneliu Petru PopescuDr Victor Babes Clinical Hospital of Infectious and Tropical Diseases, Bucharest, Romania.
Mihai CraiuFaculty of Medicine, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Raluca-Maria HrișcăCentral Military Emergency University Hospital Dr Carol Davila, Bucharest, Romania.
Maria CisnerosInstitut de Recerca Sant Joan de Deu. Hospital Sant Joan de Deu, Barcelona, Spain.
Miriam Latorre-MillánResearch Group on Difficult to Diagnose and Treat Infections, Miguel Servet University Hospital (IIS Aragón), Zaragoza, Spain.ORCID 0000-0001-9932-0124
Goranka PetrovićCroatian Institute of Public Health, Zagreb, Croatia.ORCID 0000-0001-8304-5519
Liss LohurOutpatient Department, Viljandi Hospital, Viljandi, Estonia.
Jonathan McGrathDepartment of Genitourinary Medicine and Infectious Diseases (GUIDe), St. James's Hospital, Dublin, Ireland.
Lauren FergusonDepartment of Infectious Diseases, University Hospital Galway, Galway, Ireland.
Anna SpoltiInfectious Diseases Unit, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.
Katleen De Gaetano DonatiUniversità Cattolica del Sacro Cuore, Rome, Italy.
Ilze AbolinaPauls Stradins University Hospital, Riga, Latvia.
Dagne GraveleChildren Clinical University Hospital, Riga, Latvia.
Ausenda MachadoDepartment of Epidemiology, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.ORCID 0000-0002-1849-1499
Simin Aysel FlorescuDr Victor Babes Clinical Hospital of Infectious and Tropical Diseases, Bucharest, Romania.
Mihaela LazarCantacuzino National Military-Medical Institute for Research and Development, Bucharest, Romania.ORCID 0000-0002-8226-6026
Pilar SubiratsInstitut de Recerca Sant Joan de Deu. Hospital Sant Joan de Deu, Barcelona, Spain.
Laura ClusaResearch Group on Difficult to Diagnose and Treat Infections, Miguel Servet University Hospital (IIS Aragón), Zaragoza, Spain.ORCID 0000-0002-3503-2331
Gordan SarajlićCroatian Institute of Public Health, Zagreb, Croatia.ORCID 0009-0000-3722-8795
Jacklyn SuiDepartment of Genitourinary Medicine and Infectious Diseases (GUIDe), St. James's Hospital, Dublin, Ireland.
Claire KennyDepartment of Medicine, University of Galway, Dublin, Ireland.
Rosaria SantangeloUniversità Cattolica del Sacro Cuore, Rome, Italy.
Dainis KrievinsPauls Stradins University Hospital, Riga, Latvia.
Elza Anna BarzdinaChildren Clinical University Hospital, Riga, Latvia.
Camila Valadas HenriquesDepartment of Infectious Diseases, National Institute of Health Doutor Ricardo Jorge, Lisbon, Portugal.
Alma Gabriela KosaDr Victor Babes Clinical Hospital of Infectious and Tropical Diseases, Bucharest, Romania.
Săftica-Mariana PohribCentral Military Emergency University Hospital Dr Carol Davila, Bucharest, Romania.
Victor Daniel MironFaculty of Medicine, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Carmen Muñoz-AlmagroInstitut de Recerca Sant Joan de Deu. Hospital Sant Joan de Deu, Barcelona, Spain.ORCID 0000-0001-5586-404X
Ana Maria MilagroResearch Group on Difficult to Diagnose and Treat Infections, Miguel Servet University Hospital (IIS Aragón), Zaragoza, Spain.ORCID 0000-0002-3888-8952
Sabrina BacciEuropean Centre for Disease Prevention and Control, Stockholm, Sweden.
Camelia SavulescuDepartment of Epidemiology, Epiconcept, Paris, France. c.savulescu@epiconcept.fr.ORCID 0000-0002-5374-835X
VEBIS HCW VE study group

Funding

European Centre for Disease Prevention and Control ECDC/2021/017
6 · The paper itself

Abstract

backgroundHealthcare workers (HCWs) face high occupational exposure to SARS-CoV-2 and are a priority group for vaccination. Both natural infection and vaccination-individually or combined as hybrid immunity-confer protection against SARS-CoV-2 infection. This study aimed to evaluate the protection conferred by hybrid, infection-induced, and booster vaccine-induced immunity against laboratory-confirmed SARS-CoV-2 infections in HCWs during the circulation of three pandemic and one post-pandemic Omicron sublineages.

methodsWe conducted a prospective cohort study of HCWs from 18 hospitals across nine European countries. Participants underwent RT-PCR testing at enrolment and during weekly or fortnightly follow-ups. The study period was divided based on dominant Omicron sublineage circulation: BA.1/2 (Dec 16, 2021-Jun 1, 2022), BA.4/5/BQ.1 (Jun 2-Dec 31, 2022), BA.2/XBB (Jan 1-May 2, 2023), and post-pandemic XBB.1.5/BA.2.86 (Sep 1, 2023-May 21, 2024). Participants were classified into four groups: hybrid (prior infection and recent booster vaccination 7-179 days), infection-induced (prior infection, no recent vaccination), vaccine-induced immunity (recent booster vaccination, no prior infection), and a reference group (no prior infection, no recent booster vaccination). Adjusted hazard ratios (aHRs) for infection were estimated using Cox regression, adjusting for hospital, age, sex, chronic condition, and patient-facing role.

resultsA total of 3 133 HCWs were included: 2572 (82%) female, 1734 (55%) aged 40-59, and 563 (29%) with ≥ 1 chronic condition. Hybrid immunity showed significant protection during BA.1/2 (aHR = 0.37, 95%CI 0.21-0.63), BA.4/5/BQ.1 (aHR = 0.36, 95%CI 0.22-0.58), and XBB.1.5/BA.2.86 (aHR = 0.53, 95%CI 0.37-0.74) periods. Infection-induced immunity was protective across all periods, most during BA.1/2 (aHR = 0.26, 95%CI 0.12-0.53), and least during BA.2/XBB (aHR = 0.66, 95%CI 0.36-1.22). Vaccine-induced immunity alone offered limited protection during BA.1/2 (aHR = 0.72, 95%CI 0.49-1.06) and BA.4/5/BQ.1 (aHR = 0.77, 95%CI 0.50-1.19), with wide confidence intervals suggesting low statistical significance.

conclusionsHybrid and infection-induced immunity groups were more protected against infection caused by earlier Omicron sub-lineages and more protected than vaccination alone, which had no significant protective effect. These findings highlight the need for adaptive public health strategies, including timely vaccine updates and understanding of prior SARS-CoV-2 infection to inform COVID-19 vaccination policies for HCWs in the post-pandemic era.

Indexed as

COVID-19COVID-19 VaccinesHealth PersonnelSARS-CoV-2AdultEuropeFemaleHumansImmunization, SecondaryMaleMiddle AgedProspective StudiesVaccinationCOVID-19 VaccinesCOVID-19 vaccinationHealthcare workersHybrid immunityOmicron variantProspective cohort study

Identifiers

PMID41466249
PMCPMC12751633

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LicenceCC BY-NC-ND
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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.