Evidence map›Paper›PMID 42252746›Full record

ArticleHuman vaccines & immunotherapeutics2026

Retrospective cohort study of mRNA COVID-19 vaccine-associated enhanced disease in the Vaccine Safety Datalink, 2021-23.

Edward A Belongia, Burney A Kieke, Kayla E Hanson, David L McClure, Thomas G Boyce, Matthew F Daley, Malini B DeSilva, Laura P Hurley, Stephanie A Irving, Lisa A Jackson and 3 more

Abstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 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

13 authors.

Edward A BelongiaMarshfield Clinic Research Institute, Marshfield, USA.ORCID 0000-0001-7478-0415
Burney A KiekeMarshfield Clinic Research Institute, Marshfield, USA.ORCID 0000-0002-7430-0570
Kayla E HansonMarshfield Clinic Research Institute, Marshfield, USA.ORCID 0009-0004-5117-8279
David L McClureMarshfield Clinic Research Institute, Marshfield, USA.ORCID 0000-0001-8470-7190
Thomas G BoyceMarshfield Clinic Research Institute, Marshfield, USA.ORCID 0000-0002-9579-6982
Matthew F DaleyInstitute for Health Research, Kaiser Permanente Colorado, Denver, USA.ORCID 0000-0003-1309-4096
Malini B DeSilvaHealthPartners Institute, Bloomington, USA.ORCID 0000-0003-3705-1672
Laura P HurleyAmbulatory Care Services, Denver Health and Hospitals, Denver, USA.ORCID 0000-0003-4699-8497
Stephanie A IrvingKaiser Permanente Center for Health Research, Portland, USA.ORCID 0000-0001-7437-6797
Lisa A JacksonKaiser Permanente Washington Health Research Institute, Seattle, USA.ORCID 0000-0002-1785-0218
Jonathan DuffyImmunization Safety Office, Centers for Disease Control and Prevention, Atlanta, USA.ORCID 0000-0002-8060-0940
Michael M McNeilImmunization Safety Office, Centers for Disease Control and Prevention, Atlanta, USA.ORCID 0000-0003-0713-8312
Maria E SundaramMarshfield Clinic Research Institute, Marshfield, USA.ORCID 0000-0001-8056-3302

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vaccine-associated enhanced disease (VAED) was recognized as a theoretical risk when COVID-19 vaccines were authorized. Epidemiologic data can identify a signal for VAED if vaccine effectiveness (VE) is negative for preventing serious illness. In 2021, we initiated a cohort study to examine VAED indirectly by estimating VE against COVID-19 hospitalization and severe illness in the Vaccine Safety Datalink. The study cohort included VSD enrollees who were age-eligible to receive mRNA COVID-19 vaccine from February 2021-March 2023. Outcomes were initial COVID-19-associated hospital admission and severe in-hospital complications (acute respiratory distress or failure). VE was estimated by dose, variant period, and for early (14-119 d) and late (≥120 d) post-vaccination periods. VE was defined as 100*(1- adjusted hazard ratio). Relative VE (rVE) was estimated for bivalent vaccine versus ≥2 monovalent vaccine doses. The hospitalization analysis included all 16,027 enrollees with COVID-19 hospitalization and a 5% random sample of non-hospitalized enrollees who contributed person-time (n = 138,238). Two-dose original monovalent VE against hospitalization exceeded 90% in most age groups during the pre-Delta and Delta periods. VE was lower during the Omicron period. During the Omicron BA.2/BA.4/BA.5/XBB period, a fourth monovalent dose or bivalent dose generated VE of 59%-78% across age groups with modest waning. rVE was 48%-60% across age groups for bivalent vaccine vs. ≥2 original monovalent doses. Overall, the results were similar for VE against severe in-hospital complication. In conclusion, there was no signal for VAED during any variant period or for any specific dose of monovalent or bivalent vaccine.

Indexed as

COVID-19COVID-19 VaccinesVaccine EfficacyAdolescentAdultAgedBNT162 VaccineChildChild, PreschoolFemaleHospitalizationHumansInfantMaleMiddle AgedRetrospective StudiesBNT162 VaccineCOVID-19 VaccinesVaccines, Syntheticantibody dependent enhancementCOVID-19hospitalizationseverityvaccine effectiveness

Identifiers

PMID42252746
PMCPMC13248906

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LicenceCC BY-NC
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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.