Evidence map›Paper›PMID 42192017›Full record

ArticleMolecular and cellular pediatrics2026

Sex differences in the long-term tolerability of BNT162b2 in children and adolescents.

Jeanne Moor, Vivien Grieshaber, Nicole Toepfner, Sarah Holzwarth, Matthias B Moor, Karolina Kublickiene, Christoph Strumann, Cho-Ming Chao

Abstract read
In one paragraph

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

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Jeanne Moor *Chair for Gender Medicine, University of Zurich, Zurich, Switzerland.
Vivien Grieshaber *Faculty of Health, Witten/Herdecke University, Witten, Germany.
Nicole ToepfnerDepartment of Pediatrics, Faculty of Medicine and University Hospital Carl Gustav Carus, Dresden University of Technology, Dresden, Germany.
Sarah HolzwarthDepartment of Pediatrics, Faculty of Medicine and University Hospital Carl Gustav Carus, Dresden University of Technology, Dresden, Germany.
Matthias B MoorDepartment of Nephrology and Hypertension, Inselspital University Hospital Bern, Bern, Switzerland.
Karolina KublickieneCLINTEC Division of Renal Medicine, Karolinska Institutet, Stockholm, Sweden.
Christoph StrumannUniversity Medical Center Schleswig-Holstein, Campus Luebeck, Luebeck, Germany.
Cho-Ming ChaoCardio-Pulmonary Institute (CPI), Universities of Giessen and Marburg Lung Center (UGMLC), Member of the German Center for Lung Research (DZL), Justus Liebig University Giessen, Giessen, Germany. c.chao@vincenz.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSex differences exist not only in the efficacy but also in adverse event rates of many vaccines. Here we compared the sex differences in the tolerability of BNT162b2 in children younger than 18 years in Germany.

methodsA post-hoc analysis of retrospectively collected tolerability data, collected through an authentication-based survey of legal guardians of children vaccinated with BNT162b2 under the age of 18 years (CoVacU18-study). Primary outcome was the frequency of the four most common post-vaccination symptom categories (local, general, musculoskeletal symptoms, fever) reported after the 1st-4th doses. Data were analyzed according to sex in bivariate analyses and regression models adjusting for age, weight, and dosage. Interactions between sex and age group effects on post-vaccination symptoms were assessed. An active-comparator analysis was applied to compare post-vaccination symptoms after BNT162b2 versus non-SARS-CoV-2 vaccines.

resultsThree thousand two hundred twenty-eight participants (median age 5.7 years, male 49.6%). In logistic regression, female sex was associated with higher odds of local symptoms (OR = 1.28 [95% CI: 1.17-1.40], p < 0.05), general symptoms (OR = 1.27 [1.13-1.44], p < 0.05), and musculoskeletal symptoms (OR = 1.27 [1.03-1.56], p < 0.05). Interactions between sex and age groups existed for post-vaccination local symptoms. Following non-BNT162b2 childhood vaccinations, female sex was not associated with odds of any post-vaccination symptoms. No relevant interaction existed between vaccine types (BNT162b2 vs non-BNT162b2) and sex for the association with post-vaccination symptoms.

conclusionSex differences exist in post-vaccination symptoms after BNT162b2 administration in young children and adolescents. These are of importance for the conception of approval studies, for post-vaccination monitoring and for future vaccination strategies.

Indexed as

BNT162b2FemaleMRNA VaccineSex differencesSex-specificVaccine reaction

Identifiers

PMID42192017
PMCPMC13212794

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