Evidence map›Paper›PMID 40463399›Full record

ArticleBiomedical reports2025

Humoral immune response following the third dose of BNT162b2 received by employees at a Slovak cancer healthcare facility.

Patrik Palacka, Elena Marusakova, Katarina Rejlekova, Alena Svobodova, Lucia Skokanova, Martina Vulganova, Jana Obertova

Abstract read
In one paragraph

Article in Biomedical reports, 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
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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

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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

7 authors.

Patrik Palacka2nd Department of Oncology, Faculty of Medicine, Comenius University, 833 10 Bratislava, Slovakia.
Elena MarusakovaDepartment of Research and Development, Central-European Biotech Institute, 040 11 Kosice, Slovakia.
Katarina Rejlekova2nd Department of Oncology, Faculty of Medicine, Comenius University, 833 10 Bratislava, Slovakia.
Alena SvobodovaDepartment of Outpatient Chemotherapy, National Cancer Institute, 833 10 Bratislava, Slovakia.
Lucia SkokanovaDepartment of Outpatient Chemotherapy, National Cancer Institute, 833 10 Bratislava, Slovakia.
Martina VulganovaDepartment of Research and Development, Central-European Biotech Institute, 040 11 Kosice, Slovakia.
Jana Obertova2nd Department of Oncology, Faculty of Medicine, Comenius University, 833 10 Bratislava, Slovakia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BNT162b2 is a mRNA vaccine, approved by the US Food and Drug Administration and the European Medicines Agency that was designed to target Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), the causative agent of Coronavirus disease 2019 (COVID-19). Despite its widespread use, predictors of humoral immune responses after BNT162b2 administration remain uncertain. Consequently, a case-control study was conducted involving 273 employees at the National Cancer Institute (Bratislava, Slovakia) for the present study. Specifically, the present study aimed to determine the incidence of symptomatic COVID-19. In addition, the association between the safety of the third-dose BNT162b2 and sex and body mass index (BMI) was assessed. The present study also explored the potential determinants of plasma IgG antibody levels following vaccination. In total, 294 participants were recruited and 273 met the inclusion criteria. At a median follow-up of 4.7 months, 38 participants had symptomatic SARS-CoV-2 infection after vaccination. The incidence of adverse events (AEs) was found to be significantly higher in female patients compared with that in male patients. Furthermore, patients with a high BMI (≥30 kg/m²) had higher number of AEs compared with those with low BMI (P<0.05). IgG levels were observed to be significantly higher in male patients compared with those in female patients, in participants with high BMI compared with those with low BMI, in those experiencing three or more AEs compared with those with fewer AEs and in participants who had contracted COVID-19 compared with those who had not (P<0.05 for all). Multivariate analysis identified sex, BMI, number of AEs and prior COVID-19 infection as independent predictors of IgG plasma level (P<0.05). Therefore, the present study found the low number of COVID-19 in the subjects vaccinated with the third dose of BNT162b2 and revealed that the safety profile of the vaccine is associated with sex and BMI. Higher IgG levels, indicating more efficient protection against SARS-CoV-2, were observed in male patients, in participants with high BMI, those experiencing a higher frequency of AEs and those who had previously contracted COVID-19 despite vaccination against SARS-CoV-2. These findings could lead to the stratification of subjects within future clinical studies and the development of specific vaccination protocols in regard to sex, BMI and history of SARS-CoV-2.

Indexed as

BNT162b2IgG antibodiesinflammationsafetysymptomatic Coronavirus disease 2019

Identifiers

PMID40463399
PMCPMC12131294

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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.