Evidence map›Paper›PMID 39835131›Full record

ArticleFrontiers in immunology2024

Distinct response patterns of endothelial markers to the BNT162b2 mRNA COVID-19 booster vaccine are associated with the spike-specific IgG antibody production.

Beatriz Castro-Robles, Francisco J Cimas, Lourdes Arias-Salazar, Jesús Ontañón, Julia Lozano, Susana López-López, Fernando Andrés-Pretel, María Ángeles Requena-Calleja, Antonio Mas, Gemma Serrano-Heras and 2 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

12 authors.

Beatriz Castro-RoblesResearch Unit, General University Hospital of Albacete, Health Service of Castilla-La Mancha (SESCAM), Albacete, Spain.
Francisco J CimasMolecular Oncology Laboratory, Molecular Medicine Unit, Associated Unit of Biomedicine, University of Castilla-La Mancha-Spanish National Research Council (UCLM-CSIC), Albacete, Spain.
Lourdes Arias-SalazarResearch Unit, General University Hospital of Albacete, Health Service of Castilla-La Mancha (SESCAM), Albacete, Spain.
Jesús OntañónImmunology Unit, Clinical Analysis Department, General University Hospital of Albacete, Albacete, Spain.
Julia LozanoMicrobiology Department, General University Hospital of Albacete, Albacete, Spain.
Susana López-LópezResearch Unit, General University Hospital of Albacete, Health Service of Castilla-La Mancha (SESCAM), Albacete, Spain.
Fernando Andrés-PretelResearch Unit, General University Hospital of Albacete, Department of Statistics, Foundation of the National Paraplegics Hospital of Toledo, Albacete, Spain.
María Ángeles Requena-CallejaInternal Medicine Department, General University Hospital of Albacete, Albacete, Spain.
Antonio MasBiomedicine Institute of UCLM (IB-UCLM), Faculty of Medicine, University of Castilla-La Mancha, Albacete, Spain.
Gemma Serrano-HerasResearch Unit, General University Hospital of Albacete, Health Service of Castilla-La Mancha (SESCAM), Albacete, Spain.
Tomás SeguraBiomedicine Institute of UCLM (IB-UCLM), Faculty of Medicine, University of Castilla-La Mancha, Albacete, Spain.
Javier SoleraFaculty of Medicine, University of Castilla-La Mancha, Albacete, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Despite the efficacy and safety of SARS-CoV-2 vaccines, inflammatory and/or thrombotic episodes have been reported. Since the impact of COVID-19 vaccines on the endothelium remains uncertain, our objective was to assess endothelial activation status before and 90 days after the third dose of the BNT162b2 mRNA COVID-19 vaccine. Methods: A prospective longitudinal study was conducted at University General Hospital of Albacete, involving 38 healthy health-care workers. Serum levels of endothelial markers (endocan and sVCAM-1) and spike S1-specific IgG antibodies were determined before and at 7, 15, 24 and 90days following vaccination. To analyze each participant´s individual response, we calculated relative increases/decreases (delta values) in endothelial markers and antibodies concentrations compared to their pre-vaccination levels. Results: We identified two significantly distinct profiles of endothelial markers response, characterized by either increased or decreased serum levels of endocan and sVCAM. Incremental and decremental response groups did not differ in terms of age, sex, cardiovascular risk factors, previous SARS-CoV-2 infection and influenza vaccine co-administration. However, these responses were significantly associated with the relative spike-specific antibody production. Specifically, the greatest relative increase in antibodies was found in the decremental responders. Additionally, the higher delta antibody production was observed in non-previously infected individuals. Conclusion: Administration of the BNT162b2 booster vaccine triggered a non-homogenous response of endothelial function markers among the study participants. Our findings improve the understanding of individual responses to the mRNA COVID-19 booster vaccine, which could be useful in assessing the need for booster doses, particularly in population at risk of vascular complications.

Indexed as

Antibodies, ViralBNT162 VaccineCOVID-19COVID-19 VaccinesImmunoglobulin GSARS-CoV-2Spike Glycoprotein, CoronavirusAdultBiomarkersFemaleHumansImmunization, SecondaryLongitudinal StudiesMaleMiddle AgedProspective StudiesAntibodies, ViralBiomarkersBNT162 VaccineCOVID-19 VaccinesImmunoglobulin GSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Vascular Cell Adhesion Molecule-1anti-spike antibodiesbooster doseendocanendothelial dysfunctionIgGmRNA COVID-19 vaccinesSARS-CoV-2VCAM-1

Identifiers

PMID39835131
PMCPMC11743620

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.