Evidence map›Paper›PMID 41280926›Full record

ArticleFrontiers in immunology2025

Impact of immunodeficiencies on immunity induced by SARS-CoV-2 infection, mRNA BNT162b2 vaccination, and their combination in children and young adults.

Lubica Fialova, Birivan Macek-Nabova, Monika Zilkova, Natalia Turic-Csokova, Denisa Palova, Stanislav Katina, Gabriela Paulikova-Rolkova, Peter Ciznar, Julia Horakova, Lubica Wojciakova and 3 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 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

13 authors.

Lubica FialovaInstitute of Neuroimmunology, Slovak Academy of Sciences, Bratislava, Slovakia.
Birivan Macek-NabovaDepartment of Paediatric, National Institute of Children's Diseases, Bratislava, Slovakia.
Monika ZilkovaInstitute of Neuroimmunology, Slovak Academy of Sciences, Bratislava, Slovakia.
Natalia Turic-CsokovaInstitute of Neuroimmunology, Slovak Academy of Sciences, Bratislava, Slovakia.
Denisa PalovaInstitute of Neuroimmunology, Slovak Academy of Sciences, Bratislava, Slovakia.
Stanislav KatinaInstitute of Neuroimmunology, Slovak Academy of Sciences, Bratislava, Slovakia.
Gabriela Paulikova-RolkovaInstitute of Neuroimmunology, Slovak Academy of Sciences, Bratislava, Slovakia.
Peter CiznarDepartment of Paediatric, Medical Faculty Comenius University in Bratislava, Bratislava, Slovakia.
Julia HorakovaDepartment of Paediatric Haematology and Oncology, National Institute of Children's Diseases, Bratislava, Slovakia.
Lubica WojciakovaInstitute of Neuroimmunology, Slovak Academy of Sciences, Bratislava, Slovakia.
Karina MarkovaInstitute of Neuroimmunology, Slovak Academy of Sciences, Bratislava, Slovakia.
Eva KontsekovaInstitute of Neuroimmunology, Slovak Academy of Sciences, Bratislava, Slovakia.
Branislav KovacechInstitute of Neuroimmunology, Slovak Academy of Sciences, Bratislava, Slovakia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current understanding of how immunodeficiencies impact protective responses against viral infections and vaccination is primarily derived from adult cohorts that may not accurately reflect the pediatric, adolescent, and young adult population. This cross-sectional study aimed to evaluate immune responses in this underrepresented population affected by various immunodeficiencies after SARS-CoV-2 infection, two doses of the mRNA BNT162b2 vaccine, or after a combination of both. We analyzed blood samples from 102 immunocompromised patients (IC) (5-25 years) categorized into groups of primary immunodeficiencies (PID, n=17), bronchial asthma and allergic rhinitis (BA-AR, n=39), rheumatoid diseases (RD, n=21), and individuals who had undergone hematopoietic stem cell transplantation (HSCT, n=28), as well as 30 healthy individuals (9-26 years). We measured titres of Spike-specific IgM, IgA, and IgG antibody classes (including IgG subclasses) in plasma using ELISA and evaluated their inhibitory potential in a Spike-ACE2 cell-based internalization assay. Spike-specific CD4 T-cells were examined using a flow cytometry-based proliferation assay (FASCIA). In the IC group, all participants except eight generated detectable levels of IgG antibodies. The IgG titres induced by vaccination (Geometric mean titre (GMT

Indexed as

BNT162 VaccineCOVID-19COVID-19 VaccinesSARS-CoV-2AdolescentAdultAntibodies, ViralCD4-Positive T-LymphocytesChildChild, PreschoolCross-Sectional StudiesFemaleHumansImmunocompromised HostImmunoglobulin GMaleAntibodies, ViralBNT162 VaccineCOVID-19 VaccinesImmunoglobulin GSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2CD4 T-cellsGeometric mean titreinhibitory antibodiesmRNA BNT162b2 vaccineprimary and secondary immunodeficienciesSARS-CoV-2

Identifiers

PMID41280926
PMCPMC12634547

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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.