Evidence map›Paper›PMID 39760288›Full record

ArticleJournal of clinical laboratory analysis2025

Nucleocapsid Antibodies as an Optimal Serological Marker of SARS-CoV-2 Infection: A Longitudinal Study at the Thomayer University Hospital.

Markéta Ibrahimová, Vladislava Jamriková, Kateřina Pavelková, Klára Bořecká

Abstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2025. 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. Article
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

4 authors.

Markéta IbrahimováLaboratory of Immunology, Thomayer University Hospital, Prague, Czech Republic.ORCID https://orcid.org/0009-0007-5971-4349
Vladislava JamrikováDepartment of Clinical Biochemistry, Thomayer University Hospital, Prague, Czech Republic.
Kateřina PavelkováDepartment of Hospital Epidemiology and Infection Control, Thomayer University Hospital, Prague, Czech Republic.
Klára BořeckáDepartment of Clinical Biochemistry, Thomayer University Hospital, Prague, Czech Republic.ORCID https://orcid.org/0000-0003-3394-3120

Funding

Ministerstvo zdravotnictví České republiky NU22-A-123Ministerstvo zdravotnictví České republiky TUH 00064190Ministry of Health, Czech Republic: SARS-CoV-2-CZ-PREVAL-II
6 · The paper itself

Abstract

backgroundThe longitudinal study was conducted over the initial 2 years of the COVID-19 pandemic, spanning from June 2020 to December 2022, in healthcare workers (HCWs) of the Thomayer University Hospital. A total of 3892 blood samples were collected and analyzed for total nucleocapsid (N) antibodies. The aim of the study was to evaluate the dynamics of N antibodies, their relationship to the PCR test, spike (S) antibodies, interferon-gamma, and prediction of reinfection with SARS-CoV-2.

methodsBlood collections were performed in three rounds, along with questionnaires addressing clinical symptoms of past infection, PCR testing, and vaccination. Antibody measurements included total N antibodies (Roche Diagnostics) and postvaccination S antibodies (Euroimmun). Cellular immunity was tested by interferon-gamma release assay (Euroimmun).

resultsAt the end of the study, 35.9% of HCWs were positive for N antibodies, and 39.5% of HCWs had either known PCR positivity or N antibodies or both. Ten percent of participants had no knowledge of a COVID-19 infection and 35% of positive individuals exhibited no symptoms. The values of positive antibodies decrease over a period of 6 months to 1 year, depending on the initial value, and their dynamics are highly variable. The study also demonstrated that the highest levels of spike antibodies and interferon-gamma occur during so-called hybrid immunity.

conclusionNucleocapsid antibodies proved valuable in monitoring SARS-CoV-2 infection dynamics, and they may detect cases of SARS-CoV-2 infection missed by PCR tests. The study identified distinct patterns in antibody dynamics and protection of hybrid immunity during reinfection.

Indexed as

Antibodies, ViralCoronavirus Nucleocapsid ProteinsCOVID-19COVID-19 Serological TestingNucleocapsidSARS-CoV-2AdultBiomarkersFemaleHealth PersonnelHospitals, UniversityHumansInterferon-gammaLongitudinal StudiesMaleMiddle AgedAntibodies, ViralBiomarkersCoronavirus Nucleocapsid ProteinsInterferon-gammanucleocapsid phosphoprotein, SARS-CoV-2PhosphoproteinsCOVID‐19hybrid immunityIGRAnucleocapsid antibodiesSARS‐CoV‐2serological markerspike antibodies

Identifiers

PMID39760288
PMCPMC11821721

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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.