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Nucleocapsid Antibodies as an Optimal Serological Marker of SARS-CoV-2 Infection: A Longitudinal Study at the Thomayer University Hospital
M. Ibrahimová, V. Jamriková, K. Pavelková, K. Bořecká
Language English Country United States
Document type Journal Article
Grant support
Ministry of Health, Czech Republic: SARS-CoV-2-CZ-PREVAL-II
NU22-A-123
Ministerstvo zdravotnictví České republiky
TUH 00064190
Ministerstvo zdravotnictví České republiky
NLK
Directory of Open Access Journals
from 2019
PubMed Central
from 1997
Europe PubMed Central
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ProQuest Central
from 2019-03-01
Medline Complete (EBSCOhost)
from 2012-01-01
Health & Medicine (ProQuest)
from 2019-03-01
Public Health Database (ProQuest)
from 2019-03-01
Wiley-Blackwell Open Access Titles
from 2019
PubMed
39760288
DOI
10.1002/jcla.25149
Knihovny.cz E-resources
- MeSH
- Biomarkers blood MeSH
- COVID-19 * immunology blood diagnosis epidemiology MeSH
- Adult MeSH
- Phosphoproteins MeSH
- Spike Glycoprotein, Coronavirus immunology MeSH
- Interferon-gamma blood MeSH
- Coronavirus Nucleocapsid Proteins immunology MeSH
- Middle Aged MeSH
- Humans MeSH
- Longitudinal Studies MeSH
- Hospitals, University MeSH
- Nucleocapsid immunology MeSH
- Antibodies, Viral * blood MeSH
- SARS-CoV-2 * immunology MeSH
- COVID-19 Serological Testing methods MeSH
- Health Personnel * statistics & numerical data MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
BACKGROUND: The 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. METHODS: Blood 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). RESULTS: At 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. CONCLUSION: Nucleocapsid 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.
Department of Clinical Biochemistry Thomayer University Hospital Prague Czech Republic
Laboratory of Immunology Thomayer University Hospital Prague Czech Republic
References provided by Crossref.org
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