Publication date: Jan 06, 2025
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. 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). 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. 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.
Concepts | Keywords |
---|---|
June | COVID‐19 |
Pandemic | hybrid immunity |
Pcr | IGRA |
Vaccination | nucleocapsid antibodies |
SARS‐CoV‐2 | |
serological marker | |
spike antibodies |
Semantics
Type | Source | Name |
---|---|---|
disease | MESH | SARS-CoV-2 Infection |
pathway | REACTOME | SARS-CoV-2 Infection |
disease | IDO | blood |
disease | MESH | reinfection |
disease | MESH | infection |
pathway | REACTOME | Release |
disease | IDO | assay |
drug | DRUGBANK | Pentaerythritol tetranitrate |