National Research Center for Hematology
Moscow, 125167, Russia
NCT Number: NCT05165719
Accuracy validation of the designed and manufactured ELISpot-based in vitro diagnostic 'Corona-T-test' for detection of SARS-CoV-2-specific T cells.
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Notify Me18 year and older
All sexes
Observational
Moscow, 125167, Russia
The investigators enrolled three independent cohorts of vaccinated (n = 69), convalescent (n = 50), and healthy but unvaccinated individuals (n = 101). Further, they estimated the T cell response to the designed peptide antigen panel, as measured by the manufactured ELISpot-based in vitro diagnostic 'Corona-T-test' to detect SARS-CoV-2-specific T cells.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Non-specific inclusion criteria
Healthy donors inclusion criteria
Convalescents inclusion criteria
Vaccinated inclusion criteria
Exclusion criteria
Corona-T-test - a single-color enzymatic ELISpot kit for the detection of interferon-gamma (IFNɣ), produced by the National Research Center for Hematology aiming detection of SARS-CoV-2-specific T cells
Time frame: 1 week
positive, negative, or inconclusive (gray-zone)
National Research Center for Hematology, Russia
Network
Validation of Specificity, Sensitivity, and Accuracy for an ELISpot-based In-vitro Diagnostic (IVD) Kit 'Corona-T-test' for Assessment of SARS-COV-2-specific T-cell Response
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