FIELD: medical immunology.
SUBSTANCE: invention relates to the field of medical immunology and is intended to determine and quantify the specific cellular immunity to the antigens of the S-protein of the SARS-COV-2 virus. Mononuclear cells isolated from the patient's blood are incubated in the wells of a 96-well plate, at the bottom of which the full-size S-protein is sorbed as a test sample. On a flow cytofluorometer, the percentage of a subpopulation of double-positive T-lymphocytes CD8hiqhCD107a+ in the control and experimental samples is recorded. From the obtained value of the percentage of T-lymphocytes CD8hiqhCD107a in the test sample, the value of the percentage of T-lymphocytes CD8hiqhCD107a+ in the control sample is subtracted and the resulting difference in percentage is compared with the cut off value equal to 0.765%. If the obtained difference exceeds 0.765%, it is judged that the patient has specific cellular immunity to the antigens of the S-protein of the SARS-COV-2 virus in an amount equal to the obtained difference. If the obtained difference is less than 0.765%, it is judged that the patient has no specific cellular immunity.
EFFECT: invention makes it possible to quantitatively determine the cellular component of the immune defense against the SARS-COV-2 coronavirus both in those who have had COVID-19 and in vaccinated people.
1 cl, 1 dwg, 1 tbl, 1 ex
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Authors
Dates
2021-12-21—Published
2021-09-22—Filed