Current data in the literature demonstrate that the immune response to CoV-2-SARS is much more complex than initially assumed. In fact, beyond the humoral response, including the existence of neutralizing CAs, the adaptive lymphocyte T-type immune response also appears to play an important role in controlling the infection and reducing the severity of the disease. At this stage, the analysis of this T response is still rudimentary and underdeveloped, but it seems crucial to be able to analyze it effectively in COVID-19 patients, which could help predict the evolution of the infection. It is also currently difficult to know the evolution of this response over time and especially after the resolution of the infection. To this end, we will analyze the T lymphocyte response (ELISPOT and QUANTIFERON) based on the secretion of IFN (Th1) and IL-4 (Th2) by CoV-2-SARS specific T cells from COVID-19 patients. We will compare the T response to the quality of the systemic and mucosal humoral response. Finally, we will evaluate in parallel two new biomarkers of the severity of COVID-19: plasma calprotectin and the presence of antibodies to type 1 IFN antibodies.
Study Type
OBSERVATIONAL
Enrollment
73
measure of immune response by ELISPOT
measure of immune response by QUANTIFERON
CHU Saint-Etienne
Saint-Etienne, France
T cell immune response
Characterize T-cell immune response in patient with COVID 19 infection
Time frame: from baseline to 18 months
B cell immune response
Characterize B-cell immune response in patient with COVID 19 infection
Time frame: from baseline to 18 months
Platelet immune response
Characterize platelet immune response in patient with COVID 19 infection
Time frame: from baseline to 18 months
Immune response and chronic forms
Determine if there is a correlation between the pattern of immune response and the risk of reinfection or with persistence of symptoms in chronic forms of COVID-19.
Time frame: from baseline to 18 months
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