Rapid seroconversion and persistent functional IgG antibodies in severe COVID-19 patients correlates with an IL-12p70 and IL-33 signature

Despite ongoing efforts to characterize the host response toward SARS-CoV-2, a major gap in our knowledge still exists regarding the magnitude and duration of the humoral response. Analysis of the antibody response in mild versus moderate/severe patients, using our new developed quantitative electro...

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Veröffentlicht in:Scientific reports 2021-02, Vol.11 (1), p.3461-3461, Article 3461
Hauptverfasser: Munitz, Ariel, Edry-Botzer, L., Itan, M., Tur-Kaspa, R., Dicker, D., Marcoviciu, D., Goren, M. G., Mor, M., Lev, S., Gottesman, T., Muhsen, K., Cohen, D., Stein, M., Qimron, U., Freund, N. T., Wine, Y., Gerlic, Motti
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Sprache:eng
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Zusammenfassung:Despite ongoing efforts to characterize the host response toward SARS-CoV-2, a major gap in our knowledge still exists regarding the magnitude and duration of the humoral response. Analysis of the antibody response in mild versus moderate/severe patients, using our new developed quantitative electrochemiluminescent assay for detecting IgM/IgA/IgG antibodies toward SARS-CoV-2 antigens, revealed a rapid onset of IgG/IgA antibodies, specifically in moderate/severe patients. IgM antibodies against the viral receptor binding domain, but not against nucleocapsid protein, were detected at early stages of the disease. Furthermore, we observed a marked reduction in IgM/IgA antibodies over-time. Adapting our assay for ACE2 binding-competition, demonstrated that the presence of potentially neutralizing antibodies is corelated with IgG/IgA. Finally, analysis of the cytokine profile in COVID-19 patients revealed unique correlation of an IL-12p70/IL33 and IgG seroconversion, which correlated with disease severity. In summary, our comprehensive analysis has major implications on the understanding and monitoring of SARS-CoV-2 infections.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-021-83019-0