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

Author:

Munitz ArielORCID,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 MottiORCID

Abstract

AbstractDespite 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.

Funder

Alpha-1 Foundation

United States-Israel Binational Science Foundation

Israel Science Foundation

Varda and Boaz Dotan Research Center for Hemato-Oncology Research, Tel Aviv University

development grant from Biological Industries, Beit Haemek, Israel

Israel Cancer Research Fund

H2020 European Research Council

Israeli Innovation Authority

Milner Foundation

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

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