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10.1038/s41598-021-83019-0

http://scihub22266oqcxt.onion/10.1038/s41598-021-83019-0
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33568715!7876035!33568715
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suck abstract from ncbi


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pmid33568715      Sci+Rep 2021 ; 11 (1): 3461
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  • Rapid seroconversion and persistent functional IgG antibodies in severe COVID-19 patients correlates with an IL-12p70 and IL-33 signature #MMPMID33568715
  • Munitz A; Edry-Botzer L; Itan M; Tur-Kaspa R; Dicker D; Marcoviciu D; Goren MG; Mor M; Lev S; Gottesman T; Muhsen K; Cohen D; Stein M; Qimron U; Freund NT; Wine Y; Gerlic M
  • Sci Rep 2021[Feb]; 11 (1): 3461 PMID33568715show ga
  • 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.
  • |Antibody Formation[MESH]
  • |COVID-19/blood/diagnosis/*immunology[MESH]
  • |Humans[MESH]
  • |Immunoglobulin G/*immunology[MESH]
  • |Interleukin-12/*blood[MESH]
  • |Interleukin-33/*blood[MESH]
  • |Seroconversion/*physiology[MESH]


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