Serologic and Cytokine Signatures in Children With Multisystem Inflammatory Syndrome and Coronavirus Disease 2019

Abstract Background The serologic and cytokine responses of children hospitalized with multisystem inflammatory syndrome (MIS-C) vs coronavirus disease 2019 (COVID-19) are poorly understood. Methods We performed a prospective, multicenter, cross-sectional study of hospitalized children who met the C...

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Veröffentlicht in:Open Forum Infectious Diseases 2022-03, Vol.9 (3), p.ofac070
Hauptverfasser: Lapp, Stacey A, Abrams, Joseph, Lu, Austin T, Hussaini, Laila, Kao, Carol M, Hunstad, David A, Rosenberg, Robert B, Zafferani, Marc J, Ede, Kaleo C, Ballan, Wassim, Laham, Federico R, Beltran, Yajira, Hsiao, Hui-Mien, Sherry, Whitney, Jenkins, Elan, Jones, Kaitlin, Horner, Anna, Brooks, Alyssa, Bryant, Bobbi, Meng, Lu, Hammett, Teresa A, Oster, Matthew E, Bamrah-Morris, Sapna, Godfred-Cato, Shana, Belay, Ermias, Chahroudi, Ann, Anderson, Evan J, Jaggi, Preeti, Rostad, Christina A
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Sprache:eng
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Zusammenfassung:Abstract Background The serologic and cytokine responses of children hospitalized with multisystem inflammatory syndrome (MIS-C) vs coronavirus disease 2019 (COVID-19) are poorly understood. Methods We performed a prospective, multicenter, cross-sectional study of hospitalized children who met the Centers for Disease Control and Prevention case definition for MIS-C (n = 118), acute COVID-19 (n = 88), or contemporaneous healthy controls (n = 24). We measured severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike receptor-binding domain (RBD) immunoglobulin G (IgG) titers and cytokine concentrations in patients and performed multivariable analysis to determine cytokine signatures associated with MIS-C. We also measured nucleocapsid IgG and convalescent RBD IgG in subsets of patients. Results Children with MIS-C had significantly higher SARS-CoV-2 RBD IgG than children with acute COVID-19 (median, 2783 vs 146; P 
ISSN:2328-8957
2328-8957
DOI:10.1093/ofid/ofac070