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10.1542/peds.2020-018242

http://scihub22266oqcxt.onion/10.1542/peds.2020-018242
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32879033!ä!32879033

suck abstract from ncbi


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pmid32879033      Pediatrics 2020 ; 146 (6): ä
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  • Quantitative SARS-CoV-2 Serology in Children With Multisystem Inflammatory Syndrome (MIS-C) #MMPMID32879033
  • Rostad CA; Chahroudi A; Mantus G; Lapp SA; Teherani M; Macoy L; Tarquinio KM; Basu RK; Kao C; Linam WM; Zimmerman MG; Shi PY; Menachery VD; Oster ME; Edupuganti S; Anderson EJ; Suthar MS; Wrammert J; Jaggi P
  • Pediatrics 2020[Dec]; 146 (6): ä PMID32879033show ga
  • OBJECTIVES: We aimed to measure severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) serological responses in children hospitalized with multisystem inflammatory syndrome in children (MIS-C) compared with those with coronavirus disease 2019 (COVID-19), those with Kawasaki disease (KD), and hospitalized pediatric controls. METHODS: From March 17, 2020, to May 26, 2020, we prospectively identified hospitalized children with MIS-C (n = 10), symptomatic COVID-19 (n = 10), and KD (n = 5) and hospitalized controls (n = 4) at Children's Healthcare of Atlanta. With institutional review board approval, we obtained prospective and residual blood samples from these children and measured SARS-CoV-2 spike receptor-binding domain (RBD) immunoglobulin M and immunoglobulin G (IgG), full-length spike IgG, and nucleocapsid protein antibodies using quantitative enzyme-linked immunosorbent assays and SARS-CoV-2 neutralizing antibodies using live-virus focus-reduction neutralization assays. We statistically compared the log-transformed antibody titers among groups and performed linear regression analyses. RESULTS: All children with MIS-C had high titers of SARS-CoV-2 RBD IgG antibodies, which correlated with full-length spike IgG antibodies (R (2) = 0.956; P < .001), nucleocapsid protein antibodies (R (2) = 0.846; P < .001), and neutralizing antibodies (R (2) = 0.667; P < .001). Children with MIS-C had significantly higher SARS-CoV-2 RBD IgG antibody titers (geometric mean titer 6800; 95% confidence interval 3495-13 231) than children with COVID-19 (geometric mean titer 626; 95% confidence interval 251-1563; P < .001), children with KD (geometric mean titer 124; 95% confidence interval 91-170; P < .001), and hospitalized controls (geometric mean titer 85; P < .001). All children with MIS-C also had detectable RBD immunoglobulin M antibodies, indicating recent SARS-CoV-2 infection. RBD IgG titers correlated with the erythrocyte sedimentation rate (R (2) = 0.512; P < .046) and with hospital (R (2) = 0.548; P = .014) and ICU lengths of stay (R (2) = 0.590; P = .010). CONCLUSIONS: Quantitative SARS-CoV-2 serology may have a role in establishing the diagnosis of MIS-C, distinguishing it from similar clinical entities, and stratifying risk for adverse outcomes.
  • |Adolescent[MESH]
  • |Antibodies, Neutralizing/blood[MESH]
  • |Antibodies, Viral/*blood[MESH]
  • |Blood Sedimentation[MESH]
  • |COVID-19 Serological Testing[MESH]
  • |COVID-19/blood/diagnosis/*immunology[MESH]
  • |Case-Control Studies[MESH]
  • |Child[MESH]
  • |Child, Preschool[MESH]
  • |Coronavirus Nucleocapsid Proteins/blood/*immunology[MESH]
  • |Diagnosis, Differential[MESH]
  • |Female[MESH]
  • |Hospitalization[MESH]
  • |Humans[MESH]
  • |Immunoglobulin G/blood[MESH]
  • |Immunoglobulin M/blood[MESH]
  • |Infant[MESH]
  • |Infant, Newborn[MESH]
  • |Length of Stay[MESH]
  • |Male[MESH]
  • |Mucocutaneous Lymph Node Syndrome/blood/diagnosis/*immunology[MESH]
  • |Neutralization Tests[MESH]
  • |Phosphoproteins/blood/immunology[MESH]
  • |Prospective Studies[MESH]
  • |Regression Analysis[MESH]
  • |SARS-CoV-2/*immunology[MESH]
  • |Spike Glycoprotein, Coronavirus/blood/*immunology[MESH]
  • |Systemic Inflammatory Response Syndrome/blood/diagnosis/*immunology[MESH]


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