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Multisystem inflammatory syndrome in children and COVID-19 are distinct presentations of SARS-CoV-2.
Diorio, Caroline; Henrickson, Sarah E; Vella, Laura A; McNerney, Kevin O; Chase, Julie; Burudpakdee, Chakkapong; Lee, Jessica H; Jasen, Cristina; Balamuth, Fran; Barrett, David M; Banwell, Brenda L; Bernt, Kathrin M; Blatz, Allison M; Chiotos, Kathleen; Fisher, Brian T; Fitzgerald, Julie C; Gerber, Jeffrey S; Gollomp, Kandace; Gray, Christopher; Grupp, Stephan A; Harris, Rebecca M; Kilbaugh, Todd J; John, Audrey R Odom; Lambert, Michele; Liebling, Emily J; Paessler, Michele E; Petrosa, Whitney; Phillips, Charles; Reilly, Anne F; Romberg, Neil D; Seif, Alix; Sesok-Pizzini, Deborah A; Sullivan, Kathleen E; Vardaro, Julie; Behrens, Edward M; Teachey, David T; Bassiri, Hamid.
  • Diorio C; Immune Dysregulation Frontier Program.
  • Henrickson SE; Division of Oncology.
  • Vella LA; Immune Dysregulation Frontier Program.
  • McNerney KO; Division of Allergy and Immunology.
  • Chase J; Immune Dysregulation Frontier Program.
  • Burudpakdee C; Division of Infectious Diseases.
  • Lee JH; Immune Dysregulation Frontier Program.
  • Jasen C; Division of Oncology.
  • Balamuth F; Immune Dysregulation Frontier Program.
  • Barrett DM; Division of Rheumatology.
  • Banwell BL; Immune Dysregulation Frontier Program.
  • Bernt KM; Immune Dysregulation Frontier Program.
  • Blatz AM; Immune Dysregulation Frontier Program.
  • Chiotos K; Division of Allergy and Immunology.
  • Fisher BT; Division of Emergency Medicine, and.
  • Fitzgerald JC; Immune Dysregulation Frontier Program.
  • Gerber JS; Division of Oncology.
  • Gollomp K; Immune Dysregulation Frontier Program.
  • Gray C; Division of Neurology, Department of Pediatrics.
  • Grupp SA; Division of Oncology.
  • Harris RM; Division of Infectious Diseases.
  • Kilbaugh TJ; Division of Critical Care Medicine, Department of Anesthesiology and Critical Care Medicine, and.
  • John ARO; Immune Dysregulation Frontier Program.
  • Lambert M; Division of Infectious Diseases.
  • Liebling EJ; Division of Critical Care Medicine, Department of Anesthesiology and Critical Care Medicine, and.
  • Paessler ME; Division of Infectious Diseases.
  • Petrosa W; Immune Dysregulation Frontier Program.
  • Phillips C; Division of Hematology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Reilly AF; Immune Dysregulation Frontier Program.
  • Romberg ND; Division of Oncology.
  • Seif A; Division of Infectious Diseases.
  • Sesok-Pizzini DA; Division of Critical Care Medicine, Department of Anesthesiology and Critical Care Medicine, and.
  • Sullivan KE; Division of Infectious Diseases.
  • Vardaro J; Immune Dysregulation Frontier Program.
  • Behrens EM; Division of Hematology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Teachey DT; Division of Rheumatology.
  • Bassiri H; Immune Dysregulation Frontier Program.
J Clin Invest ; 130(11): 5967-5975, 2020 11 02.
Article in English | MEDLINE | ID: covidwho-690425
ABSTRACT
BACKGROUNDInitial reports from the severe acute respiratory coronavirus 2 (SARS-CoV-2) pandemic described children as being less susceptible to coronavirus disease 2019 (COVID-19) than adults. Subsequently, a severe and novel pediatric disorder termed multisystem inflammatory syndrome in children (MIS-C) emerged. We report on unique hematologic and immunologic parameters that distinguish between COVID-19 and MIS-C and provide insight into pathophysiology.METHODSWe prospectively enrolled hospitalized patients with evidence of SARS-CoV-2 infection and classified them as having MIS-C or COVID-19. Patients with COVID-19 were classified as having either minimal or severe disease. Cytokine profiles, viral cycle thresholds (Cts), blood smears, and soluble C5b-9 values were analyzed with clinical data.RESULTSTwenty patients were enrolled (9 severe COVID-19, 5 minimal COVID-19, and 6 MIS-C). Five cytokines (IFN-γ, IL-10, IL-6, IL-8, and TNF-α) contributed to the analysis. TNF-α and IL-10 discriminated between patients with MIS-C and severe COVID-19. The presence of burr cells on blood smears, as well as Cts, differentiated between patients with severe COVID-19 and those with MIS-C.CONCLUSIONPediatric patients with SARS-CoV-2 are at risk for critical illness with severe COVID-19 and MIS-C. Cytokine profiling and examination of peripheral blood smears may distinguish between patients with MIS-C and those with severe COVID-19.FUNDINGFinancial support for this project was provided by CHOP Frontiers Program Immune Dysregulation Team; National Institute of Allergy and Infectious Diseases; National Cancer Institute; the Leukemia and Lymphoma Society; Cookies for Kids Cancer; Alex's Lemonade Stand Foundation for Childhood Cancer; Children's Oncology Group; Stand UP 2 Cancer; Team Connor; the Kate Amato Foundations; Burroughs Wellcome Fund CAMS; the Clinical Immunology Society; the American Academy of Allergy, Asthma, and Immunology; and the Institute for Translational Medicine and Therapeutics.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Complement Membrane Attack Complex / Cytokines / Coronavirus Infections / Systemic Inflammatory Response Syndrome / Pandemics / Betacoronavirus Type of study: Cohort study / Observational study / Prognostic study Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: English Journal: J Clin Invest Year: 2020 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Complement Membrane Attack Complex / Cytokines / Coronavirus Infections / Systemic Inflammatory Response Syndrome / Pandemics / Betacoronavirus Type of study: Cohort study / Observational study / Prognostic study Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Language: English Journal: J Clin Invest Year: 2020 Document Type: Article