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10.1172/JCI144554

http://scihub22266oqcxt.onion/10.1172/JCI144554
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33497356!7954607!33497356
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suck abstract from ncbi


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pmid33497356      J+Clin+Invest 2021 ; 131 (6): ä
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  • Similarities and differences between the immunopathogenesis of COVID-19-related pediatric multisystem inflammatory syndrome and Kawasaki disease #MMPMID33497356
  • Esteve-Sole A; Anton J; Pino-Ramirez RM; Sanchez-Manubens J; Fumado V; Fortuny C; Rios-Barnes M; Sanchez-de-Toledo J; Girona-Alarcon M; Mosquera JM; Ricart S; Launes C; de Sevilla MF; Jou C; Munoz-Almagro C; Gonzalez-Roca E; Vergara A; Carrillo J; Juan M; Cuadras D; Noguera-Julian A; Jordan I; Alsina L
  • J Clin Invest 2021[Mar]; 131 (6): ä PMID33497356show ga
  • Multisystem inflammatory syndrome associated with the SARS-CoV-2 pandemic has recently been described in children (MIS-C), partially overlapping with Kawasaki disease (KD). We hypothesized that (a) MIS-C and prepandemic KD cytokine profiles may be unique and justify the clinical differences observed, and (b) SARS-CoV-2-specific immune complexes (ICs) may explain the immunopathology of MIS-C. Seventy-four children were included: 14 with MIS-C, 9 patients positive for SARS-CoV-2 by PCR without MIS-C (COVID), 14 with prepandemic KD, and 37 healthy controls (HCs). Thirty-four circulating cytokines were quantified in pretreatment serum or plasma samples and the presence of circulating SARS-CoV-2 ICs was evaluated in MIS-C patients. Compared with HCs, the MIS-C and KD groups showed most cytokines to be significantly elevated, with IFN-gamma-induced response markers (including IFN-gamma, IL-18, and IP-10) and inflammatory monocyte activation markers (including MCP-1, IL-1alpha, and IL-1RA) being the main triggers of inflammation. In linear discriminant analysis, MIS-C and KD profiles overlapped; however, a subgroup of MIS-C patients (MIS-Cplus) differentiated from the remaining MIS-C patients in IFN-gamma, IL-18, GM-CSF, RANTES, IP-10, IL-1alpha, and SDF-1 and incipient signs of macrophage activation syndrome. Circulating SARS-CoV-2 ICs were not detected in MIS-C patients. Our findings suggest a major role for IFN-gamma in the pathogenesis of MIS-C, which may be relevant for therapeutic management.
  • |Adolescent[MESH]
  • |Antibodies, Viral/blood[MESH]
  • |Antigen-Antibody Complex/blood[MESH]
  • |Antigens, Viral/blood[MESH]
  • |COVID-19/*etiology/immunology/virology[MESH]
  • |Case-Control Studies[MESH]
  • |Child[MESH]
  • |Child, Preschool[MESH]
  • |Cohort Studies[MESH]
  • |Cross-Sectional Studies[MESH]
  • |Cytokines/*blood[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Infant[MESH]
  • |Interferon-gamma/blood[MESH]
  • |Male[MESH]
  • |Models, Immunological[MESH]
  • |Mucocutaneous Lymph Node Syndrome/*etiology/immunology[MESH]
  • |Pandemics[MESH]
  • |SARS-CoV-2/genetics/immunology[MESH]


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