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10.1038/s41467-021-27544-6

http://scihub22266oqcxt.onion/10.1038/s41467-021-27544-6
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suck abstract from ncbi


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pmid34893640      Nat+Commun 2021 ; 12 (1): 7222
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  • Proteomic profiling of MIS-C patients indicates heterogeneity relating to interferon gamma dysregulation and vascular endothelial dysfunction #MMPMID34893640
  • Diorio C; Shraim R; Vella LA; Giles JR; Baxter AE; Oldridge DA; Canna SW; Henrickson SE; McNerney KO; Balamuth F; Burudpakdee C; Lee J; Leng T; Farrel A; Lambert MP; Sullivan KE; Wherry EJ; Teachey DT; Bassiri H; Behrens EM
  • Nat Commun 2021[Dec]; 12 (1): 7222 PMID34893640show ga
  • Multi-system Inflammatory Syndrome in Children (MIS-C) is a major complication of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection in pediatric patients. Weeks after an often mild or asymptomatic initial infection with SARS-CoV-2 children may present with a severe shock-like picture and marked inflammation. Children with MIS-C present with varying degrees of cardiovascular and hyperinflammatory symptoms. Here we perform a comprehensive analysis of the plasma proteome of more than 1400 proteins in children with SARS-CoV-2. We hypothesize that the proteome would reflect heterogeneity in hyperinflammation and vascular injury, and further identify pathogenic mediators of disease. We show that protein signatures demonstrate overlap between MIS-C, and the inflammatory syndromes macrophage activation syndrome (MAS) and thrombotic microangiopathy (TMA). We demonstrate that PLA2G2A is an important marker of MIS-C that associates with TMA. We find that IFNgamma responses are dysregulated in MIS-C patients, and that IFNgamma levels delineate clinical heterogeneity.
  • |*Proteome[MESH]
  • |Biomarkers[MESH]
  • |COVID-19/*complications/metabolism/pathology[MESH]
  • |Case-Control Studies[MESH]
  • |Chemokine CXCL9[MESH]
  • |Child[MESH]
  • |Endothelium, Vascular/*physiopathology[MESH]
  • |Group II Phospholipases A2[MESH]
  • |Humans[MESH]
  • |Inflammation[MESH]
  • |Interferon-gamma/*immunology[MESH]
  • |Interleukin-10[MESH]
  • |Proteomics[MESH]
  • |Systemic Inflammatory Response Syndrome/metabolism/*pathology[MESH]


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