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10.1371/journal.ppat.1009243

http://scihub22266oqcxt.onion/10.1371/journal.ppat.1009243
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33524041!7877736!33524041
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suck abstract from ncbi


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pmid33524041      PLoS+Pathog 2021 ; 17 (2): e1009243
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  • Metabolomic/lipidomic profiling of COVID-19 and individual response to tocilizumab #MMPMID33524041
  • Meoni G; Ghini V; Maggi L; Vignoli A; Mazzoni A; Salvati L; Capone M; Vanni A; Tenori L; Fontanari P; Lavorini F; Peris A; Bartoloni A; Liotta F; Cosmi L; Luchinat C; Annunziato F; Turano P
  • PLoS Pathog 2021[Feb]; 17 (2): e1009243 PMID33524041show ga
  • The current pandemic emergence of novel coronavirus disease (COVID-19) poses a relevant threat to global health. SARS-CoV-2 infection is characterized by a wide range of clinical manifestations, ranging from absence of symptoms to severe forms that need intensive care treatment. Here, plasma-EDTA samples of 30 patients compared with age- and sex-matched controls were analyzed via untargeted nuclear magnetic resonance (NMR)-based metabolomics and lipidomics. With the same approach, the effect of tocilizumab administration was evaluated in a subset of patients. Despite the heterogeneity of the clinical symptoms, COVID-19 patients are characterized by common plasma metabolomic and lipidomic signatures (91.7% and 87.5% accuracy, respectively, when compared to controls). Tocilizumab treatment resulted in at least partial reversion of the metabolic alterations due to SARS-CoV-2 infection. In conclusion, NMR-based metabolomic and lipidomic profiling provides novel insights into the pathophysiological mechanism of human response to SARS-CoV-2 infection and to monitor treatment outcomes.
  • |*COVID-19 Drug Treatment[MESH]
  • |*Lipidomics[MESH]
  • |Antibodies, Monoclonal, Humanized/*administration & dosage[MESH]
  • |COVID-19/blood/epidemiology[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Lipids/*blood[MESH]
  • |Male[MESH]
  • |Nuclear Magnetic Resonance, Biomolecular[MESH]


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