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10.1101/2021.02.09.430269

http://scihub22266oqcxt.onion/10.1101/2021.02.09.430269
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33594362!7885914!33594362
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suck abstract from ncbi


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pmid33594362      bioRxiv 2021 ; ä (ä): ä
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  • Integrated plasma proteomic and single-cell immune signaling network signatures demarcate mild, moderate, and severe COVID-19 #MMPMID33594362
  • Feyaerts D; Hedou J; Gillard J; Chen H; Tsai ES; Peterson LS; Ando K; Manohar M; Do E; Dhondalay GKR; Fitzpatrick J; Artandi M; Chang I; Snow TT; Chinthrajah RS; Warren CM; Wittman R; Meyerowitz JG; Ganio EA; Stelzer IA; Han X; Verdonk F; Gaudilliere DK; Mukherjee N; Tsai AS; Rumer KK; Jiang S; Valdes Ferrer SI; Kelly JD; Furman D; Aghaeepour N; Angst MS; Boyd SD; Pinsky BA; Nolan GP; Nadeau KC; Gaudilliere B; McIlwain DR
  • bioRxiv 2021[Feb]; ä (ä): ä PMID33594362show ga
  • The biological determinants of the wide spectrum of COVID-19 clinical manifestations are not fully understood. Here, over 1400 plasma proteins and 2600 single-cell immune features comprising cell phenotype, basal signaling activity, and signaling responses to inflammatory ligands were assessed in peripheral blood from patients with mild, moderate, and severe COVID-19, at the time of diagnosis. Using an integrated computational approach to analyze the combined plasma and single-cell proteomic data, we identified and independently validated a multivariate model classifying COVID-19 severity (multi-class AUCtraining = 0.799, p-value = 4.2e-6; multi-class AUCvalidation = 0.773, p-value = 7.7e-6). Features of this high-dimensional model recapitulated recent COVID-19 related observations of immune perturbations, and revealed novel biological signatures of severity, including the mobilization of elements of the renin-angiotensin system and primary hemostasis, as well as dysregulation of JAK/STAT, MAPK/mTOR, and NF-kappaB immune signaling networks. These results provide a set of early determinants of COVID-19 severity that may point to therapeutic targets for the prevention of COVID-19 progression.
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