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10.1016/j.isci.2021.103672

http://scihub22266oqcxt.onion/10.1016/j.isci.2021.103672
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suck abstract from ncbi


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pmid34957382      iScience 2022 ; 25 (1): 103672
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  • Integrated miRNA/cytokine/chemokine profiling reveals severity-associated step changes and principal correlates of fatality in COVID-19 #MMPMID34957382
  • Wilson JC; Kealy D; James SR; Plowman T; Newling K; Jagger C; Filbey K; Mann ER; Konkel JE; Menon M; Knight SB; Simpson A; Prihartadi A; Forshaw G; Todd N; Yates DRA; Grainger JR; Hussell T; Kaye PM; Signoret N; Lagos D
  • iScience 2022[Jan]; 25 (1): 103672 PMID34957382show ga
  • Inflammatory cytokines and chemokines (CC) drive COVID-19 pathology. Yet, patients with similar circulating CC levels present with different disease severity. Here, we determined 171 microRNAomes from 58 hospitalized COVID-19 patients (Cohort 1) and levels of 25 cytokines and chemokines (CC) in the same samples. Combining microRNA (miRNA) and CC measurements allowed for discrimination of severe cases with greater accuracy than using miRNA or CC levels alone. Severity group-specific associations between miRNAs and COVID-19-associated CC (e.g., IL6, CCL20) or clinical hallmarks of COVID-19 (e.g., neutrophilia, hypoalbuminemia) separated patients with similar CC levels but different disease severity. Analysis of an independent cohort of 108 patients from a different center (Cohort 2) demonstrated feasibility of CC/miRNA profiling in leftover hospital blood samples with similar severe disease CC and miRNA profiles, and revealed CCL20, IL6, IL10, and miR-451a as key correlates of fatal COVID-19. These findings highlight that systemic miRNA/CC networks underpin severe COVID-19.
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