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10.1038/srep01686

http://scihub22266oqcxt.onion/10.1038/srep01686
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23594967!3629412!23594967
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suck abstract from ncbi


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pmid23594967      Sci+Rep 2013 ; 3 (ä): 1686
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  • Inhibition of novel beta coronavirus replication by a combination of interferon-alpha2b and ribavirin #MMPMID23594967
  • Falzarano D; de Wit E; Martellaro C; Callison J; Munster VJ; Feldmann H
  • Sci Rep 2013[]; 3 (ä): 1686 PMID23594967show ga
  • The identification of a novel beta coronavirus, nCoV, as the causative agent of severe respiratory illness in humans originating in Saudi Arabia, Qatar and Jordan has raised concerns about the possibility of a coronavirus pandemic similar to that of SARS-CoV. As a definitive treatment regimen has never been thoroughly evaluated for coronavirus infections, there is an urgent need to rapidly identify potential therapeutics to address future cases of nCoV. To determine an intervention strategy, the effect of interferon-alpha2b and ribavirin on nCoV isolate hCoV-EMC/2012 replication in Vero and LLC-MK2 cells was evaluated. hCoV-EMC/2012 was sensitive to both interferon-alpha2b and ribavirin alone in Vero and LLC-MK2 cells, but only at relatively high concentrations; however, when combined, lower concentrations of interferon-alpha2b and ribavirin achieved comparable endpoints. Thus, a combination of interferon-alpha2b and ribavirin, which are already commonly used in the clinic, may be useful for patient management in the event of future nCoV infections.
  • |Animals[MESH]
  • |Chlorocebus aethiops[MESH]
  • |Coronavirus/*drug effects/*physiology[MESH]
  • |Drug Combinations[MESH]
  • |Interferon-alpha/*administration & dosage[MESH]
  • |Ribavirin/*administration & dosage[MESH]
  • |Vero Cells[MESH]


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