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10.1016/j.antiviral.2020.104811

http://scihub22266oqcxt.onion/10.1016/j.antiviral.2020.104811
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suck abstract from ncbi


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pmid32360182      Antiviral+Res 2020 ; 179 (ä): 104811
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  • Antiviral activities of type I interferons to SARS-CoV-2 infection #MMPMID32360182
  • Mantlo E; Bukreyeva N; Maruyama J; Paessler S; Huang C
  • Antiviral Res 2020[Jul]; 179 (ä): 104811 PMID32360182show ga
  • There is an urgent need to identify antivirals to curtail the COVID-19 pandemic. Herein, we report the sensitivity of SARS-CoV-2 to recombinant human interferons alpha and beta (IFNalpha/beta). Treatment with IFN-alpha or IFN-beta at a concentration of 50 international units (IU) per milliliter reduces viral titers by 3.4 log or over 4 log, respectively, in Vero cells. The EC(50) of IFN-alpha and IFN-beta treatment is 1.35 IU/ml and 0.76 IU/ml, respectively, in Vero cells. These results suggest that SARS-CoV-2 is more sensitive than many other human pathogenic viruses, including SARS-CoV. Overall, our results demonstrate the potential efficacy of human Type I IFN in suppressing SARS-CoV-2 infection, a finding which could inform future treatment options for COVID-19.
  • |Animals[MESH]
  • |Antiviral Agents/*pharmacology[MESH]
  • |Betacoronavirus/*drug effects[MESH]
  • |COVID-19[MESH]
  • |Chlorocebus aethiops[MESH]
  • |Coronavirus Infections/*drug therapy/immunology/virology[MESH]
  • |Humans[MESH]
  • |Immunity, Innate[MESH]
  • |Interferon Type I/*pharmacology[MESH]
  • |Interferon-alpha/pharmacology[MESH]
  • |Interferon-beta/pharmacology[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*drug therapy/immunology/virology[MESH]
  • |Recombinant Proteins/pharmacology[MESH]
  • |SARS-CoV-2[MESH]
  • |Severe Acute Respiratory Syndrome/*drug therapy/immunology/virology[MESH]
  • |Vero Cells[MESH]
  • |Viral Load/drug effects[MESH]


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