Journal
ANTIVIRAL RESEARCH
Volume 179, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.antiviral.2020.104811
Keywords
SARS-CoV-2; COVID-19; Interferon; Antiviral therapy; Innate immune
Categories
Funding
- NIH [AI060549]
- Public Health Service [RO1AI093445, RO1AI129198]
- John. S. Dunn Distinguished Chair in Biodefense endowment
- UTMB Commitment Fund [P84373]
- Department of Pathology Pilot Grant
- Public Health Service award [5UC7AI094660]
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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 (IFN alpha/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 EC50 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-CoV2 infection, a finding which could inform future treatment options for COVID-19.
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