Experimental and natural evidence of SARS-CoV-2 infection-induced activation of type I interferon responses

Author:

Banerjee ArinjayORCID,El-Sayes Nader,Budylowski Patrick,Richard Daniel,Maan Hassaan,Aguiar Jennifer A.,Baid Kaushal,D’Agostino Michael R.,Ang Jann Catherine,Tremblay Benjamin J.-M.,Afkhami Sam,Karimzadeh MehranORCID,Irving Aaron T.,Yip Lily,Ostrowski Mario,Hirota Jeremy A.,Kozak Robert,Capellini Terence D.,Miller Matthew S.,Wang Bo,Mubareka Samira,McGeer Allison J.,McArthur Andrew G.,Doxey Andrew C.,Mossman Karen

Abstract

SUMMARYType I interferons (IFNs) are our first line of defence against a virus. Protein over-expression studies have suggested the ability of SARS-CoV-2 proteins to block IFN responses. Emerging data also suggest that timing and extent of IFN production is associated with manifestation of COVID-19 severity. In spite of progress in understanding how SARS-CoV-2 activates antiviral responses, mechanistic studies into wildtype SARS-CoV-2-mediated induction and inhibition of human type I IFN responses are lacking. Here we demonstrate that SARS-CoV-2 infection induces a mild type I IFN response in vitro and in moderate cases of COVID-19. In vitro stimulation of type I IFN expression and signaling in human airway epithelial cells is associated with activation of canonical transcriptions factors, and SARS-CoV-2 is unable to inhibit exogenous induction of these responses. Our data demonstrate that SARS-CoV-2 is not adept in blocking type I IFN responses and provide support for ongoing IFN clinical trials.

Publisher

Cold Spring Harbor Laboratory

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