1. Antiviral potential of human IFN-α subtypes against influenza A H3N2 infection in human lung explants reveals subtype-specific activities
- Author
-
Marlous de Witt, Anmari Christersson, Rainer Wiewrodt, Stefan Hippenstiel, Stephan Ludwig, Nicoletta Matera, Ursula Rescher, Martine Seders, Andreas C. Hocke, Alline da Rocha Matos, Linda Brunotte, Svetlana Rodionycheva, Ulf Dittmer, Kathrin Sutter, Sebastian Schloer, Karsten Wiebe, Peter J Barth, Katharina Wunderlich, Klaus Schughart, Robert Geffers, Katja Honzke, and HZI,Helmholtz-Zentrum für Infektionsforschung GmbH, Inhoffenstr. 7,38124 Braunschweig, Germany.
- Subjects
0301 basic medicine ,Epidemiology ,030106 microbiology ,Immunology ,Medizin ,Alpha interferon ,MxA ,Human lung explant ,Biology ,Virus Replication ,Antiviral Agents ,Microbiology ,Article ,Inhibitory Concentration 50 ,03 medical and health sciences ,Organ Culture Techniques ,In vivo ,Virology ,Influenza, Human ,Drug Discovery ,Humans ,Respiratory system ,Lung ,IFN-α subtype ,Influenza A Virus, H3N2 Subtype ,Interferon-alpha ,Respiratory infection ,Outbreak ,General Medicine ,antiviral ,In vitro ,030104 developmental biology ,Infectious Diseases ,Viral replication ,A549 Cells ,ISG induction ,Cytokines ,Parasitology ,influenza ,Explant culture - Abstract
Influenza is an acute respiratory infection causing high morbidity and mortality in annual outbreaks worldwide. Antiviral drugs are limited and pose the risk of resistance development, calling for new treatment options. IFN-α subtypes are immune-stimulatory cytokines with strong antiviral activities against IAV in vitro and in vivo. However, the clinical use of IFN-α2, the only licensed subtype of this multi-gene family, could not prevent or limit IAV infections in humans. However, the other subtypes were not investigated. Therefore, this study evaluated the induction and antiviral potential of all human IFN-α subtypes during H3N2 IAV infection in human lung explants. We found that subtypes with weak antiviral activities were preferentially induced during IAV infection in human lungs. Intriguingly, non-induced subtypes α16, α5 and α4 suppressed viral replication up to 230-fold more efficiently than α2. Furthermore, our results demonstrate that subtypes with stronger antiviral activities induce higher expression of IAV-specific restriction factors and that MxA expression is a determinant of the subtype-specific antiviral activity towards H3N2 IAV. These results corroborate that IFN-α subtypes exhibit differential antiviral activities and emphasize that subtypes α16, α5 and α4 should be further investigated for the prevention and treatment of severe infections with seasonal H3N2 IAV.
- Published
- 2019
- Full Text
- View/download PDF