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Are we fully exploiting type I Interferons in today's fight against COVID-19 pandemic?

Authors :
Eleonora Aricò
Luciano Castiello
Laura Bracci
Sandra Gessani
Filippo Belardelli
Source :
Cytokine & Growth Factor Reviews, Cytokine & growth factor reviews 54 (2020): 43–50. doi:10.1016/j.cytogfr.2020.07.010, info:cnr-pdr/source/autori:Arico E.; Bracci L.; Castiello L.; Gessani S.; Belardelli F./titolo:Are we fully exploiting type I Interferons in today's fight against COVID-19 pandemic?/doi:10.1016%2Fj.cytogfr.2020.07.010/rivista:Cytokine & growth factor reviews/anno:2020/pagina_da:43/pagina_a:50/intervallo_pagine:43–50/volume:54
Publication Year :
2020

Abstract

Graphical abstract<br />Highlights • IFN-I, in particular IFN-β, are promising drugs for SARS-CoV2 infection • Early infection in elderly patients is the best setting to exploit IFN-I immunomodulatory activity • Caution should be given in using continuous IFN-I treatments at high doses. • Mucosal IFN-I delivery is promising but deserves further clinical investigation • Attention should be paid to IFN-I treatment in patients with severe COVID-19<br />Coronavirus disease 2019 (COVID-19) first emerged in late 2019 in China. At the time of writing, its causative agent SARS-CoV-2 has spread worldwide infecting over 9 million individuals and causing more than 460,000 deaths. In the absence of vaccines, we are facing the dramatic challenge of controlling COVID-19 pandemic. Among currently available drugs, type I Interferons (IFN-I) – mainly IFN-α and β –represent ideal candidates given their direct and immune-mediated antiviral effects and the long record of clinical use. However, the best modalities of using these cytokines in SARS-CoV-2 infected patients is a matter of debate. Here, we discuss how we can exploit the current knowledge on IFN-I system to tailor the most promising dosing, timing and route of administration of IFN-I to the disease stage, with the final aim of making these cytokines a valuable therapeutic strategy in today's fight against COVID-19 pandemic.

Details

ISSN :
18790305
Volume :
54
Database :
OpenAIRE
Journal :
Cytokinegrowth factor reviews
Accession number :
edsair.doi.dedup.....33910a513bf151676e22e8db5acbfecf