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Are we fully exploiting type I Interferons in today's fight against COVID-19 pandemic?
[Display omitted] •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 promis...
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Published in: | Cytokine & growth factor reviews 2020-08, Vol.54, p.43-50 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•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.
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. |
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ISSN: | 1359-6101 1879-0305 |
DOI: | 10.1016/j.cytogfr.2020.07.010 |