4.7 Article

A painful lesson from the COVID-19 pandemic: the need for broad-spectrum, host-directed antivirals

Journal

JOURNAL OF TRANSLATIONAL MEDICINE
Volume 18, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12967-020-02476-9

Keywords

COVID-19; Broad-spectrum antivirals; Mechanism of action (MOA); Pandemics; Drug discovery and development; SARS-CoV-2; Host-directed antivirals; Antiviral drug design; Coronavirus (CoV); Drug design strategies; Prophylactic antiviral therapy

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While the COVID-19 pandemic has spurred intense research and collaborative discovery worldwide, the development of a safe, effective, and targeted antiviral from the ground up is time intensive. Therefore, most antiviral discovery efforts are focused on the re-purposing of clinical stage or approved drugs. While emerging data on drugs undergoing COVID-19 repurpose are intriguing, there is an undeniable need to develop broad-spectrum antivirals to prevent future viral pandemics of unknown origin. The ideal drug to curtail rapid viral spread would be a broad-acting agent with activity against a wide range of viruses. Such a drug would work by modulating host-proteins that are often shared by multiple virus families thereby enabling preemptive drug development and therefore rapid deployment at the onset of an outbreak. Targeting host-pathways and cellular proteins that are hijacked by viruses can potentially offer broad-spectrum targets for the development of future antiviral drugs. Such host-directed antivirals are also likely to offer a higher barrier to the development and selection of drug resistant mutations. Given that most approved antivirals do not target host-proteins, we reinforce the need for the development of such antivirals that can be used in pre- and post-exposure populations.

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