Abstract

The latest coronavirus disease outbreak, COVID-19, has brought attention to viral infections which have posed serious health threats to humankind throughout history. The rapid global spread of COVID-19 is attributed to the increased human mobility of today’s world, yet the threat of viral infections to global public health is expected to increase continuously in part due to increasing human–animal interface. Development of antiviral agents is crucial to combat both existing and novel viral infections. Recently, there is a growing interest in peptide/protein-based drug molecules. Antibodies are becoming especially predominant in the drug market. Indeed, in a remarkably short period, four antibody therapeutics were authorized for emergency use in COVID-19 treatment in the US, Russia, and India as of November 2020. Phage display has been one of the most widely used screening methods for peptide/antibody drug discovery. Several phage display-derived biologics are already in the market, and the expiration of intellectual property rights of phage-display antibody discovery platforms suggests an increment in antibody drugs in the near future. This review summarizes the most common phage display libraries used in antiviral discovery, highlights the approaches employed to enhance the antiviral potency of selected peptides/antibody fragments, and finally provides a discussion about the present status of the developed antivirals in clinic.

Highlights

  • Since ancient times, infectious diseases have been one of the leading causes of death and disability worldwide

  • The latest outbreak of coronavirus emerged at the end of 2019 in Wuhan, China from a causative agent closely related to Severe acute respiratory syndrome (SARS)-CoV, namely SARS-CoV-2, while the disease it causes was named COVID-19 [17]

  • A synthetic human ScFv phage display library was screened against Ebola filovirus (EBOV)’s viral protein 35 (VP35), which is a cofactor of the viral RNA polymerase complex as well as a double-stranded RNA-binding protein interfering with the host immune response by blocking the interferon (IFN)-mediated antiviral activity [127]

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Summary

Introduction

Infectious diseases have been one of the leading causes of death and disability worldwide. Type I interferon (IFN), a therapeutic agent to treat viral infections, was used as a target to screen 7-mer phage display libraries to discover antiviral peptides [67]. A murine brain cDNA phage display library was screened against the West Nile virus (WNV) envelope (E) protein to select a peptide with inhibitory activity on virus–host cell interaction [70]. A synthetic human ScFv phage display library was screened against Ebola filovirus (EBOV)’s viral protein 35 (VP35), which is a cofactor of the viral RNA polymerase complex as well as a double-stranded RNA-binding protein interfering with the host immune response by blocking the interferon (IFN)-mediated antiviral activity [127]. Plaque reduction neutralization assay demonstrated that T166 and F21 ScFvs could inhibit plaque formation of three different rabies virus strains (CVS-II, CQ92, and SBD) in Vero cells

Nanobodies
Other Protein Scaffolds
Modification of the Peptide Backbone to Enhance Stability
Conversion of Antibody Fragments into Whole IgG Antibodies
Findings
Perspective
Full Text
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