Integrated pipeline for the accelerated discovery of antiviral antibody therapeutics. Academic Article uri icon

Overview

abstract

  • The emergence and re-emergence of highly virulent viral pathogens with the potential to cause a pandemic creates an urgent need for the accelerated discovery of antiviral therapeutics. Antiviral human monoclonal antibodies (mAbs) are promising candidates for the prevention and treatment of severe viral diseases, but their long development timeframes limit their rapid deployment and use. Here, we report the development of an integrated sequence of technologies, including single-cell mRNA-sequence analysis, bioinformatics, synthetic biology and high-throughput functional analysis, that enables the rapid discovery of highly potent antiviral human mAbs, the activity of which we validated in vivo. In a 78-d study modelling the deployment of a rapid response to an outbreak, we isolated more than 100 human mAbs that are specific to Zika virus, assessed their function, identified that 29 of these mAbs have broadly neutralizing activity, and verified the therapeutic potency of the lead candidates in mice and non-human primate models of infection through the delivery of an antibody-encoding mRNA formulation and of the respective IgG antibody. The pipeline provides a roadmap for rapid antibody-discovery programmes against viral pathogens of global concern.

authors

publication date

  • August 3, 2020

Research

keywords

  • Antibodies, Monoclonal
  • Antibodies, Viral
  • Antiviral Agents
  • Drug Discovery
  • Zika Virus

Identity

PubMed Central ID

  • PMC7655621

Scopus Document Identifier

  • 85088873601

Digital Object Identifier (DOI)

  • 10.1038/s41551-020-0594-x

PubMed ID

  • 32747832

Additional Document Info

volume

  • 4

issue

  • 11