Novel capsid binder and PI4KIIIbeta inhibitors for EV-A71 replication inhibition

Yong Wah Tan1, Wan Keat Yam1, Rachel Jia Wen Kooi1

  • 1Collaborative and Translation Unit for HFMD, Institute of Molecular and Cell Biology, Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.

Scientific Reports
|May 7, 2021
PubMed

Insights

Two new antiviral compounds, G197 and N373, show promise in treating Enterovirus A71 (EV-A71) infections. Combined treatment significantly improved survival rates and reduced pathology in mice infected with EV-A71.

Area of Science:

  • Virology
  • Infectious Diseases
  • Pharmacology

Background:

  • Hand, Foot and Mouth Disease (HFMD) is a contagious viral illness.
  • Enterovirus A71 (EV-A71) causes severe neurological complications and fatalities.
  • No effective antivirals or widely available vaccines exist for EV-A71.

Purpose of the Study:

  • Evaluate two novel antiviral compounds against EV-A71.
  • Assess the efficacy of a viral capsid inhibitor (G197) and a host-targeting inhibitor (N373).
  • Investigate the combined therapeutic potential of G197 and N373.

Main Methods:

  • In vitro and in vivo studies were conducted.
  • Compounds G197 and N373 were tested against EV-A71.
  • Efficacy was evaluated in infected mouse models.

Main Results:

  • Both G197 and N373 demonstrated antiviral activity against EV-A71.
  • Combination therapy significantly improved survival rates in infected mice.
  • Combined treatment reduced disease pathology in the animal model.

Conclusions:

  • G197 and N373 represent potential therapeutic agents for EV-A71 infections.
  • Combination therapy offers a promising strategy to combat EV-A71.
  • Further research is warranted to develop treatments for EV-A71.