Direct-acting antivirals and host-targeting strategies to combat enterovirus infections

Curr Opin Virol. 2017 Jun:24:1-8. doi: 10.1016/j.coviro.2017.03.009. Epub 2017 Apr 12.

Abstract

Enteroviruses (e.g., poliovirus, enterovirus-A71, coxsackievirus, enterovirus-D68, rhinovirus) include many human pathogens causative of various mild and more severe diseases, especially in young children. Unfortunately, antiviral drugs to treat enterovirus infections have not been approved yet. Over the past decades, several direct-acting inhibitors have been developed, including capsid binders, which block virus entry, and inhibitors of viral enzymes required for genome replication. Capsid binders and protease inhibitors have been clinically evaluated, but failed due to limited efficacy or toxicity issues. As an alternative approach, host-targeting inhibitors with potential broad-spectrum activity have been identified. Furthermore, drug repurposing screens have recently uncovered promising new inhibitors with disparate viral and host targets. Together, these findings raise hope for the development of (broad-range) anti-enteroviral drugs.

Publication types

  • Review

MeSH terms

  • Animals
  • Antiviral Agents / administration & dosage
  • Antiviral Agents / therapeutic use*
  • Capsid / drug effects
  • Cyclophilins / therapeutic use
  • Drug Repositioning
  • Enterovirus / drug effects*
  • Enterovirus Infections / drug therapy*
  • Humans
  • Mice
  • Poliovirus / drug effects
  • Protease Inhibitors / therapeutic use
  • Rhinovirus / drug effects
  • Virus Internalization / drug effects
  • Virus Replication / drug effects

Substances

  • Antiviral Agents
  • Protease Inhibitors
  • Cyclophilins