Natural Products as a Paradigm for the Treatment of Coxsackievirus - induced Myocarditis

Curr Top Med Chem. 2020;20(8):607-616. doi: 10.2174/1568026620666200129094516.

Abstract

Coxsackievirus B3 (CVB3), a member of the Picornaviridae family, is considered to be one of the most important infectious agents to cause virus-induced myocarditis. Despite improvements in studying viral pathology, structure and molecular biology, as well as diagnosis of this disease, there is still no virus-specific drug in clinical use. Structural and nonstructural proteins produced during the coxsackievirus life cycle have been identified as potential targets for blocking viral replication at the step of attachment, entry, uncoating, RNA and protein synthesis by synthetic or natural compounds. Moreover, WIN (for Winthrop) compounds and application of nucleic-acid based strategies were shown to target viral capsid, entry and viral proteases, but have not reached to the clinical trials as a successful antiviral agent. There is an urgent need for diverse molecular libraries for phenotype-selective and high-throughput screening.

Keywords: Antiviral agent; Coxsackievirus; Myocarditis; Natural Products; Picornaviridae; Viral pathology..

Publication types

  • Review

MeSH terms

  • Animals
  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology*
  • Biological Products / chemistry
  • Biological Products / pharmacology*
  • Coxsackievirus Infections / drug therapy*
  • Coxsackievirus Infections / virology
  • Enterovirus / drug effects*
  • Humans
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Myocarditis / drug therapy*
  • Myocarditis / virology

Substances

  • Antiviral Agents
  • Biological Products