Inhibition of viral replication reverses respiratory syncytial virus-induced NF-kappaB activation and interleukin-8 gene expression in A549 cells

J Virol. 1996 Dec;70(12):9079-82. doi: 10.1128/JVI.70.12.9079-9082.1996.

Abstract

Previous studies have demonstrated that respiratory syncytial virus (RSV) infection of airway epithelial cells results in the expression of a number of cytokines, such as interleukin-8 (IL-8), that are transcriptionally regulated by nuclear factor kappaB (NF-kappaB). In the studies reported here, we demonstrate that treatment of RSV-infected A549 cells with 100 microg of ribavirin (a viral replication inhibitor) per ml results in reversal of RSV-induced NF-kappaB activation, IL-8 mRNA expression, and IL-8 protein production in A549 cells. These data confirm that viral replication is a key step in RSV-induced NF-kappaB activation and IL-8 production.

MeSH terms

  • Antiviral Agents / pharmacology*
  • Binding Sites
  • Gene Expression
  • Humans
  • Interleukin-8 / genetics
  • Interleukin-8 / metabolism*
  • NF-kappa B / drug effects
  • NF-kappa B / metabolism*
  • RNA, Messenger
  • Respiratory Syncytial Viruses / drug effects*
  • Respiratory Syncytial Viruses / metabolism
  • Respiratory Syncytial Viruses / physiology
  • Ribavirin / pharmacology*
  • Transcriptional Activation / drug effects*
  • Tumor Cells, Cultured
  • Virus Replication / drug effects

Substances

  • Antiviral Agents
  • Interleukin-8
  • NF-kappa B
  • RNA, Messenger
  • Ribavirin