Compound A, a dissociated glucocorticoid receptor modulator, reduces dengue virus-induced cytokine secretion and dengue virus production

Biochem Biophys Res Commun. 2013 Jun 28;436(2):283-8. doi: 10.1016/j.bbrc.2013.05.094. Epub 2013 Jun 4.

Abstract

Dengue Virus (DENV) infection is an important mosquito-borne viral disease and its clinical symptoms range from a predominantly febrile disease, dengue fever (DF), to dengue hemorrhagic fever (DHF) and dengue shock syndrome (DSS). Increased levels of cytokines - the so-called 'cytokine storm', contribute to the pathogenesis of DHF/DSS. In this study, we compared the expression of cytokine genes between mock-infected and DENV-infected HepG2 cells using a real-time PCR array and revealed several up-regulated chemokines and cytokines, including CXCL10 and TNF-α. Compound A (CpdA), a plant-derived phenyl aziridine precursor containing anti-inflammatory action and acting as a dissociated nonsteroidal glucocorticoid receptor modulator, was selected as a candidate agent to modulate secretion of DENV-induced cytokines. CpdA is not a glucocorticoid but has an anti-inflammatory effect with no metabolic side effects as steroidal ligands. CpdA significantly reduced DENV-induced CXCL10 and TNF-α secretion and decreased leukocyte migration indicating for the first time the therapeutic potential of CpdA in decreasing massive immune activation during DENV infection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetates / pharmacology*
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Cell Line
  • Cell Migration Assays, Leukocyte
  • Chemokine CXCL10 / genetics
  • Chemokine CXCL10 / metabolism
  • Chemotaxis / drug effects
  • Chlorocebus aethiops
  • Cytokines / genetics
  • Cytokines / metabolism*
  • Dengue Virus / growth & development*
  • Dengue Virus / physiology
  • Flow Cytometry
  • Gene Expression / drug effects
  • Hep G2 Cells
  • Host-Pathogen Interactions
  • Humans
  • Liver Neoplasms / genetics
  • Liver Neoplasms / metabolism
  • Liver Neoplasms / virology
  • Plant Extracts / pharmacology*
  • Receptors, Glucocorticoid / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Salsola / chemistry
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism
  • Tyramine / analogs & derivatives*
  • Tyramine / pharmacology

Substances

  • 2-(4-acetoxyphenyl)-2-chloro-N-methylethylamine
  • Acetates
  • Anti-Inflammatory Agents, Non-Steroidal
  • Chemokine CXCL10
  • Cytokines
  • Plant Extracts
  • Receptors, Glucocorticoid
  • Tumor Necrosis Factor-alpha
  • Tyramine