Kinase control prevents HIV-1 reactivation in spite of high levels of induced NF-κB activity

J Virol. 2012 Apr;86(8):4548-58. doi: 10.1128/JVI.06726-11. Epub 2012 Feb 15.

Abstract

Despite its clinical importance, the molecular biology of HIV-1 latency control is at best partially understood, and the literature remains conflicting. The most recent description that latent HIV-1 is integrated into actively expressed host genes has further confounded the situation. This lack of molecular understanding complicates our efforts to identify therapeutic compounds or strategies that could reactivate latent HIV-1 infection in patients, a prerequisite for the eradication of HIV-1 infection. Currently, many therapeutic development efforts operate under the assumption that a restrictive histone code could govern latent infection and that either dissipation of the histone-based restrictions or NF-κB activation could be sufficient to trigger HIV-1 reactivation. We here present data that suggest an additional, higher level of molecular control. During a high-content drug screening effort, we identified AS601245 as a potent inhibitor of HIV-1 reactivation in latently infected primary T cells and T cell lines. In either system, AS601245 inhibited HIV-1 reactivation despite high levels of induced NF-κB activation. This finding suggests the presence of a gatekeeper kinase activity that controls latent HIV-1 infection even in the presence of high levels of NF-κB activity. Potential therapeutic stimuli that do not target this gatekeeper kinase will likely fail to trigger efficient system-wide HIV-1 reactivation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acetonitriles / pharmacology
  • Benzothiazoles / pharmacology
  • Cell Line
  • Gene Expression Regulation / drug effects
  • HIV-1 / drug effects
  • HIV-1 / metabolism*
  • Humans
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • NF-kappa B / metabolism*
  • Phosphotransferases / antagonists & inhibitors
  • Phosphotransferases / metabolism*
  • Positive Transcriptional Elongation Factor B / metabolism
  • Protein Binding / drug effects
  • Protein Kinase Inhibitors / pharmacology
  • RNA-Binding Proteins / metabolism
  • Signal Transduction / drug effects
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / virology
  • Transcription Factors
  • Virus Activation* / drug effects
  • Virus Latency / drug effects

Substances

  • 1,3-benzothiazol-2-yl(2-((2-(3-pyridinyl)ethyl)amino)-4-pyrimidinyl)acetonitrile
  • Acetonitriles
  • Benzothiazoles
  • HEXIM1 protein, human
  • NF-kappa B
  • Protein Kinase Inhibitors
  • RNA-Binding Proteins
  • Transcription Factors
  • Phosphotransferases
  • Positive Transcriptional Elongation Factor B
  • JNK Mitogen-Activated Protein Kinases