The toll-like receptor agonist imiquimod is active against prions

PLoS One. 2013 Aug 16;8(8):e72112. doi: 10.1371/journal.pone.0072112. eCollection 2013.

Abstract

Using a yeast-based assay, a previously unsuspected antiprion activity was found for imiquimod (IQ), a potent Toll-like receptor 7 (TLR7) agonist already used for clinical applications. The antiprion activity of IQ was first detected against yeast prions [PSI (+) ] and [URE3], and then against mammalian prion both ex vivo in a cell-based assay and in vivo in a transgenic mouse model for prion diseases. In order to facilitate structure-activity relationship studies, we conducted a new synthetic pathway which provides a more efficient means of producing new IQ chemical derivatives, the activity of which was tested against both yeast and mammalian prions. The comparable antiprion activity of IQ and its chemical derivatives in the above life forms further emphasizes the conservation of prion controlling mechanisms throughout evolution. Interestingly, this study also demonstrated that the antiprion activity of IQ and IQ-derived compounds is independent from their ability to stimulate TLRs. Furthermore, we found that IQ and its active chemical derivatives inhibit the protein folding activity of the ribosome (PFAR) in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminoquinolines / chemical synthesis
  • Aminoquinolines / pharmacology*
  • Animals
  • Cell Line
  • Drug Evaluation, Preclinical
  • Glutathione Peroxidase / metabolism*
  • Guanosine / analogs & derivatives
  • Guanosine / pharmacology
  • Humans
  • Imidazoles / pharmacology
  • Imiquimod
  • Membrane Glycoproteins / agonists
  • Membrane Glycoproteins / metabolism
  • Mice
  • Peptide Termination Factors / metabolism*
  • PrPSc Proteins / metabolism
  • Prion Diseases / drug therapy*
  • Prion Diseases / metabolism
  • Prions / metabolism*
  • Protein Folding
  • Saccharomyces cerevisiae / drug effects
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae Proteins / metabolism*
  • Structure-Activity Relationship
  • Toll-Like Receptor 7 / agonists
  • Toll-Like Receptor 7 / metabolism
  • Toll-Like Receptor 8 / agonists
  • Toll-Like Receptor 8 / metabolism

Substances

  • Aminoquinolines
  • Imidazoles
  • Membrane Glycoproteins
  • Peptide Termination Factors
  • PrPSc Proteins
  • Prions
  • SUP35 protein, S cerevisiae
  • Saccharomyces cerevisiae Proteins
  • TLR8 protein, mouse
  • Tlr7 protein, mouse
  • Toll-Like Receptor 7
  • Toll-Like Receptor 8
  • gardiquimod
  • Guanosine
  • loxoribine
  • Glutathione Peroxidase
  • URE2 protein, S cerevisiae
  • Imiquimod
  • resiquimod

Grants and funding

This work was supported by an Agence Nationale de la Recherche "blanche" from the French government, a Contrat Jeune Chercheur from Institut National de la Santé et de la Recherche Médicale and the SSF-Dalen (Sweden-France Bilateral Collaboration) Program (to MB & SS). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.