RIG-I Activation Protects and Rescues from Lethal Influenza Virus Infection and Bacterial Superinfection

Mol Ther. 2017 Sep 6;25(9):2093-2103. doi: 10.1016/j.ymthe.2017.07.003. Epub 2017 Jul 8.

Abstract

Influenza A virus infection causes substantial morbidity and mortality in seasonal epidemic outbreaks, and more efficient treatments are urgently needed. Innate immune sensing of viral nucleic acids stimulates antiviral immunity, including cell-autonomous antiviral defense mechanisms that restrict viral replication. RNA oligonucleotide ligands that potently activate the cytoplasmic helicase retinoic-acid-inducible gene I (RIG-I) are promising candidates for the development of new antiviral therapies. Here, we demonstrate in an Mx1-expressing mouse model of influenza A virus infection that a single intravenous injection of low-dose RIG-I ligand 5'-triphosphate RNA (3pRNA) completely protected mice from a lethal challenge with influenza A virus for at least 7 days. Furthermore, systemic administration of 3pRNA rescued mice with pre-established fulminant influenza infection and prevented the fatal effects of a streptococcal superinfection. Type I interferon, but not interferon-λ, was required for the therapeutic effect. Our results suggest that the use of RIG-I activating oligonucleotide ligands has the clinical potential to confine influenza epidemics when a strain-specific vaccine is not yet available and to reduce lethality of influenza in severely infected patients.

Keywords: 5’ triphosphate RNA; RIG-I; antivirals; immunostimulatory oligonucleotides; immunotherapy; influenza virus; innate immunity; negative strand RNA virus; type I interferon; type III interferon.

MeSH terms

  • Animals
  • Bacterial Infections*
  • Chemokine CXCL10 / metabolism
  • Influenza A virus* / immunology
  • Interferon Type I / metabolism
  • Ligands
  • Lung / immunology
  • Lung / metabolism
  • Lung / pathology
  • Lung / virology
  • Membrane Proteins / agonists
  • Membrane Proteins / metabolism*
  • Mice
  • Mice, Transgenic
  • Nerve Tissue Proteins / agonists
  • Nerve Tissue Proteins / metabolism*
  • Oligonucleotides / administration & dosage
  • Oligonucleotides / genetics
  • Orthomyxoviridae Infections / metabolism*
  • Orthomyxoviridae Infections / mortality
  • Orthomyxoviridae Infections / virology*
  • Protective Agents / administration & dosage
  • RNA / administration & dosage
  • RNA / genetics
  • Receptors, Cell Surface
  • Superinfection*
  • Survival Analysis
  • Toll-Like Receptors / metabolism

Substances

  • Chemokine CXCL10
  • Interferon Type I
  • Ligands
  • Membrane Proteins
  • Nerve Tissue Proteins
  • Oligonucleotides
  • Protective Agents
  • Receptors, Cell Surface
  • Robo3 protein, mouse
  • Toll-Like Receptors
  • RNA