Modeling of viral-bacterial coinfections at the molecular level using agonists of innate immunity receptors

Dokl Biochem Biophys. 2016 Nov;471(1):393-395. doi: 10.1134/S1607672916060053. Epub 2017 Jan 6.

Abstract

The combined effect of innate immunity receptors in viral-bacterial coinfections was studied in vitro using the primary culture of murine macrophages activated by different combinations of ligands of innate immunity receptors belonging to the family of Toll-like receptors. The activation of macrophages first with a viral ligand and then with a bacterial one significantly decreased the expression of proinflammatory cytokine genes. Such attenuation of immune responses may occur during the development of bacterial complications in viral infections.

MeSH terms

  • Aminoquinolines / pharmacology
  • Animals
  • Bacterial Infections / immunology
  • Bacterial Infections / metabolism
  • Bone Marrow
  • Cells, Cultured
  • Coinfection / immunology
  • Coinfection / metabolism
  • Cytokines / genetics*
  • Disease Models, Animal
  • Imiquimod
  • Immunity, Innate
  • Interleukin-1beta / genetics
  • Interleukin-1beta / metabolism
  • Interleukin-6 / genetics
  • Interleukin-6 / metabolism
  • Ligands
  • Lipopolysaccharides / immunology
  • Macrophage Activation*
  • Macrophages / immunology*
  • Membrane Glycoproteins / agonists
  • Membrane Glycoproteins / immunology*
  • Membrane Glycoproteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • RNA, Messenger / metabolism
  • Toll-Like Receptor 4 / agonists
  • Toll-Like Receptor 4 / immunology*
  • Toll-Like Receptor 4 / metabolism
  • Toll-Like Receptor 7 / agonists
  • Toll-Like Receptor 7 / immunology*
  • Toll-Like Receptor 7 / metabolism
  • Toll-Like Receptors / agonists*
  • Toll-Like Receptors / metabolism*
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism
  • Virus Diseases / immunology
  • Virus Diseases / metabolism

Substances

  • Aminoquinolines
  • Cytokines
  • IL1B protein, mouse
  • Interleukin-1beta
  • Interleukin-6
  • Ligands
  • Lipopolysaccharides
  • Membrane Glycoproteins
  • RNA, Messenger
  • Tlr4 protein, mouse
  • Tlr7 protein, mouse
  • Toll-Like Receptor 4
  • Toll-Like Receptor 7
  • Toll-Like Receptors
  • Tumor Necrosis Factor-alpha
  • Imiquimod