Polymeric inhibitor of influenza virus attachment protects mice from experimental influenza infection

Antiviral Res. 2002 Jul;55(1):201-5. doi: 10.1016/s0166-3542(02)00020-7.

Abstract

Synthetic sialic acid-containing macromolecules inhibit influenza virus attachment to target cells and suppress the virus-mediated hemagglutination and neutralize virus infectivity in cell culture. To test the protective effects of attachment inhibitors in vivo, mice were infected with mouse-adapted influenza virus A/Aichi/2/68 (H3N2) and treated with synthetic polyacrylamide-based sialylglycopolymer PAA-YDS bearing moieties of (Neu5Acalpha2-6Galbeta1-4GlcNAcbeta1-2Manalpha1)2-3,6Manbeta1-4GlcNAcbeta1-4GlcNAc. Single intranasal inoculations with PAA-YDS 30 min before or 10 min after infection increased the survival of mice (P<0.01). Multiple treatments with aerosolized PAA-YDS on days 2-5 post infection also increased survival (P<0.01), alleviated disease symptoms, and decreased lesions in the mouse lungs. These data suggest that synthetic polyvalent inhibitors of virus attachment can be used for prevention and treatment of influenza.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrylic Resins / chemistry
  • Acrylic Resins / therapeutic use
  • Administration, Inhalation
  • Animals
  • Antiviral Agents / therapeutic use*
  • Carbohydrate Sequence
  • Disease Models, Animal
  • Drug Design
  • Lung / drug effects
  • Lung / pathology
  • Mice
  • Molecular Sequence Data
  • Oligosaccharides / chemistry
  • Oligosaccharides / therapeutic use*
  • Orthomyxoviridae / drug effects*
  • Orthomyxoviridae / physiology
  • Orthomyxoviridae Infections / drug therapy*
  • Orthomyxoviridae Infections / pathology
  • Virus Replication

Substances

  • Acrylic Resins
  • Antiviral Agents
  • Oligosaccharides
  • sialooligosaccharides
  • polyacrylamide