Anti-high mobility group box-1 monoclonal antibody treatment of brain edema induced by influenza infection and lipopolysaccharide

J Med Virol. 2018 Jul;90(7):1192-1198. doi: 10.1002/jmv.25076. Epub 2018 Mar 31.

Abstract

Encephalopathy is a major cause of influenza-associated child death and severe neurological sequelae in Japan, highlighting the urgent need for new therapeutic strategies. In this study, we evaluated the effects of anti-high mobility group box-1 monoclonal antibody (α-HMGB1) treatment on brain edema induced by influenza A virus (IAV) and lipopolysaccharide in 4-week-old BALB/c female mice. The results showed that administration of 7.5 mg/kg α-HMGB1 1 h after IAV (A/Puerto Rico/8/34) inoculation significantly alleviated brain edema at 48 h after IAV inoculation, as confirmed by the suppression of Evans Blue dye leakage and matrix metallopeptidase-9 mRNA expression in the brain. Moreover, we also observed suppression of oxidative stress and different cytokines in IAV-inoculated mice. The expression of plasminogen activator inhibitor-1 was also attenuated following treatment with α-HMGB1. Notably, α-HMGB1 treatment had no effect on virus propagation in the lung. In summary, anti-HMGB1 treatment may improve the prognosis in cases with influenza-associated encephalopathy by attenuating brain edema and reducing the inflammatory responses induced by HMGB1.

Keywords: brain edema; encephalopathy; high mobility group box-1; influenza virus; monoclonal antibody.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / administration & dosage*
  • Brain Edema / chemically induced
  • Brain Edema / pathology
  • Brain Edema / therapy*
  • Disease Models, Animal
  • Female
  • HMGB1 Protein / antagonists & inhibitors*
  • HMGB1 Protein / immunology
  • Immunologic Factors / administration & dosage*
  • Japan
  • Lipopolysaccharides / administration & dosage
  • Lipopolysaccharides / toxicity*
  • Mice, Inbred BALB C
  • Orthomyxoviridae Infections / complications*
  • Treatment Outcome

Substances

  • Antibodies, Monoclonal
  • HMGB1 Protein
  • HMGB1 protein, mouse
  • Immunologic Factors
  • Lipopolysaccharides