Anti-high mobility group box-1 monoclonal antibody treatment of brain edema induced by influenza infection and lipopolysaccharide.
Nobuyuki NosakaKazuki HatayamaMutsuko YamadaYousuke FujiiMasato YashiroHidenori WakeHirokazu TsukaharaMasahiro NishiboriTsuneo MorishimaPublished in: Journal of medical virology (2018)
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.
Keyphrases
- monoclonal antibody
- white matter
- resting state
- early onset
- metabolic syndrome
- multiple sclerosis
- immune response
- inflammatory response
- type diabetes
- mental health
- toll like receptor
- dna damage
- poor prognosis
- cerebral ischemia
- signaling pathway
- ischemia reperfusion injury
- clinical trial
- long non coding rna
- binding protein
- heat stress
- double blind