Radix isatidis Polysaccharides Inhibit Influenza a Virus and Influenza A Virus-Induced Inflammation via Suppression of Host TLR3 Signaling In Vitro

Molecules. 2017 Jan 11;22(1):116. doi: 10.3390/molecules22010116.

Abstract

Influenza remains one of the major epidemic diseases worldwide, and rapid virus replication and collateral lung tissue damage caused by excessive pro-inflammatory host immune cell responses lead to high mortality rates. Thus, novel therapeutic agents that control influenza A virus (IAV) propagation and attenuate excessive pro-inflammatory responses are needed. Polysaccharide extract from Radix isatidis, a traditional Chinese herbal medicine, exerted potent anti-IAV activity against human seasonal influenza viruses (H1N1 and H3N2) and avian influenza viruses (H6N2 and H9N2) in vitro. The polysaccharides also significantly reduced the expression of pro-inflammatory cytokines (IL-6) and chemokines (IP-10, MIG, and CCL-5) stimulated by A/PR/8/34 (H1N1) at a range of doses (7.5 mg/mL, 15 mg/mL, and 30 mg/mL); however, they were only effective against progeny virus at a high dose. Similar activity was detected against inflammation induced by avian influenza virus H9N2. The polysaccharides strongly inhibited the protein expression of TLR-3 induced by PR8, suggesting that they impair the upregulation of pro-inflammatory factors induced by IAV by inhibiting activation of the TLR-3 signaling pathway. The polysaccharide extract from Radix isatidis root therefore has the potential to be used as an adjunct to antiviral therapy for the treatment of IAV infection.

Keywords: Radix isatidis; TLR-3; anti-inflammatory; antiviral; polysaccharides.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / isolation & purification
  • Anti-Inflammatory Agents / pharmacology
  • Antiviral Agents / isolation & purification
  • Antiviral Agents / pharmacology*
  • Bronchi / cytology
  • Bronchi / drug effects
  • Bronchi / immunology
  • Cell Line
  • Cell Survival / drug effects
  • Chemokine CCL5 / genetics
  • Chemokine CCL5 / immunology
  • Chemokine CXCL9 / genetics
  • Chemokine CXCL9 / immunology
  • Chickens
  • Dogs
  • Drugs, Chinese Herbal / chemistry*
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects
  • Epithelial Cells / immunology
  • Gene Expression Regulation
  • Humans
  • Influenza A Virus, H1N1 Subtype / drug effects*
  • Influenza A Virus, H1N1 Subtype / immunology
  • Influenza A Virus, H3N2 Subtype / drug effects*
  • Influenza A Virus, H3N2 Subtype / immunology
  • Influenza A Virus, H9N2 Subtype / drug effects*
  • Influenza A Virus, H9N2 Subtype / immunology
  • Interleukin-10 / genetics
  • Interleukin-10 / immunology
  • Interleukin-6 / genetics
  • Interleukin-6 / immunology
  • Madin Darby Canine Kidney Cells
  • Polysaccharides / isolation & purification
  • Polysaccharides / pharmacology*
  • Signal Transduction / drug effects
  • Signal Transduction / immunology
  • Toll-Like Receptor 3 / antagonists & inhibitors*
  • Toll-Like Receptor 3 / genetics
  • Toll-Like Receptor 3 / immunology
  • Zygote / virology

Substances

  • Anti-Inflammatory Agents
  • Antiviral Agents
  • CCL5 protein, human
  • CXCL9 protein, human
  • Chemokine CCL5
  • Chemokine CXCL9
  • Drugs, Chinese Herbal
  • IL10 protein, human
  • IL6 protein, human
  • Interleukin-6
  • Polysaccharides
  • TLR3 protein, human
  • Toll-Like Receptor 3
  • Interleukin-10
  • banlangen