Interleukin-21 inhibits HBV replication in vitro

Antivir Ther. 2015;20(6):583-90. doi: 10.3851/IMP2950. Epub 2015 Mar 16.

Abstract

Background: Cytokines are crucial factors in the non-cytolytic antiviral process to inhibit HBV gene expression and replication. Interleukin (IL)-21 has been suggested to play an important role in HBV infection, but it remains unknown whether IL-21 can inhibit HBV replication or how it inhibits HBV replication.

Methods: In this study, we investigated the influence of IL-21 on HBV replication based on human hepatoma Huh7.93 cells co-cultured with human peripheral blood mononuclear cells (PBMCs) and the possible correlation among IL-21, interferon-γ, tumour necrosis factor-α and IL-10.

Results: We demonstrated that the decrease of IL-21 expression and the increase of IL-10 expression in PBMCs could promote HBV replication in vitro. We further revealed that IL-21 is not only able to effectively suppress HBV replication directly but also reduce HBV replication by inhibition of IL-10 secretion.

Conclusions: Our results provide important evidence for the non-cytolytic antiviral mechanism mediated by cytokines and their interactions in chronic hepatitis B.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line, Tumor
  • Coculture Techniques
  • DNA, Viral / antagonists & inhibitors*
  • DNA, Viral / genetics
  • Hepatitis B virus / drug effects*
  • Hepatitis B virus / genetics
  • Hepatitis B virus / growth & development
  • Hepatitis B, Chronic / immunology
  • Hepatitis B, Chronic / virology
  • Hepatocytes / drug effects*
  • Hepatocytes / immunology
  • Hepatocytes / virology
  • Host-Pathogen Interactions
  • Humans
  • Interferon-gamma / genetics
  • Interferon-gamma / immunology
  • Interleukin-10 / genetics
  • Interleukin-10 / immunology
  • Interleukins / genetics
  • Interleukins / immunology
  • Interleukins / pharmacology*
  • Leukocytes, Mononuclear / drug effects*
  • Leukocytes, Mononuclear / immunology
  • Leukocytes, Mononuclear / virology
  • Primary Cell Culture
  • Recombinant Proteins / pharmacology
  • Signal Transduction
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / immunology
  • Virus Replication / drug effects*

Substances

  • DNA, Viral
  • IL10 protein, human
  • Interleukins
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • Interferon-gamma
  • interleukin-21