Activated intrahepatic antigen-presenting cells inhibit hepatitis B virus replication in the liver of transgenic mice

J Immunol. 2002 Nov 1;169(9):5188-95. doi: 10.4049/jimmunol.169.9.5188.

Abstract

In this study we evaluated the ability of activated intrahepatic APCs to inhibit hepatitis B virus (HBV) replication in transgenic mice. Intrahepatic APCs were activated by administration of an anti-CD40 agonistic mAb (alphaCD40). We showed that a single i.v. injection of alphaCD40 was sufficient to inhibit HBV replication noncytopathically by a process associated with the recruitment of dendritic cells, macrophages, T cells, and NK cells into the liver and the induction of inflammatory cytokines. The antiviral effect depended on the production of IL-12 and TNF-alpha by activated APCs; however, it was mediated primarily by IFN-gamma produced by NK cells, and possibly T cells, that were activated by IL-12. Collectively, these results suggest that activated APCs can directly produce antiviral cytokines (IL-12, TNF-alpha) and trigger the production of other cytokines (i.e., IFN-gamma) by other cells (e.g., NK cells and T cells) that do not express CD40. These results provide insight into a hitherto unsuspected antiviral function of intrahepatic APCs, and they suggest that therapeutic activation of APCs may represent a new strategy for the treatment of chronic HBV infection.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / administration & dosage
  • Antigen-Presenting Cells / immunology*
  • Antigen-Presenting Cells / metabolism
  • Antigen-Presenting Cells / virology
  • Antiviral Agents / administration & dosage
  • CD40 Antigens / immunology
  • Cell Movement / immunology
  • Hepatitis B virus / immunology*
  • Hepatitis B virus / physiology
  • Inflammation / immunology
  • Inflammation / pathology
  • Injections, Intravenous
  • Interferon-gamma / physiology
  • Interleukin-12 / physiology
  • Liver / immunology*
  • Liver / metabolism
  • Liver / pathology
  • Liver / virology*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Transgenic
  • T-Lymphocytes / immunology
  • T-Lymphocytes / virology
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / physiology
  • Virus Replication / immunology*

Substances

  • Antibodies, Monoclonal
  • Antiviral Agents
  • CD40 Antigens
  • Tumor Necrosis Factor-alpha
  • Interleukin-12
  • Interferon-gamma