AIC649 Induces a Bi-Phasic Treatment Response in the Woodchuck Model of Chronic Hepatitis B

PLoS One. 2015 Dec 14;10(12):e0144383. doi: 10.1371/journal.pone.0144383. eCollection 2015.

Abstract

AIC649 has been shown to directly address the antigen presenting cell arm of the host immune defense leading to a regulated cytokine release and activation of T cell responses. In the present study we analyzed the antiviral efficacy of AIC649 as well as its potential to induce functional cure in animal models for chronic hepatitis B. Hepatitis B virus transgenic mice and chronically woodchuck hepatitis virus (WHV) infected woodchucks were treated with AIC649, respectively. In the mouse system AIC649 decreased the hepatitis B virus titer as effective as the "gold standard", Tenofovir. Interestingly, AIC649-treated chronically WHV infected woodchucks displayed a bi-phasic pattern of response: The marker for functional cure--hepatitis surface antigen--first increased but subsequently decreased even after cessation of treatment to significantly reduced levels. We hypothesize that the observed bi-phasic response pattern to AIC649 treatment reflects a physiologically "concerted", reconstituted immune response against WHV and therefore may indicate a potential for inducing functional cure in HBV-infected patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents / therapeutic use*
  • Biological Therapy
  • Biomarkers / metabolism
  • Dendritic Cells / immunology
  • Disease Models, Animal
  • Hepatitis B Surface Antigens / metabolism*
  • Hepatitis B Virus, Woodchuck / immunology*
  • Hepatitis B virus / immunology
  • Hepatitis B, Chronic / drug therapy
  • Hepatitis B, Chronic / immunology*
  • Immunity, Cellular / immunology
  • Interferon-alpha / immunology
  • Interferon-gamma / immunology
  • Killer Cells, Natural / immunology
  • Lymphocyte Activation / immunology
  • Marmota / immunology*
  • Marmota / virology
  • Mice
  • Mice, Inbred BALB C
  • Mice, Transgenic
  • Parapoxvirus / immunology
  • T-Lymphocytes / immunology
  • Tenofovir / therapeutic use
  • Tumor Necrosis Factor-alpha / immunology
  • Tumor Necrosis Factor-alpha / metabolism
  • Vaccines, Inactivated / immunology
  • Virus Replication / drug effects

Substances

  • Antiviral Agents
  • Biomarkers
  • Hepatitis B Surface Antigens
  • Interferon-alpha
  • Tumor Necrosis Factor-alpha
  • Vaccines, Inactivated
  • Interferon-gamma
  • Tenofovir

Grants and funding

The work was financially supported by Bayer. DP and HRS are employees of AiCuris. OW is an employee of Bayer. AiCuris provided support in the form of salaries for authors DP and HRS, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. Bayer provided support in the form of salaries for authors OW, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.