Cell Culture Models for Hepatitis B and D Viruses Infection: Old Challenges, New Developments and Future Strategies

Arnaud Carpentier1,2,3

  • 1Institute for Experimental Virology, TWINCORE Centre for Experimental and Clinical Infection Research, a Joint Venture between Hannover Medical School (MHH) and Helmholtz Centre for Infection Research (HZI), Feodor-Lynen-Strasse 7, 30625 Hannover, Germany.

Viruses
|May 25, 2024
PubMed

Insights

Hepatitis B and D virus (HBV and HDV) co-infection causes severe liver disease with no cure. This review examines cell culture models to understand HBV and HDV interactions for developing new treatments.

Area of Science:

  • * Virology and Hepatology
  • * Viral pathogenesis and host-pathogen interactions

Background:

  • * Chronic Hepatitis B and D Virus (HBV and HDV) co-infection causes the most severe form of viral hepatitis, known as Hepatitis Delta.
  • * Despite an HBV vaccine, HBV/HDV co-infection remains a significant global health issue with no effective curative treatments.
  • * HBV and HDV share closely linked life cycles, with HDV depending on HBV for replication, making cellular responses to HDV impactful on HBV replication.

Purpose of the Study:

  • * To review available cell culture models for studying HBV and HDV infection and co-infection.
  • * To discuss the relevance of these models in understanding HBV and HDV virology and host-pathogen interactions.
  • * To highlight how these models can aid in developing new therapeutic strategies for viral clearance.

Main Methods:

  • * Comprehensive literature review of cell culture models used in HBV and HDV research.
  • * Analysis of the biological relevance and experimental amenability of different models.
  • * Discussion of model utility in studying viral replication and host responses.

Main Results:

  • * Various cell culture models exist for studying HBV and HDV, each with distinct advantages and limitations.
  • * Models differ significantly in their biological relevance and suitability for virological experiments.
  • * The choice of model impacts the ability to decipher viral mechanisms and host interactions.

Conclusions:

  • * Cell culture models are crucial tools for advancing the understanding of HBV and HDV.
  • * Evaluating model relevance is key to addressing remaining questions in HBV/HDV pathogenesis.
  • * Improved understanding through appropriate models is essential for developing effective therapies against HBV and HDV.