Project IP-CURE-B

Belgium France Germany Italy Spain United States

Project ongoing

ipcureb.eu

Short description

Development of new curative concepts for chronic hepatitis B based on the remodelling of intrahepatic immune responses

Domains

  • Research

Themes

  • Communicable diseases

Sub-themes

  • Modelling response to treatment against HBV, support for a clinical trial.
  • SISTM is involved in modelling the immune response to treatment and MART/EUCLID is involved in organising the clinical trial.

Countries

  • Belgium
  • France
  • Germany
  • Italy
  • Spain
  • United States

Participating teams in Bordeaux

MART/EUCLID SISTM

Partner institutions in France

International partner institutions

Activity summary

The aim of the IP-CURE-B project is to develop new curative concepts for chronic hepatitis B based on the remodelling of intrahepatic immune responses. The consortium of 14 partners is also working on a preclinical immune therapy platform, a proof-of-concept clinical trial and virological and immune profiling of patients to improve treatment follow-up.

The project will aim to :
• Carrying out a clinical proof of concept to evaluate new immunomodulatory strategies aimed at strengthening innate immunity and remodelling the immune environment in the infected liver with a view to improving adaptive immunity and responding better to stimulation by a therapeutic vaccine.
• Characterising biomarkers and immune and viral signatures in clinically relevant cohorts, which will then be used to stratify patients for treatment and monitor responses to host-targeted therapies.
• Design, produce and select the best DNA replicon-based (DREP) and dendritic cell (DC)-targeted HBC vaccines and their combinations. They will be evaluated in the HIS- HUHEP double-humanised mouse model, with the same innate immunity enhancement, before moving on to evaluation in clinical trials.
• Carrying out a clinical proof of concept to evaluate new immunomodulatory strategies aimed at strengthening innate immunity and remodelling the immune environment in the infected liver with a view to improving adaptive immunity and responding better to stimulation by a therapeutic vaccine.
• Characterising biomarkers and immune and viral signatures in clinically relevant cohorts, which will then be used to stratify patients for treatment and monitor responses to host-targeted therapies.
• Design, produce and select the best DNA replicon-based (DREP) and dendritic cell (DC)-targeted HBC vaccines and their combinations. They will be evaluated in the HIS- HUHEP double-humanised mouse model, with the same innate immunity enhancement, before moving on to evaluation in clinical trials.

Project contacts

Melanie Prague
Melanie.prague@u-bordeaux.fr

Linda Wittkop
linda.wittkop@u-bordeaux.fr

Anton Ottavi
anton.ottavi@u-bordeaux.fr

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