Abstract
Development of an effective vaccine against the hepatitis C virus (HCV) has long been defined as a difficult challenge due to the considerable variability of this RNA virus and the observation that convalescent humans and chimpanzees could be re-infected after re-exposure. On the other hand, progress in the understanding of antiviral immune responses in patients with viral clearance has elucidated key mechanisms playing a role in the control of viral infection. Studies investigating prophylactic vaccine approaches in chimpanzees have confirmed that the induction and maintenance of strong helper and cytotoxic T-cell immune responses against multiple viral epitopes is necessary for protection against viral clearance and chronic infection. A multispecific B-cell response, resulting in rapid induction of cross-neutralizing antibodies may assist cellular responses. Therapeutic vaccine formulations currently being evaluated in clinical trials are facing the fact that the immune system of chronic carriers is impaired and needs the restoration of T-cell functions to enhance their efficacy.
Financial & competing interests disclosure
This work was supported by Inserm, France, Université Louis Pasteur de Strasbourg (CONECTUS), France, Hôpitaux Universitaires de Strasbourg, France, the European Union (LSHM-CT-2004-503359), the chair of excellence program of the Agence Nationale de la Recherche (ANR-05-CEXC-008), France, the Agence Nationale de la Recherche sur le SIDA et les Hépatites Virales (ANRS-06221), France, the Else-Kröner-Fresenius Foundation, Bad Homburg (P17/07//A83/06), Germany and the Deutsche Forschungsgemeinschaft (Ba3643/1-1; Ba1417/11-2), Bonn, Germany. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.
No writing assistance was utilized in the production of this manuscript.