Titel
Accueil
Navigation principale
Contenu
Recherche
Aide
Fonte
Standard
Gras
Identifiant
Interrompre la session?
Une session sous le nom de
InternetUser
est en cours.
Souhaitez-vous vraiment vous déconnecter?
Interrompre la session?
Une session sous le nom de
InternetUser
est en cours.
Souhaitez-vous vraiment vous déconnecter?
Accueil
Plus de données
Partenaires
Aide
Mentions légales
D
F
E
La recherche est en cours.
Interrompre la recherche
Recherche de projets
Projet actuel
Projets récents
Graphiques
Identifiant
Titel
Titel
Unité de recherche
PCRD EU
Numéro de projet
99.0365
Titre du projet
HCVACC-COIM: B1 - immune correlates of protection and chronicity in hepatitis c virus infection
Titre du projet anglais
HCVACC-COIM: B1 - immune correlates of protection and chronicity in hepatitis c virus infection
Données de base
Textes
Participants
Titel
Textes relatifs à ce projet
Allemand
Français
Italien
Anglais
Mots-clé
-
-
-
Autre Numéro de projet
-
-
-
Programme de recherche
-
-
-
Description succincte
-
-
-
Partenaires et organisations internationales
-
-
-
Résumé des résultats (Abstract)
-
-
-
Références bases de données
-
-
-
Textes saisis
Catégorie
Texte
Mots-clé
(Anglais)
Hepatitis C; protective immunity; vaccine development; induction of cellular immunity; therapeutic vaccine
Autre Numéro de projet
(Anglais)
EU project number: QLK2-1999-00356
Programme de recherche
(Anglais)
EU-programme: 5. Frame Research Programme - 1.1.2 Control of infectious diseases
Description succincte
(Anglais)
See abstract
Partenaires et organisations internationales
(Anglais)
Coordinator: LMU-München (D)
Résumé des résultats (Abstract)
(Anglais)
It is the overall objective of this cluster to contribute to the development of preventive and therapeutic vaccines against hepatitis C virus infection. Within this project, the immune response during natural infection with HCV in patients with different courses of infection shall be studied. The emphasis will be on those aspects of the immune response which are of direct relevance for the development of vaccines and the monitoring of vaccine success.
New techniques for the characterisation of virusspecific T cells and virus-neutralising antibodies, which have only recently become available, are employed to characterise (i) naturally occurring immune mechanisms that are associated with viral clearance and immunity; (ii) immunoregulatory and viral factors leading to viral persistence which may interfere with the induction of a protective immune response; (iii) the antiviral immune response during chronic HCV infection which is unable to clear the infection but will be interacting with attempts at the induction of protective immune responses. Although considerable work has been done on the HCV specific immune response during the last several years, the relevance of neutralising antibodies and HCV-specific cytotoxic T cells is still poorly understood. Due to the difficulties in defining CD8+ T cell epitopes it is presently not known whether important CTL epitopes can be studied in a given patient and this is one reason why the impact of viral mutations on the outcome of HCV infection is still debated.
During the last year, several new immunological techniques have revolutionised the field of viral immunology. Apart from classical tests we are using a new technique, the enzyme linked immunospot (Elispot) which allows the detection of specific cytokine secretion at a single cell level. This assay has been successfully adapted for characterisation of both virus specific DC4+ as wells as CD8+ T cells.
Our group is focusing on the identification of new CD8+ T cell eptitopes and definition of their relative immunodominance as well as on the clarification of the contribution of virus specific CD8+ T lymphocytes for viral clearance in acute hepatitis C.
Références bases de données
(Anglais)
Swiss Database: Euro-DB of the
State Secretariat for Education and Research
Hallwylstrasse 4
CH-3003 Berne, Switzerland
Tel. +41 31 322 74 82
Swiss Project-Number: 99.0365
SEFRI
- Einsteinstrasse 2 - 3003 Berne -
Mentions légales