New perspectives in eosinophilic granulomatosis ...
Type de document :
Article dans une revue scientifique: Article original
PMID :
URL permanente :
Titre :
New perspectives in eosinophilic granulomatosis with polyangiitis (egpa): report of the first meeting of the european egpa study group
Auteur(s) :
Marvisi, Chiara [Auteur]
Sinico, Renato Alberto [Auteur]
Salvarani, Carlo [Auteur]
Jayne, David [Auteur]
Prisco, Domenico [Auteur]
Terrier, Benjamin [Auteur]
Emmi, Giacomo [Auteur]
Vaglio, Augusto [Auteur]
Sinico, Renato Alberto [Auteur]
Salvarani, Carlo [Auteur]
Jayne, David [Auteur]
Prisco, Domenico [Auteur]
Terrier, Benjamin [Auteur]
Emmi, Giacomo [Auteur]
Vaglio, Augusto [Auteur]
Titre de la revue :
Internal and Emergency Medicine
Nom court de la revue :
Intern Emerg Med
Date de publication :
2019-08-06
ISSN :
1970-9366
Mot(s)-clé(s) en anglais :
ANCA
Mepolizumab
Rituximab
Vasculitis
Eosinophils
Eosinophilic granulomatosis with polyangiitis
Mepolizumab
Rituximab
Vasculitis
Eosinophils
Eosinophilic granulomatosis with polyangiitis
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
The European Eosinophilic Granulomatosis with Polyangiitis (EGPA) study group first gathered in Firenze in December 2018. The discussion was centred around the clinical and therapeutic needs in EGPA which still remain ...
Lire la suite >The European Eosinophilic Granulomatosis with Polyangiitis (EGPA) study group first gathered in Firenze in December 2018. The discussion was centred around the clinical and therapeutic needs in EGPA which still remain unmet. Indeed, EGPA is a puzzling and rare disease which shares clinical features with other anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAVs) and hypereosinophilic syndromes (HESs). Some of the recommendations published in 2015 are based on data derived from EGPA-related diseases, rather than from EGPA itself, and therefore need to be updated. Thus, the aim of the meeting was to stimulate ongoing research, to promote collaborative European studies and to define the main issues on which future studies should be focused. Current fields of research on EGPA include potential serological biomarkers of disease activity and of specific organ involvement, possible links between different genetic variants and clinical phenotypes, and new therapeutic perspectives. Herein, we give an overview of the meeting with the goal to stimulate an international collaboration and new points of discussion.Lire moins >
Lire la suite >The European Eosinophilic Granulomatosis with Polyangiitis (EGPA) study group first gathered in Firenze in December 2018. The discussion was centred around the clinical and therapeutic needs in EGPA which still remain unmet. Indeed, EGPA is a puzzling and rare disease which shares clinical features with other anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAVs) and hypereosinophilic syndromes (HESs). Some of the recommendations published in 2015 are based on data derived from EGPA-related diseases, rather than from EGPA itself, and therefore need to be updated. Thus, the aim of the meeting was to stimulate ongoing research, to promote collaborative European studies and to define the main issues on which future studies should be focused. Current fields of research on EGPA include potential serological biomarkers of disease activity and of specific organ involvement, possible links between different genetic variants and clinical phenotypes, and new therapeutic perspectives. Herein, we give an overview of the meeting with the goal to stimulate an international collaboration and new points of discussion.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Date de dépôt :
2024-01-30T10:28:02Z