Biologics in Hypereosinophilic Syndrome and Eosinophilic Granulomatosis with Polyangiitis.
Benralizumab
Biologic therapy
Dupilumab
Eosinophilia
Eosinophilic granulomatosis with polyangiitis
Hypereosinophilic syndrome
Mepolizumab
Reslizumab
Journal
Immunology and allergy clinics of North America
ISSN: 1557-8607
Titre abrégé: Immunol Allergy Clin North Am
Pays: United States
ID NLM: 8805635
Informations de publication
Date de publication:
Nov 2024
Nov 2024
Historique:
medline:
11
10
2024
pubmed:
11
10
2024
entrez:
10
10
2024
Statut:
ppublish
Résumé
Hypereosinophilic syndrome (HES) and eosinophilic granulomatosis with polyangiitis (EGPA) are complex disorders defined by blood and tissue eosinophilia and heterogeneous clinical manifestations. Historically, the mainstay of therapy for both conditions has been systemic glucocorticoids. However, recent availability of biologics that directly or indirectly target eosinophils has provided new avenues to pursue improved outcomes with decreased toxicity. In this article, we summarize the evidence supporting the use of specific biologics in HES and/or EGPA and provide a framework for their clinical use in patients.
Identifiants
pubmed: 39389714
pii: S0889-8561(24)00052-3
doi: 10.1016/j.iac.2024.07.003
pii:
doi:
Substances chimiques
Biological Products
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
629-644Subventions
Organisme : Intramural NIH HHS
ID : ZIA AI001130
Pays : United States
Informations de copyright
Published by Elsevier Inc.
Déclaration de conflit d'intérêts
Disclosure The authors have nothing to disclose. This work was supported in part by the Division of Intramural Research, NIAID, NIH.