Examining the Role of Type 2 Inflammation in Eosinophilic Esophagitis.

Endotypes Eosinophilic Esophagitis Eosinophils Type 2 Inflammation

Journal

Gastro hep advances
ISSN: 2772-5723
Titre abrégé: Gastro Hep Adv
Pays: Netherlands
ID NLM: 9918350485906676

Informations de publication

Date de publication:
2022
Historique:
received: 15 12 2021
accepted: 06 05 2022
medline: 21 5 2022
pubmed: 21 5 2022
entrez: 12 8 2024
Statut: epublish

Résumé

Eosinophilic esophagitis (EoE) is a chronic type 2 inflammatory disease characterized by an eosinophilic inflammatory infiltrate in the esophagus, leading to remodeling, stricture formation, and fibrosis. Triggered by food and aeroallergens, type 2 cytokines interleukin (IL)-4, IL-13, IL-5 produced by CD4+ T helper 2 cells (Th2), eosinophils, mast cells, basophils, and type 2 innate lymphoid cells alter the esophageal epithelial barrier and increase inflammatory cell tissue infiltration. Clustering analysis based on the expression of type 2 inflammatory genes demonstrated the diversity of EoE endotypes. Despite the availability of treatment options for patients with EoE, which include dietary restriction, proton pump inhibitors, swallowed topical steroids, and esophageal dilation, there are still no Food and Drug Administration-approved medications for this disease; as such, there are clear unmet medical needs for these patients. A number of novel biologic therapies currently in clinical trials represent a promising avenue for targeted therapeutic approaches in EoE. This review summarizes our current knowledge on the role of type 2 inflammatory cells and mediators in EoE disease pathogenesis, as well as the future treatment landscape targeting underlying inflammation in EoE.

Identifiants

pubmed: 39131849
doi: 10.1016/j.gastha.2022.05.004
pii: S2772-5723(22)00082-6
pmc: PMC11307682
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

720-732

Informations de copyright

© 2022 The Authors.

Auteurs

Mirna Chehade (M)

Deparment of Pediatrics and Medicine, Mount Sinai Center for Eosinophilic Disorders, Icahn School of Medicine at Mount Sinai, New York, New York.

Gary W Falk (GW)

Division of Gastroenterology, Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.

Seema Aceves (S)

Deparment of Pediatrics and Medicine, University of California, San Diego, California.

Jason K Lee (JK)

Deparment of Clinical Immunology and Allergy and Internal Medicine, Toronto Allergy and Asthma Clinic, Toronto, Ontario, Canada.

Vinay Mehta (V)

Allergy, Asthma & Immunology Associates, P.C., Lincoln, Nebraska.

John Leung (J)

Boston Specialists, Boston, Massachusetts.

Brad Shumel (B)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York.

Juby A Jacob-Nara (JA)

Sanofi, Bridgewater, New Jersey.

Yamo Deniz (Y)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York.

Paul J Rowe (PJ)

Sanofi, Bridgewater, New Jersey.

Danen Cunoosamy (D)

Sanofi, Cambridge, Massachusetts.

Angela Khodzhayev (A)

Regeneron Pharmaceuticals, Inc, Tarrytown, New York.

Classifications MeSH