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Type 2 Inflammation in Eosinophilic Esophagitis: From Pathophysiology to Therapeutic Targets

Eosinophilic esophagitis (EoE) is a chronic immune-mediated disease of the esophagus characterized clinically by symptoms related to esophageal dysfunction and histologically by eosinophil-predominant inflammation, whose incidence is rising. It significantly affects patients’ quality of life and, if...

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Autores principales: Racca, Francesca, Pellegatta, Gaia, Cataldo, Giuseppe, Vespa, Edoardo, Carlani, Elisa, Pelaia, Corrado, Paoletti, Giovanni, Messina, Maria Rita, Nappi, Emanuele, Canonica, Giorgio Walter, Repici, Alessandro, Heffler, Enrico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790151/
https://www.ncbi.nlm.nih.gov/pubmed/35095572
http://dx.doi.org/10.3389/fphys.2021.815842
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author Racca, Francesca
Pellegatta, Gaia
Cataldo, Giuseppe
Vespa, Edoardo
Carlani, Elisa
Pelaia, Corrado
Paoletti, Giovanni
Messina, Maria Rita
Nappi, Emanuele
Canonica, Giorgio Walter
Repici, Alessandro
Heffler, Enrico
author_facet Racca, Francesca
Pellegatta, Gaia
Cataldo, Giuseppe
Vespa, Edoardo
Carlani, Elisa
Pelaia, Corrado
Paoletti, Giovanni
Messina, Maria Rita
Nappi, Emanuele
Canonica, Giorgio Walter
Repici, Alessandro
Heffler, Enrico
author_sort Racca, Francesca
collection PubMed
description Eosinophilic esophagitis (EoE) is a chronic immune-mediated disease of the esophagus characterized clinically by symptoms related to esophageal dysfunction and histologically by eosinophil-predominant inflammation, whose incidence is rising. It significantly affects patients’ quality of life and, if left untreated, results in fibrotic complications. Although broad consensus has been achieved on first-line therapy, a subset of patients remains non-responder to standard therapy. The pathogenesis of EoE is multifactorial and results from the complex, still mostly undefined, interaction between genetics and intrinsic factors, environment, and antigenic stimuli. A deep understanding of the pathophysiology of this disease is pivotal for the development of new therapies. This review provides a comprehensive description of the pathophysiology of EoE, starting from major pathogenic mechanisms (genetics, type 2 inflammation, epithelial barrier dysfunction, gastroesophageal reflux, allergens, infections and microbiota) and subsequently focusing on the single protagonists of type 2 inflammation (involved cells, cytokines, soluble effectors, surface proteins and transcription factors) that could represent present and future therapeutic targets, while summarizing previous therapeutic approaches in literature.
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spelling pubmed-87901512022-01-27 Type 2 Inflammation in Eosinophilic Esophagitis: From Pathophysiology to Therapeutic Targets Racca, Francesca Pellegatta, Gaia Cataldo, Giuseppe Vespa, Edoardo Carlani, Elisa Pelaia, Corrado Paoletti, Giovanni Messina, Maria Rita Nappi, Emanuele Canonica, Giorgio Walter Repici, Alessandro Heffler, Enrico Front Physiol Physiology Eosinophilic esophagitis (EoE) is a chronic immune-mediated disease of the esophagus characterized clinically by symptoms related to esophageal dysfunction and histologically by eosinophil-predominant inflammation, whose incidence is rising. It significantly affects patients’ quality of life and, if left untreated, results in fibrotic complications. Although broad consensus has been achieved on first-line therapy, a subset of patients remains non-responder to standard therapy. The pathogenesis of EoE is multifactorial and results from the complex, still mostly undefined, interaction between genetics and intrinsic factors, environment, and antigenic stimuli. A deep understanding of the pathophysiology of this disease is pivotal for the development of new therapies. This review provides a comprehensive description of the pathophysiology of EoE, starting from major pathogenic mechanisms (genetics, type 2 inflammation, epithelial barrier dysfunction, gastroesophageal reflux, allergens, infections and microbiota) and subsequently focusing on the single protagonists of type 2 inflammation (involved cells, cytokines, soluble effectors, surface proteins and transcription factors) that could represent present and future therapeutic targets, while summarizing previous therapeutic approaches in literature. Frontiers Media S.A. 2022-01-12 /pmc/articles/PMC8790151/ /pubmed/35095572 http://dx.doi.org/10.3389/fphys.2021.815842 Text en Copyright © 2022 Racca, Pellegatta, Cataldo, Vespa, Carlani, Pelaia, Paoletti, Messina, Nappi, Canonica, Repici and Heffler. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Racca, Francesca
Pellegatta, Gaia
Cataldo, Giuseppe
Vespa, Edoardo
Carlani, Elisa
Pelaia, Corrado
Paoletti, Giovanni
Messina, Maria Rita
Nappi, Emanuele
Canonica, Giorgio Walter
Repici, Alessandro
Heffler, Enrico
Type 2 Inflammation in Eosinophilic Esophagitis: From Pathophysiology to Therapeutic Targets
title Type 2 Inflammation in Eosinophilic Esophagitis: From Pathophysiology to Therapeutic Targets
title_full Type 2 Inflammation in Eosinophilic Esophagitis: From Pathophysiology to Therapeutic Targets
title_fullStr Type 2 Inflammation in Eosinophilic Esophagitis: From Pathophysiology to Therapeutic Targets
title_full_unstemmed Type 2 Inflammation in Eosinophilic Esophagitis: From Pathophysiology to Therapeutic Targets
title_short Type 2 Inflammation in Eosinophilic Esophagitis: From Pathophysiology to Therapeutic Targets
title_sort type 2 inflammation in eosinophilic esophagitis: from pathophysiology to therapeutic targets
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790151/
https://www.ncbi.nlm.nih.gov/pubmed/35095572
http://dx.doi.org/10.3389/fphys.2021.815842
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