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

被引:36
|
作者
Racca, Francesca [1 ,2 ]
Pellegatta, Gaia [3 ]
Cataldo, Giuseppe [1 ]
Vespa, Edoardo [2 ,3 ]
Carlani, Elisa [3 ]
Pelaia, Corrado [4 ]
Paoletti, Giovanni [1 ,2 ]
Messina, Maria Rita [1 ,2 ]
Nappi, Emanuele [1 ,2 ]
Canonica, Giorgio Walter [1 ,2 ]
Repici, Alessandro [2 ,3 ]
Heffler, Enrico [1 ,2 ]
机构
[1] IRCCS Humanitas Res Hosp, Personalized Med Asthma & Allergy, Rozzano, Italy
[2] Humanitas Univ, Dept Biomed Sci, Pieve Emanuele, Italy
[3] IRCCS Humanitas Res Hosp, Dept Gastroenterol, Digest Endoscopy Unit, Rozzano, Italy
[4] Magna Graecia Univ Catanzaro, Dept Med & Surg Sci, Catanzaro, Italy
关键词
eosinophilic esophagitis; type; 2; inflammation; therapeutic targets; precision medicine; pathophysiology; THYMIC STROMAL LYMPHOPOIETIN; GENOME-WIDE ASSOCIATION; EPITHELIAL-MESENCHYMAL TRANSITION; DILATED INTERCELLULAR SPACES; ACTIVATED RECEPTOR-GAMMA; TOPICAL STEROID-THERAPY; INNATE LYMPHOID-CELLS; TGF-BETA ANTIBODY; QUALITY-OF-LIFE; GASTROESOPHAGEAL-REFLUX;
D O I
10.3389/fphys.2021.815842
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
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.
引用
收藏
页数:30
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