Coexisting inflammatory bowel disease and eosinophilic esophagitis: moving beyond parallel narratives to an integrated framework.

IF 4 3区 医学 Q2 IMMUNOLOGY
Expert Review of Clinical Immunology Pub Date : 2026-08-01 Epub Date: 2026-08-31 DOI:10.1080/1744666X.2026.2725811
Chidera Onwuzo, Cynthia Okonkwo, Gaurav Chauhan, Idan Goren
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引用次数: 0

Abstract

Introduction: Eosinophilic esophagitis (EoE) and inflammatory bowel disease (IBD) are chronic immune-mediated gastrointestinal disorders traditionally framed as biologically distinct, yet epidemiologic data increasingly support a bidirectional association.

Areas covered: This narrative review examines the epidemiology,immunopathogenesis, and clinical implications of coexisting EoE and IBD using a targeted PubMed search through 2025 with reference-list screening. Although EoE is classically driven by type 2 inflammation and IBD by Th1/Th17 pathways, both disorders converge on epithelial barrier injury, innate immune dysregulation, and fibroblast-mediated remodeling. These shared downstream mechanisms may help explain diagnostic overshadowing, treatment resistance, and an increased propensity for fibrostenotic complications in patients with dual disease.

Expert opinion: Coexisting EoE and IBD may be better viewed less as a chance overlap and more as a potentially meaningful clinical association. A mechanism-based approach that incorporates risk enrichment, early endoscopic evaluation, nutritional comanagement, and therapies directed at shared inflammatory-fibrotic pathways may improve outcomes. Future progress will depend on prospective cohorts, biomarker development, and trials that intentionally include patients with both conditions.

共存的炎症性肠病和嗜酸性粒细胞性食管炎:超越平行叙事到一个综合框架
嗜酸性粒细胞性食管炎(EoE)和炎症性肠病(IBD)是慢性免疫介导的胃肠道疾病,传统上被认为是生物学上不同的,但流行病学数据越来越多地支持两者之间的双向关联。涵盖领域:本综述通过PubMed检索,通过参考文献列表筛选,研究了2025年之前EoE和IBD共存的流行病学、免疫发病机制和临床意义。虽然EoE通常由2型炎症和IBD通过Th1/Th17途径驱动,但这两种疾病都集中在上皮屏障损伤、先天免疫失调和成纤维细胞介导的重塑上。这些共同的下游机制可能有助于解释双重疾病患者的诊断掩盖、治疗抵抗和纤维狭窄并发症的增加倾向。专家意见:共存的EoE和IBD可能更少被视为偶然的重叠,而更多地被视为潜在的有意义的临床关联。一种基于机制的方法,结合风险富集、早期内窥镜评估、营养管理和针对共同炎症-纤维化途径的治疗,可能会改善结果。未来的进展将取决于前瞻性队列、生物标志物的发展,以及有意纳入两种情况患者的试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.60
自引率
2.30%
发文量
221
审稿时长
6-12 weeks
期刊介绍: Expert Review of Clinical Immunology (ISSN 1744-666X) provides expert analysis and commentary regarding the performance of new therapeutic and diagnostic modalities in clinical immunology. Members of the International Editorial Advisory Panel of Expert Review of Clinical Immunology are the forefront of their area of expertise. This panel works with our dedicated editorial team to identify the most important and topical review themes and the corresponding expert(s) most appropriate to provide commentary and analysis. All articles are subject to rigorous peer-review, and the finished reviews provide an essential contribution to decision-making in clinical immunology. Articles focus on the following key areas: • Therapeutic overviews of specific immunologic disorders highlighting optimal therapy and prospects for new medicines • Performance and benefits of newly approved therapeutic agents • New diagnostic approaches • Screening and patient stratification • Pharmacoeconomic studies • New therapeutic indications for existing therapies • Adverse effects, occurrence and reduction • Prospects for medicines in late-stage trials approaching regulatory approval • Novel treatment strategies • Epidemiological studies • Commentary and comparison of treatment guidelines Topics include infection and immunity, inflammation, host defense mechanisms, congenital and acquired immunodeficiencies, anaphylaxis and allergy, systemic immune diseases, organ-specific inflammatory diseases, transplantation immunology, endocrinology and diabetes, cancer immunology, neuroimmunology and hematological diseases.
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