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嗜酸性食管炎的最新研究进展

Recent research advances in eosinophilic esophagitis.

作者信息

Oyoshi Michiko K

机构信息

Division of Immunology, Boston Children's Hospital and Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Curr Opin Pediatr. 2015 Dec;27(6):741-7. doi: 10.1097/MOP.0000000000000284.

DOI:10.1097/MOP.0000000000000284
PMID:26418324
Abstract

PURPOSE OF REVIEW

Eosinophilic esophagitis (EoE) is a chronic allergic disease triggered by food allergens with an increasing prevalence. This review highlights recent research advances in EoE with a focus on the literature of the past 18 months.

RECENT FINDINGS

The incidence of EoE in the black population is higher than previously suggested. A novel locus spanning CAPN14 is associated with EoE. Diagnostic tests utilizing an analysis of EoE-specific transcriptome have been improved. Standardized EoE symptom score systems have been established. Treatment trials show the promise and limitations of allergen avoidance, antiinflammatory reagents, and anti-interleukin-13 antibodies. Insights into disease mechanisms highlight the role of invariant natural killer T cells and group 2 innate immune cells. Epithelial barrier protein desmoglein 1, bone morphogenetic protein antagonist follistatin, neurotrophic tyrosine kinase receptor type 1, and CAPN14 have been defined as new potential therapeutic targets in EoE as regulators of the inflammatory interleukin-13-axis. The role of IgG4 in the disease mechanisms has been suggested.

SUMMARY

Genetic predisposition influenced by environmental factors increases EoE susceptibility. Research identifying the critical events leading to allergen sensitization and the esophagus-specific responses that drive EoE is evolving, and will lead to a better understanding of EoE and new therapeutic approaches for the disease.

摘要

综述目的

嗜酸性粒细胞性食管炎(EoE)是一种由食物过敏原引发的慢性过敏性疾病,其患病率呈上升趋势。本综述重点介绍了EoE的最新研究进展,尤其关注过去18个月的文献。

最新发现

黑人人群中EoE的发病率高于此前报道。一个跨越钙蛋白酶14(CAPN14)的新基因座与EoE相关。利用EoE特异性转录组分析的诊断测试得到了改进。已建立标准化的EoE症状评分系统。治疗试验显示了避免过敏原、抗炎试剂和抗白细胞介素-13抗体的前景和局限性。对疾病机制的深入了解突出了不变自然杀伤T细胞和2型固有免疫细胞的作用。上皮屏障蛋白桥粒芯糖蛋白1、骨形态发生蛋白拮抗剂卵泡抑素、神经营养性酪氨酸激酶受体1型和CAPN14已被确定为EoE中作为炎症白细胞介素-13轴调节剂的新潜在治疗靶点。已有人提出IgG4在疾病机制中的作用。

总结

受环境因素影响的遗传易感性增加了EoE的易感性。确定导致过敏原致敏的关键事件以及驱动EoE的食管特异性反应的研究正在不断发展,这将有助于更好地理解EoE并为该疾病带来新的治疗方法。

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1
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引用本文的文献

1
Genetics of eosinophilic esophagitis.嗜酸性粒细胞性食管炎的遗传学。
Mucosal Immunol. 2017 May;10(3):580-588. doi: 10.1038/mi.2017.4. Epub 2017 Feb 22.
2
Calpain-14 and its association with eosinophilic esophagitis.钙蛋白酶-14及其与嗜酸性粒细胞性食管炎的关联。
J Allergy Clin Immunol. 2017 Jun;139(6):1762-1771.e7. doi: 10.1016/j.jaci.2016.09.027. Epub 2017 Jan 25.
3
Eosinophilic esophagitis: published evidences for disease subtypes, indications for patient subpopulations, and how to translate patient observations to murine experimental models.
嗜酸性粒细胞性食管炎:疾病亚型的已发表证据、患者亚群的指征以及如何将患者观察结果转化为小鼠实验模型。
World Allergy Organ J. 2016 Jul 15;9:23. doi: 10.1186/s40413-016-0114-3. eCollection 2016.