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嗜酸粒细胞性食管炎治疗的新治疗前沿:生物药物。

The New Therapeutic Frontiers in the Treatment of Eosinophilic Esophagitis: Biological Drugs.

机构信息

Department of Medicine and Surgery, University of Parma, 43121 Parma, Italy.

Departmental Unit of Allergology, Guglielmo da Saliceto Hospital, 29121 Piacenza, Italy.

出版信息

Int J Mol Sci. 2024 Jan 30;25(3):1702. doi: 10.3390/ijms25031702.

DOI:10.3390/ijms25031702
PMID:38338983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10855546/
Abstract

Eosinophilic esophagitis (EoE) is a multifaceted disease characterized by a wide heterogeneity of clinical manifestations, endoscopic and histopathologic patterns, and responsiveness to therapy. From the perspective of an effective approach to the patient, the different inflammatory mechanisms involved in the pathogenesis of EoE and biologics, in particular monoclonal antibodies (mAbs), targeting these pathways are needed. Currently, the most relevant is dupilumab, which interferes with both interleukin (IL)-4 and IL-13 pathways by binding IL-4 receptor α, and is the only mAb approved by the European Medicine Agency and US Food and Drug Administration for the treatment of EoE. Other mAbs investigated include mepolizumab, reslizumab, and benralizumab (interfering with IL-5 axis), cendakimab and dectrekumab (anti-IL-13s), tezepelumab (anti-TSLP), lirentelimab (anti-SIGLEG-8), and many others. Despite the undeniable economic impact of biologic therapies, in the near future, there will be room for further reflection about the opportunity to prescribe biologic agents, not only as a last-line therapy in selected cases such as patients with comorbidities involving common pathways. Although recent findings are very encouraging, the road to permanent success in the treatment of EoE is still long, and further studies are needed to determine the long-term effects of mAbs and to discover new potential targets.

摘要

嗜酸粒细胞性食管炎(EoE)是一种多方面的疾病,其临床表现、内镜和组织病理学模式以及对治疗的反应具有广泛的异质性。从对患者有效治疗的角度来看,需要针对 EoE 的发病机制和生物制剂(特别是靶向这些途径的单克隆抗体 [mAb])中涉及的不同炎症机制。目前,最相关的是度普利尤单抗,它通过结合白细胞介素(IL)-4 受体 α 来干扰 IL-4 和 IL-13 途径,是唯一一种获得欧洲药品管理局和美国食品和药物管理局批准用于治疗 EoE 的 mAb。其他正在研究的 mAb 包括美泊利单抗、瑞利珠单抗和贝那利珠单抗(干扰 IL-5 轴)、西仑单抗和德卡鲁单抗(抗 IL-13s)、替泽利珠单抗(抗 TSLP)、利仑替利单抗(抗 SIGLEG-8)和许多其他 mAb。尽管生物治疗的经济影响不可否认,但在不久的将来,对于是否有必要开生物制剂的处方,还需要进一步思考,不仅是在涉及共同途径的合并症等特定情况下作为二线治疗。尽管最近的发现非常令人鼓舞,但在 EoE 的治疗中取得永久成功的道路还很长,还需要进一步的研究来确定 mAb 的长期效果,并发现新的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6870/10855546/c01a626b0359/ijms-25-01702-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6870/10855546/c01a626b0359/ijms-25-01702-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6870/10855546/c01a626b0359/ijms-25-01702-g001.jpg

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Mechanistic Insights into Eosinophilic Esophagitis: Therapies Targeting Pathophysiological Mechanisms.嗜酸性粒细胞性食管炎的发病机制研究:针对病理生理机制的治疗方法。
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