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基于小儿食管黏液中嗜酸粒细胞阳离子蛋白肽配体对嗜酸性粒细胞性食管炎的辅助诊断。

Eosinophilic esophagitis auxiliary diagnosis based on a peptide ligand to eosinophil cationic protein in esophageal mucus of pediatric patients.

机构信息

Laboratory of Nanobiotechnology Prof. Dr. Luiz Ricardo Goulart Filho, Institute of Biotechnology, Federal University of Uberlandia, Uberlandia, MG, Brazil.

Pediatric Department, Federal University of Uberlandia, Uberlandia, MG, Brazil.

出版信息

Sci Rep. 2022 Jul 18;12(1):12226. doi: 10.1038/s41598-022-16293-1.

Abstract

Eosinophilic esophagitis (EoE) is a chronic inflammatory condition of the esophagus characterized by increased number of eosinophils. Currently, EoE diagnosis is based on endoscopic procedures for histopathological examination, eosinophils' counting and, often, in clinical practice, the challenge is the differentiation between EoE and gastroesophageal reflux disease (GERD). Our aim was to develop novel peptide ligand to Eosinophil cationic protein (ECP) present in EoE biopsies of patients with potential to be used for detection. We performed a comparative proteomic analysis using liquid chromatography-tandem mass spectrometry (LC-MS/MS) of esophageal biopsies from pediatric patients with eosinophilic esophagitis, gastroesophageal reflux disease and control individuals. Then, phage display technology was used to select peptides against specific up-regulated protein from EoE patients. Twelve phage clones were selected after three biopanning rounds, and the best phage clone reactivity was evaluated by phage-ELISA assay using esophageal mucus samples from 94 pediatric patients. Mass spectrometry showed that eosinophil cationic protein (ECP) was one of the most up-regulated proteins in EoE patients, which is an eosinophil granule protein usually deposited on tissues to mediate remodeling, but in excess may cause fibrosis and hypertrophy, especially in allergic responses. A highly reactive ECP-ligand peptide (E5) was able to distinguish reactive mucus of EoE patients from GERD and the control individuals by Phage-ELISA, achieving a sensitivity of 84.62%, and a specificity of 82.72%. This is the first study that successfully demonstrated an antibody-like peptide targeting ECP at the esophagus mucus as a useful auxilliary tool for EoE diagnosis with a significant association with atopic disorders and dysphagia.ClinicalTrials.gov no.: NCT03069573.

摘要

嗜酸性食管炎(EoE)是一种以食管中嗜酸性粒细胞增多为特征的慢性炎症性疾病。目前,EoE 的诊断基于内镜检查进行组织病理学检查、嗜酸性粒细胞计数,并且在临床实践中,通常的挑战是区分 EoE 和胃食管反流病(GERD)。我们的目标是开发针对嗜酸性粒细胞阳离子蛋白(ECP)的新型肽配体,该蛋白存在于 EoE 患者的活检组织中,具有用于检测的潜力。我们使用液相色谱-串联质谱(LC-MS/MS)对患有嗜酸性食管炎、胃食管反流病和对照组的儿科患者的食管活检组织进行了比较蛋白质组学分析。然后,使用噬菌体展示技术从 EoE 患者中选择针对特定上调蛋白的肽。经过三轮生物淘选,共选择了 12 个噬菌体克隆,并用 94 名儿科患者的食管黏液样本通过噬菌体-ELISA 试验评估最佳噬菌体克隆的反应性。质谱分析显示,嗜酸性粒细胞阳离子蛋白(ECP)是 EoE 患者中上调最明显的蛋白之一,这是一种嗜酸性粒细胞颗粒蛋白,通常沉积在组织上以介导重塑,但过量可能导致纤维化和肥大,尤其是在过敏反应中。通过噬菌体-ELISA,能够区分 EoE 患者的反应性黏液与 GERD 和对照组,高反应性 ECP 配体肽(E5)的敏感性为 84.62%,特异性为 82.72%。这是第一项成功证明靶向食管黏液中 ECP 的抗体样肽作为 EoE 诊断的有用辅助工具的研究,与特应性疾病和吞咽困难有显著关联。临床试验编号:NCT03069573。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/660a/9293922/29ea744c19be/41598_2022_16293_Fig1_HTML.jpg

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