儿童特应性皮炎、变应性鼻炎和支气管哮喘的标志物:与聚丝蛋白、嗜酸性粒细胞主要碱性蛋白和免疫球蛋白E的相关性

Q2 Medicine
Clinical and Molecular Allergy Pub Date : 2018-11-12 eCollection Date: 2018-01-01 DOI:10.1186/s12948-018-0102-y
Zafar Rasheed, Khaled Zedan, Ghada Bin Saif, Ragaa H Salama, Tarek Salem, Ahmed A Ahmed, Alaa Abd El-Moniem, Maha Elkholy, Ahmad A Al Robaee, Abdullateef A Alzolibani
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引用次数: 19

摘要

背景:过敏反应与许多特应性疾病有关,包括特应性皮炎(AD)、过敏性鼻炎(AR)和支气管哮喘(BA)。然而,聚丝蛋白、嗜酸性粒细胞主要碱性蛋白(MBP)和免疫球蛋白E (IgE)在儿科患者中引发过敏反应或导致特应性疾病的可能性仍未得到充分研究。本研究旨在探讨聚丝蛋白、嗜酸性粒细胞MBP和总IgE在儿童AD、AR和BA患者中的地位及其作用。方法:对395例AD、AR或BA患儿(根据疾病活动性指数)和410例年龄匹配的非特应性健康对照进行血清特应性标志物水平的评估,包括聚丝蛋白、嗜酸性粒细胞MBP和IgE。结果:血清分析显示,聚丝蛋白水平在儿童AD患者中显著高,其次是BA和AR,而在非特应性儿童对照组中其水平较低。特异应性患者血清中嗜酸性粒细胞MBP水平明显高于各自的对照组,但其水平在AR患者中最高,其次是AD和BA。AD患者血清中的总IgE水平明显高,其次是AR和BA患者,而非特应性儿童对照组的总IgE水平较低。有趣的是,不仅聚丝蛋白、嗜酸性粒细胞MBP或总IgE阳性的受试者数量增加,而且疾病活动性评分较高的特应性患者的水平也明显高于疾病活动性评分较低的特应性患者。结论:这些发现有力地支持聚丝蛋白、嗜酸性粒细胞MBP和IgE在儿童AD、AR和BA患者过敏反应发生中的作用。这些数据表明,聚丝蛋白、嗜酸性粒细胞MBP或IgE可能有助于评估AD、AR或BA的进展,并有助于阐明这些儿童疾病的发病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Markers of atopic dermatitis, allergic rhinitis and bronchial asthma in pediatric patients: correlation with filaggrin, eosinophil major basic protein and immunoglobulin E.

Markers of atopic dermatitis, allergic rhinitis and bronchial asthma in pediatric patients: correlation with filaggrin, eosinophil major basic protein and immunoglobulin E.

Markers of atopic dermatitis, allergic rhinitis and bronchial asthma in pediatric patients: correlation with filaggrin, eosinophil major basic protein and immunoglobulin E.

Markers of atopic dermatitis, allergic rhinitis and bronchial asthma in pediatric patients: correlation with filaggrin, eosinophil major basic protein and immunoglobulin E.

Background: Allergic reactions have been implicated as contributions in a number of atopic disorders, including atopic dermatitis (AD), allergic rhinitis (AR) and bronchial asthma (BA). However, the potential for filaggrin protein, eosinophil major basic protein (MBP) and immunoglobulin E (IgE) to elicit allergic response or to contribute to atopic disorders remains largely unexplored in pediatric patients. This study was undertaken to investigate the status and contribution of filaggrin protein, eosinophil MBP and total IgE in pediatric patients with AD, AR and BA.

Methods: Sera from 395 pediatric patients of AD, AR or BA with varying levels of disease activity according to the disease activity index and 410 age-matched non-atopic healthy controls were evaluated for serum levels of atopic markers, including filaggrin, eosinophil MBP and IgE.

Results: Serum analysis showed that filaggrin levels were remarkably high in pediatric patients with AD, followed by BA and AR, whereas its levels were low in non-atopic pediatric controls. Eosinophil MBP levels in sera of atopic patients were significantly high as compared with their respective controls, but its levels were highest in AR patients, followed by AD and BA. Total IgE in sera of AD patients was markedly high, followed by AR and BA patients, whereas its levels were low in non-atopic pediatric controls. Interestingly, not only was an increased number of subjects positive for filaggrin protein, eosinophil MBP or total IgE, but also their levels were statistically significantly higher among those atopic patients whose disease activity scores were higher as compared with atopic patients with lower disease activity scores.

Conclusions: These findings strongly support a role of filaggrin protein, eosinophil MBP and IgE in the onset of allergic reactions in pediatric patients with AD, AR and BA. The data suggest that filaggrin, eosinophil MBP or IgE might be useful in evaluating the progression of AD, AR or BA and in elucidating the mechanisms involved in the pathogenesis of these pediatric disorders.

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来源期刊
Clinical and Molecular Allergy
Clinical and Molecular Allergy Medicine-Immunology and Allergy
CiteScore
8.20
自引率
0.00%
发文量
11
审稿时长
13 weeks
期刊介绍: Clinical and Molecular Allergy is an open access, peer-reviewed, online journal that publishes research on human allergic and immunodeficient disease (immune deficiency not related to HIV infection/AIDS). The scope of the journal encompasses all aspects of the clinical, genetic, molecular and inflammatory aspects of allergic-respiratory (Type 1 hypersensitivity) and non-AIDS immunodeficiency disorders. However, studies of allergic/hypersensitive aspects of HIV infection/AIDS or drug desensitization protocols in AIDS are acceptable. At the basic science level, this includes original work and reviews on the genetic and molecular mechanisms underlying the inflammatory response.
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