Suppr超能文献

变应性支气管肺曲霉病的诊断仍然是一项挑战。

Allergic bronchopulmonary aspergillosis' diagnosis remains a challenge.

作者信息

de Oliveira Edilamara, Giavina-Bianchi Pedro, Fonseca Luiz Augusto Marcondes, França Alfeu Tavares, Kalil Jorge

机构信息

Division of Clinical Immunology and Allergy, University of São Paulo, R. Prof. Artur Ramos 178 ap.211A, 01454-904, São Paulo, SP, Brazil.

出版信息

Respir Med. 2007 Nov;101(11):2352-7. doi: 10.1016/j.rmed.2007.06.018. Epub 2007 Aug 3.

Abstract

INTRODUCTION

Allergic bronchopulmonary aspergillosis (ABPA) is a complex disease, triggered by a hypersensitivity reaction to the allergens of Aspergillus fumigatus, a fungus that opportunistically colonizes the lungs of patients with asthma. The diagnosis of ABPA is difficult. A major problem is the lack of standardized allergens used in the determination of specific IgE, but the use of recombinant allergens has been proposed to overcome this. The aim of the present study is to evaluate whether serological tests for IgE specific to recombinant allergens of A. fumigatus (rAsp) can aid in the detection of sensitization to this fungus and in the diagnosis of ABPA.

METHODS

This was an observational, cross-sectional study. The diagnosis of ABPA, using classical criteria, was searched in 65 asthmatics patients with immediate cutaneous reactivity to A. fumigatus. After that, serum titers of IgE against rAsp f 1, rAsp f 2, rAsp f 3, rAsp f 4 and rAsp f 6 were determined. In order to compare the differences between patients with confirmed and excluded diagnosis of ABPA, the two-tailed Fisher's exact test was used.

RESULTS

Although 19 of 65 patients had IgE against at least one recombinant, the disease was diagnosed in only six patients by classical criteria. One of them had IgE against all recombinant allergens tested and another one had antibody against Asp f 3.

DISCUSSION

The determination of serum IgE against recombinant A. fumigatus allergens in this group was not helpful to make the diagnosis of ABPA, neither to detect sensitization to fungus.

摘要

引言

变应性支气管肺曲霉病(ABPA)是一种复杂的疾病,由对烟曲霉过敏原的超敏反应引发,烟曲霉是一种机会性定植于哮喘患者肺部的真菌。ABPA的诊断较为困难。一个主要问题是在测定特异性IgE时缺乏标准化的过敏原,但有人提出使用重组过敏原以克服这一问题。本研究的目的是评估针对烟曲霉重组过敏原(rAsp)的IgE血清学检测是否有助于检测对该真菌的致敏情况以及ABPA的诊断。

方法

这是一项观察性横断面研究。在65名对烟曲霉有即刻皮肤反应性的哮喘患者中,依据经典标准进行ABPA的诊断。之后,测定针对rAsp f 1、rAsp f 2、rAsp f 3、rAsp f 4和rAsp f 6的IgE血清滴度。为比较确诊和排除ABPA诊断的患者之间的差异,采用双侧Fisher精确检验。

结果

尽管65名患者中有19名患者的IgE针对至少一种重组过敏原,但依据经典标准仅6名患者被诊断为该病。其中一名患者的IgE针对所有检测的重组过敏原,另一名患者有针对Asp f 3的抗体。

讨论

在该组患者中,测定针对重组烟曲霉过敏原的血清IgE对ABPA的诊断无助,对检测真菌致敏情况也无帮助。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验