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通过免疫印迹法和酶联免疫吸附测定法检测囊性纤维化合并变应性支气管肺曲霉病患者血清中的抗烟曲霉抗体

Serum anti-Aspergillus fumigatus antibodies by immunoblot and ELISA in cystic fibrosis with allergic bronchopulmonary aspergillosis.

作者信息

Knutsen A P, Mueller K R, Hutcheson P S, Slavin R G

机构信息

Pediatric Research Institute, St. Louis University Medical Center, MO 63104.

出版信息

J Allergy Clin Immunol. 1994 May;93(5):926-31. doi: 10.1016/0091-6749(94)90387-5.

DOI:10.1016/0091-6749(94)90387-5
PMID:8182235
Abstract

Allergic bronchopulmonary aspergillosis (ABPA) occurs with a prevalence of 5% to 15% in patients with cystic fibrosis (CF). Because of the frequent colonization with Aspergillus fumigatus (Af) in CF, the causative agent of ABPA, antibody reactivity to Af proteins is frequently observed, which obscures the diagnosis of ABPA. Patients with CF are also categorized according to the presence of positive skin test responses to Af and/or the presence of positive precipitins. In this study we used ELISA and immunoblot assay to detect IgE and IgG anti-Af antibodies in patients with CF and ABPA (n = 13) compared with other groups of patients with CF: those with positive skin test and positive precipitin results (n = 18), those with positive skin test and negative precipitin results (n = 14), those with negative skin test and positive precipitin results (n = 10), and those with negative skin test and negative precipitin results (n = 35). IgE and IgG anti-Af antibodies were significantly elevated in patients with ABPA as determined by both immunoblot assay (p < 0.01) and ELISA (p < 0.01). However, detection of Af antibodies by ELISA was more sensitive in discriminating patients with CF and ABPA from patients with CF who had positive skin test and positive precipitin results but lacked radiographic and clinical evidence of ABPA. In patients with CF and ABPA the immunoblot assays demonstrated a multitude of IgE, IgG, and IgA antibody responses to Af proteins, which ranged in molecular weight from 14 kd to greater than 106 kd. The level of IgE anti-Af antibody to individual proteins decreased during remissions of ABPA.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

变应性支气管肺曲霉病(ABPA)在囊性纤维化(CF)患者中的患病率为5%至15%。由于CF患者常被烟曲霉(Af)定植,而Af是ABPA的病原体,因此常观察到对Af蛋白的抗体反应性,这使得ABPA的诊断变得模糊。CF患者也根据对Af皮肤试验反应阳性和/或沉淀素阳性进行分类。在本研究中,我们使用酶联免疫吸附测定(ELISA)和免疫印迹分析来检测CF合并ABPA患者(n = 13)与其他CF患者组中抗Af的IgE和IgG抗体:皮肤试验阳性且沉淀素结果阳性的患者(n = 18)、皮肤试验阳性且沉淀素结果阴性的患者(n = 14)、皮肤试验阴性且沉淀素结果阳性的患者(n = 10)以及皮肤试验阴性且沉淀素结果阴性的患者(n = 35)。通过免疫印迹分析(p < 0.01)和ELISA(p < 0.01)确定,ABPA患者中抗Af的IgE和IgG抗体显著升高。然而,在区分CF合并ABPA患者与皮肤试验阳性且沉淀素结果阳性但缺乏ABPA影像学和临床证据的CF患者时,ELISA检测Af抗体更为敏感。在CF合并ABPA患者中,免疫印迹分析显示对Af蛋白有多种IgE、IgG和IgA抗体反应,分子量范围从14 kd到大于106 kd。在ABPA缓解期,针对单个蛋白的抗Af IgE抗体水平下降。(摘要截短至250字)

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