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囊性纤维化患者和特发性支气管扩张患者血清及支气管肺泡灌洗液中的抗中性粒细胞胞浆抗体(ANCA)

Anti-neutrophil cytoplasmic antibodies (ANCA) in serum and bronchoalveolar lavage fluids of cystic fibrosis patients and patients with idiopathic bronchiectasis.

作者信息

Cobanoğlu Nazan, Ozcelik Uğur, Cetin Ilker, Yalçin Ebru, Doğru Deniz, Kiper Nural, Bakkaloğlu Ayşin

机构信息

Unit of Pediatric Pulmonary Diseases, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

出版信息

Turk J Pediatr. 2010 Jul-Aug;52(4):343-7.

PMID:21043377
Abstract

We investigated the presence of anti-neutrophil cytoplasmic antibodies (ANCA) in the serum and bronchoalveolar lavage fluid (BALF) of 21 cystic fibrosis (CF), 7 idiopathic bronchiectasis (IBR), and 11 control children and the relation between ANCA and any bacteria grown in BALF. Six of the CFs, but none of the IBRs or controls had positive serum cytoplasmic or perinuclear-ANCA (c-ANCA, p-ANCA). Serum autoantibodies against bactericidal/permeability increasing protein (BPI-ANCA) were positive in 2 CFs, 1 IBR and 1 control. While none of the CFs, IBRs or controls had positive BALF (c- or p-ANCA), 1 CF, 1 IBR and none of the controls had positive BALF BPI-ANCA. Pseudomonas aeruginosa was not grown in the specimens of any of the subjects. As the number of the patients in our study was very limited, further longitudinal and well-designed studies are necessary to show whether or not the presence of ANCA in serum or BALF relates to the presence of P. aeruginosa infection in the airways of CF and IBR patients.

摘要

我们调查了21例囊性纤维化(CF)、7例特发性支气管扩张(IBR)患儿以及11例对照儿童血清和支气管肺泡灌洗液(BALF)中抗中性粒细胞胞浆抗体(ANCA)的存在情况,以及ANCA与BALF中培养出的任何细菌之间的关系。6例CF患儿血清胞浆型或核周型ANCA(c-ANCA、p-ANCA)呈阳性,但IBR患儿和对照儿童均无阳性。2例CF患儿、1例IBR患儿和1例对照儿童血清中抗杀菌/通透性增加蛋白抗体(BPI-ANCA)呈阳性。虽然CF患儿、IBR患儿和对照儿童的BALF中(c-ANCA或p-ANCA)均无阳性,但1例CF患儿、1例IBR患儿的BALF中BPI-ANCA呈阳性,对照儿童均为阴性。所有受试者的标本中均未培养出铜绿假单胞菌。由于我们研究中的患者数量非常有限,因此有必要进行进一步的纵向和精心设计的研究,以确定血清或BALF中ANCA的存在是否与CF和IBR患者气道中铜绿假单胞菌感染的存在有关。

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Anti-neutrophil cytoplasmic antibodies (ANCA) in serum and bronchoalveolar lavage fluids of cystic fibrosis patients and patients with idiopathic bronchiectasis.囊性纤维化患者和特发性支气管扩张患者血清及支气管肺泡灌洗液中的抗中性粒细胞胞浆抗体(ANCA)
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Anti-neutrophil cytoplasmatic antibodies and lung disease in cystic fibrosis.囊性纤维化中的抗中性粒细胞胞浆抗体与肺部疾病
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Autoantibody response to BPI predict disease severity and outcome in cystic fibrosis.对杀菌/通透性增加蛋白(BPI)的自身抗体反应可预测囊性纤维化的疾病严重程度和预后。
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Pseudomonas aeruginosa in cystic fibrosis: pyocyanin negative strains are associated with BPI-ANCA and progressive lung disease.铜绿假单胞菌在囊性纤维化中的作用:绿脓菌素阴性菌株与 BPI-ANCA 及进行性肺病有关。
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Anti-neutrophil cytoplasmic antibodies directed against the bactericidal/permeability-increasing protein (BPI) in pediatric cystic fibrosis patients do not recognize N-terminal regions important for the anti-microbial and lipopolysaccharide-binding activity of BPI.针对小儿囊性纤维化患者中杀菌/通透性增加蛋白(BPI)的抗中性粒细胞胞浆抗体不能识别对BPI的抗菌和脂多糖结合活性很重要的N端区域。
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Extensive endoscopic image-guided sinus surgery decreases BPI-ANCA in patients with cystic fibrosis.广泛的内镜引导鼻窦手术可降低囊性纤维化患者的 BPI-ANCA。
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[Anti-Pseudomonas aeruginosa antibodies, circulating immune complexes, and anticytoplasm antibodies of neutrophils in patients with cystic fibrosis with and without Pseudomonas aeruginosa colonization].[患有和未患有铜绿假单胞菌定植的囊性纤维化患者体内的抗铜绿假单胞菌抗体、循环免疫复合物及中性粒细胞抗细胞质抗体]
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Antineutrophil cytoplasmic autoantibodies (ANCA) in children with cystic fibrosis.囊性纤维化患儿的抗中性粒细胞胞浆自身抗体(ANCA)
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引用本文的文献

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Prevalence of Bactericidal/Permeability-Increasing Protein Autoantibodies in Cystic Fibrosis Patients: Systematic Review and Meta-Analysis.囊性纤维化患者中杀菌/通透性增加蛋白自身抗体的患病率:系统评价和荟萃分析
Pediatr Allergy Immunol Pulmonol. 2019 Jun 1;32(2):45-51. doi: 10.1089/ped.2018.0970. Epub 2019 Jun 17.