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[阻塞性肺疾病中的抗体缺乏]

[Antibody deficiency in obstructive lung diseases].

作者信息

Eibl M M, Pum M, Bernatowska E, Leibl H

机构信息

Institut für Immunologie, Universität Wien.

出版信息

Padiatr Padol. 1990;25(4):231-8.

PMID:2234987
Abstract

Severe chronic chest disease is the most serious complication in patients with antibody deficiency syndromes. IgG-subclass-deficiencies were a frequent finding in patients with obstructive lung disease and in patients with sinopulmonary infections. In the patient population referred to us for immunological investigation recurrent infection of the upper and lower respiratory tract was the most common reason to suspect undue susceptibility to infection. In 1034 pediatric patients analyzed 299 were found to be deficient in one of several IgG subclasses. In a group of 30 children, all of whom had severe lung disease and normal concentrations of serum IgG, IgA and IgM, airway-obstruction has been diagnosed in 19. 20 of the 30 patients had IgG-subclass-deficiency. The large percentage of IgG-subclass-deficiencies in this group of patients indicates that immunological disregulation is likely to contribute to the pathogenesis of chronic lung disease.

摘要

严重慢性胸部疾病是抗体缺乏综合征患者最严重的并发症。IgG亚类缺陷在阻塞性肺病患者和鼻窦肺部感染患者中很常见。在转诊至我们这里进行免疫学检查的患者群体中,上、下呼吸道反复感染是怀疑存在易感染倾向的最常见原因。在分析的1034例儿科患者中,发现299例存在几种IgG亚类之一的缺陷。在一组30名儿童中,所有儿童均患有严重肺部疾病且血清IgG、IgA和IgM浓度正常,其中19例被诊断为气道阻塞。30例患者中有20例存在IgG亚类缺陷。该组患者中IgG亚类缺陷的比例很高,表明免疫调节紊乱可能在慢性肺病的发病机制中起作用。

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