囊性纤维化中的铜绿假单胞菌感染。铜绿假单胞菌黏液菌株与体液免疫反应的关系。

N. Høiby
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引用次数: 120

摘要

本文对70例囊性纤维化患者呼吸道中铜绿假单胞菌的发生情况和患者血清中铜绿假单胞菌沉淀的发生情况进行了调查,方法是每月对患者的气管分泌物进行细菌学检查,并对患者血清中铜绿假单胞菌的多价抗原进行交叉免疫电泳。铜绿假单胞菌的1年患病率为64%。在新定植的患者和间歇性定植的患者中,非粘液样菌株占主导地位,而在长期定植的患者中,粘液样菌株占主导地位。黏液样菌株的发生,特别是在慢性定植的患者中,与非黏液样菌株的发生相比,与铜绿假单胞菌的沉淀数量显著增加有关。黏液样菌长期定殖的雄虫沉淀蛋白的数量明显高于雌性,且沉淀蛋白的数量与铜绿假单胞菌长期定殖的时间有关。结果与粘液样物质可能是一种毒力因子的假设一致,因为它可能抑制沉淀素对粘液样细胞的调节作用和细胞的补体依赖性裂解,从而在囊性纤维化患者的呼吸道中有利于粘液样菌株而牺牲非粘液样菌株。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pseudomonas aeruginosa infection in cystic fibrosis. Relationship between mucoid strains of Pseudomonas aeruginosa and the humoral immune response.
The occurrence of Pseudomonas aeruginosa in the respiratory tract of 70 cystic fibrosis patients and the occurrence of precipitins against Ps. aeruginosa in sera from the same patients have been investigated during one year by means of monthly bacteriological examinations of tracheal secretions and by means of crossed Immunoelectrophoresis of a polyvalent Ps. aeruginosa antigen against sera from the patients. The one-year period prevalence rate of patients harbouring Ps. aeruginosa was 64 per cent. In newly colonized patients and in intermittently colonized patients non-mucoid strains were predominating, whereas mucoid strains were predominating in chronically colonized patients. The occurrence of mucoid strains, especially in chronically colonized patients, was associated with a significantly higher number of precipitins against Ps. aeruginosa than the occurrence of non-mucoid strains. Males chronically colonized with mucoid strains presented a significantly higher number of precipitins than females chronically colonized with mucoid strains and the number of precipitins was correlated with the duration of the chronic colonization with Ps. aeruginosa in males in contrast to females. The results are in accordance with the hypothesis that mucoid substance could be a virulence factor because it might inhibit the opsonizing effect of the precipitins on the mucoid cells and the complement dependent lysis of the cells hereby favouring mucoid strains at the expense of non-mucoid strains in the respiratory tract of cystic fibrosis patients.
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