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通过酶联免疫吸附测定法对慢性铜绿假单胞菌感染患者血清中抗铜绿假单胞菌的IgG亚类抗体进行研究。

IgG subclass antibodies to Pseudomonas aeruginosa in sera from patients with chronic Ps. aeruginosa infection investigated by ELISA.

作者信息

Pressler T, Pedersen S S, Espersen F, Høiby N, Koch C

机构信息

Department of Clinical Microbiology, Rigshospitalet, Copenhagen, Denmark.

出版信息

Clin Exp Immunol. 1990 Sep;81(3):428-34. doi: 10.1111/j.1365-2249.1990.tb05351.x.

Abstract

ELISAs using subclass-specific monoclonal antibodies were developed for the quantification of human IgG1, IgG2, IgG3 and IgG4 antibodies to Ps. aeruginosa. We investigated the pattern of IgG subclass antibodies against Ps. aeruginosa in serum from patients with cystic fibrosis (CF), other patients with chronic Ps. aeruginosa infection, and healthy controls. Healthy controls and patients with CF but without Ps. aeruginosa infection showed no or very low titres of antibodies against Ps. aeruginosa. In the early stage of chronic Ps. aeruginosa infection, antibody titres in all four subclasses were significantly higher than either normals or CF patients without infection. Other patients with Ps. aeruginosa infection showed the same increased level of IgG subclass antibodies as CF patients in an early stage of infection. Sixteen patients (eight in good and eight in poor clinical condition) have been followed for an average of 13 years with multiple serum samples covering the pre-infection, early and late stages of chronic infection. Patients in a poor clinical condition showed significantly higher levels of IgG3 antibodies in the first year of infection and 2 years later also had significantly higher IgG2 antibody levels. We conclude that elevated levels of IgG2 and IgG3 antibodies to Ps. aeruginosa are a sign of poor prognosis in CF.

摘要

利用亚类特异性单克隆抗体开发了酶联免疫吸附测定法(ELISA),用于定量检测人抗铜绿假单胞菌的IgG1、IgG2、IgG3和IgG4抗体。我们研究了囊性纤维化(CF)患者、其他慢性铜绿假单胞菌感染患者以及健康对照血清中抗铜绿假单胞菌的IgG亚类抗体模式。健康对照以及无铜绿假单胞菌感染的CF患者显示出无或极低滴度的抗铜绿假单胞菌抗体。在慢性铜绿假单胞菌感染的早期,所有四个亚类的抗体滴度均显著高于正常人和无感染的CF患者。其他铜绿假单胞菌感染患者在感染早期显示出与CF患者相同的IgG亚类抗体水平升高。16名患者(8名临床状况良好,8名临床状况不佳)被随访了平均13年,采集了多个血清样本,涵盖了慢性感染的感染前、早期和晚期阶段。临床状况不佳的患者在感染的第一年显示出显著更高的IgG3抗体水平,2年后IgG2抗体水平也显著更高。我们得出结论,CF患者中抗铜绿假单胞菌的IgG2和IgG3抗体水平升高是预后不良的一个迹象。

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