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选择性IgA缺乏症患者体内的人抗IgM同种抗体。

Human anti-IgM iso-antibodies in subjects with selective IgA deficiency.

作者信息

Wells J V, Bleumers J F, Fudenberg H H

出版信息

Clin Exp Immunol. 1972 Nov;12(3):305-13.

Abstract

IgG-class iso-antibodies against human IgM (reverse rheumatoid factors') were detected in titres from 1:4 to 1:1024 in the serum of twelve of forty subjects (30%) with selective IgA deficiency. The antibodies were detected in a haemagglutination system with red cells coated by the chromic chloride method with proteins from a panel including nineteen Waldenström macroglobulins. The forty subjects included seventeen normal subjects, ten with recurrent infections, seven with ataxia telangiectasia, two each with asthma and lymphoma and one each with rheumatoid arthritis and chronic active hepatitis. Four of the twelve positive sera contained class-specific anti-IgM' which reacted with all or most of the IgM coats. The eight sera containing `anti-IgM of limited specificity' included six reacting with only one IgM coat, one reacting with two IgM coats and one reacting with four IgM coats. The anti-IgM in the latter serum defined an inherited allotypic marker on these four IgM proteins. There was no significant correlation between the presence of anti-IgM antibodies and the clinical status, sex and age of the patient nor the presence of antibodies against human IgG, human IgA and ruminant proteins. These antibodies against human IgM represent yet another immunologic abnormality in this group of patients.

摘要

在40名选择性IgA缺乏症患者中,有12名(30%)的血清中检测到了抗人IgM的IgG类同种抗体(“反向类风湿因子”),滴度从1:4到1:1024。这些抗体是在一个血凝系统中检测到的,该系统使用氯化铬法用包括19种瓦尔登斯特伦巨球蛋白在内的一组蛋白质包被红细胞。这40名受试者包括17名正常受试者、10名反复感染患者、7名共济失调毛细血管扩张症患者、2名哮喘患者、2名淋巴瘤患者、1名类风湿性关节炎患者和1名慢性活动性肝炎患者。12份阳性血清中有4份含有“类特异性抗IgM”,可与所有或大多数IgM包被发生反应。8份含有“特异性有限的抗IgM”的血清中,6份仅与一种IgM包被发生反应,1份与两种IgM包被发生反应,1份与四种IgM包被发生反应。后一份血清中的抗IgM定义了这四种IgM蛋白上的一种遗传同种异型标记。抗IgM抗体的存在与患者的临床状态、性别和年龄以及抗人IgG、抗人IgA和抗反刍动物蛋白抗体的存在之间没有显著相关性。这些抗人IgM抗体代表了这组患者中的又一种免疫异常。

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