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特发性IgA系膜肾病(伯杰氏病)中的聚合性IgA类风湿因子

Polymeric IgA rheumatoid factor in idiopathic IgA mesangial nephropathy (Berger's disease).

作者信息

Sinico R A, Fornasieri A, Oreni N, Benuzzi S, D'Amico G

出版信息

J Immunol. 1986 Jul 15;137(2):536-41.

PMID:3722816
Abstract

A specific and sensitive enzyme-linked immunosorbent assay (ELISA) was used to detect IgA rheumatoid factor (RF) in sera from 88 patients with IgA nephropathy (IgA GN), a disease characterized by abnormalities of IgA production. Significantly higher levels of IgA antiglobulins were demonstrated in IgA GN patients than in normal healthy controls and patients with other forms of chronic primary glomerulonephritis (mean +/- SEM 28.4 +/- 6.6 vs 6.0 +/- 0.4 and 8.3 +/- 1.2 micrograms/ml respectively; p less than 0.002). Interestingly, in contrast to rheumatoid arthritis, IgA RF activity was not associated with IgM antiglobulins. Analysis of sera fractionated by gel chromatography at acid pH revealed that anti-IgG activity resided predominantly in the polymeric fractions of IgA as confirmed by the ability to bind "free" secretory component. Several findings in patients with IgA GN suggest that the IgA deposited in the glomeruli is polymeric, and levels of circulating macromolecular IgA are increased. Our findings confirm a general perturbation of IgA metabolism in this disease. Although the polymeric nature of the IgA RF is suggestive of a mucosal origin, additional evidence is needed to confirm this hypothesis.

摘要

采用一种特异性和敏感性均较高的酶联免疫吸附测定法(ELISA),检测88例IgA肾病(IgA GN)患者血清中的IgA类风湿因子(RF)。IgA肾病是一种以IgA产生异常为特征的疾病。结果显示,IgA GN患者血清中IgA抗球蛋白水平显著高于正常健康对照者及其他形式的慢性原发性肾小球肾炎患者(分别为平均±标准误28.4±6.6 vs 6.0±0.4和8.3±1.2微克/毫升;p<0.002)。有趣的是,与类风湿关节炎不同,IgA RF活性与IgM抗球蛋白无关。对酸性pH条件下经凝胶色谱分离的血清分析显示,抗IgG活性主要存在于IgA的多聚体部分,这一点通过结合“游离”分泌成分的能力得到证实。IgA GN患者的多项研究结果表明,沉积于肾小球的IgA是多聚体,且循环中大分子IgA水平升高。我们的研究结果证实了该疾病中IgA代谢的普遍紊乱。尽管IgA RF的多聚体性质提示其起源于黏膜,但还需要更多证据来证实这一假说。

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