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IgA 肾小球肾炎(伯杰氏病):血清中高聚合 IgA 水平的证据。

IgA glomerulonephritis (Berger's disease): evidence of high serum levels of polymeric IgA.

作者信息

Trascasa M L, Egido J, Sancho J, Hernando L

出版信息

Clin Exp Immunol. 1980 Nov;42(2):247-54.

Abstract

Eleven out of 15 patients with IgA mesangial glomerulonephritis (Berger's disease) had an increased proportion of serum IgA in 9-21S fractions on 5-40% sucrose density-gradient ultracentrifugation; the heavier fractions decreased at acid pH. Serum IgA purified by starch electrophoresis was subjected to reduction-alkylation yielding fragments of lower molecular weight. J chain was detected on urea alkaline polyacrylamide electrophoresis and the high-molecular weight IgA bound the human secretory component. In six patients treated with phenytoin for 1 year there was a decrease in polymeric IgA and an increase in monomeric IgA adopting a pattern similar to that of the controls. Our results show the presence of a large amount of true IgA polymers, partially as immune complexes, in the serum of patients with Berger's disease. These data together with their normalization after phenytoin treatment may open a new pathogenic and therapeutic approach to this entity.

摘要

15例IgA系膜增生性肾小球肾炎(伯杰氏病)患者中,11例在5%-40%蔗糖密度梯度超速离心时,9-21S组分的血清IgA比例增加;在酸性pH条件下,较重的组分减少。经淀粉电泳纯化的血清IgA进行还原烷基化反应,产生较低分子量的片段。在尿素碱性聚丙烯酰胺电泳上检测到J链,高分子量IgA与人分泌成分结合。6例接受苯妥英治疗1年的患者,聚合IgA减少,单体IgA增加,其模式与对照组相似。我们的结果表明,伯杰氏病患者血清中存在大量真正的IgA聚合物,部分以免疫复合物形式存在。这些数据以及苯妥英治疗后它们的正常化,可能为该疾病开辟新的致病机制和治疗途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8433/1537109/cd657b8dfcbb/clinexpimmunol00188-0051-a.jpg

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