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IgA 肾病患者外周血淋巴细胞交叉反应性独特型抗体的表达与合成及其抗独特型抗体的抑制作用

Expression and synthesis of cross-reactive idiotypic antibodies by peripheral blood lymphocytes and their suppression by anti-idiotypes in patients with IgA nephropathy.

作者信息

González-Cabrero J, de Nicolas R, Hernando L, Egido J

机构信息

Fundación Jiménez Díaz, Autonoma University, Madrid, Spain.

出版信息

J Immunol. 1991 Dec 15;147(12):4162-6.

PMID:1753092
Abstract

We have recently described that patients with IgA nephropathy present high serum levels of anti-BSA idiotypic antibodies that were well correlated with the existence of hematuria. Furthermore, these Id were found in circulating and renal deposited immune complexes. In the present work, we examined the expression of surface idiotypic determinants on PBL by flow cytometry and their in vitro production, using as reagent anti-idiotypic antibodies previously well characterized. The presence of cross-reactive Id-bearing cells was observed in 5 out of 6 patients studied, with frequencies ranging from 3 to 12% of lymphocytes. After 7 days of culture, the spontaneous synthesis of idiotypic antibodies by PBL was found elevated in 6 out of 13 (46%) patients. A major Id cell expression and production was noted in patients with active disease as defined by hematuria. The preincubation of PBL with 20 and 50 micrograms of anti-idiotypic antibodies/2 x 10(6) cells for 3 days induced a significant inhibition of cross-reactive Id production in a dose-dependent fashion, with a degree of suppression between 12 and 50% in five out of six patients studied. In the above assays, as negative controls, we used the anti-Id antibodies previously adsorbed on an Id-Sepharose column. On the whole, these results suggest that patients with IgA nephropathy present dysfunctions in the Id-Anti-Id network that could play an important role in the pathogenesis of this disease.

摘要

我们最近描述了IgA肾病患者血清中抗牛血清白蛋白独特型抗体水平较高,且与血尿的存在密切相关。此外,这些独特型抗体存在于循环和肾脏沉积的免疫复合物中。在本研究中,我们使用先前已充分表征的抗独特型抗体作为试剂,通过流式细胞术检测外周血淋巴细胞(PBL)表面独特型决定簇的表达及其体外产生情况。在所研究的6例患者中,有5例观察到存在交叉反应性携带独特型抗体的细胞,其频率占淋巴细胞的3%至12%。培养7天后,发现13例患者中有6例(46%)的PBL自发合成独特型抗体增加。血尿定义的活动性疾病患者中观察到主要的独特型细胞表达和产生。用20和50微克抗独特型抗体/2×10⁶个细胞对PBL进行预孵育3天,以剂量依赖方式显著抑制交叉反应性独特型抗体的产生,在所研究的6例患者中有5例抑制程度在12%至50%之间。在上述试验中,作为阴性对照,我们使用先前吸附在独特型琼脂糖柱上的抗独特型抗体。总体而言,这些结果表明IgA肾病患者的独特型-抗独特型网络存在功能障碍,这可能在该疾病的发病机制中起重要作用。

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