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多克隆B细胞活化后肾小球中独特型-抗独特型免疫复合物的沉积。

Deposition of idiotype-anti-idiotype immune complexes in renal glomeruli after polyclonal B cell activation.

作者信息

Goldman M, Rose L M, Hochmann A, Lambert P H

出版信息

J Exp Med. 1982 May 1;155(5):1385-99. doi: 10.1084/jem.155.5.1385.

Abstract

We investigated the possible role of idiotypic interactions in the pathogenesis of the glomerular lesions observed in mice undergoing polyclonal B cell activation. BALB/c mice were studied for the presence of renal deposits of T15 idiotype-anti-T15 idiotype-immune complexes (IC) after injection of bacterial lipopolysaccharides (LPS). The T15 idiotype is the major idiotype of BALB/c mice anti-phosphorylcholine (PC) antibodies, which are cross-reactive with the idiotype of the TEPC-15 myeloma protein. This model was used because T15 idiotype-anti-T15 idiotype IC have been detected in the circulation of BALB/c mice after polyclonal B cell activation. First, an idiotype-specific immunofluorescence technique allowed us to detect T15 idiotype-bearing immunoglobulins in glomeruli from day 6 to day 28 after LPS injection. Second, fluorescein isothiocyanate-conjugated TEPC-15 myeloma protein was found to localize in the glomeruli after in vivo injection 18 d after LPS administration. This renal localization was shown to be idiotype-specific and could be quantified in a trace-labeling experiment. Third, kidney-deposited immunoglobulins of mice injected with LPS were eluted, radiolabeled, and analyzed by radioimmunoassay. Both T15 idiotype-bearing immunoglobulins and anti-T15 idiotype antibodies were detected in the eluates, providing further evidence for a renal deposition of T15 idiotype-anti-T15 idiotype IC. Polyclonal B cell activation is likely to result in a simultaneous triggering of many idiotypic clones and of corresponding anti-idiotypic clones represented in the B cell repertoire. This could lead to the formation of a variety of idiotype-anti-idiotype IC that could participate in the development of glomerular lesions.

摘要

我们研究了独特型相互作用在接受多克隆B细胞激活的小鼠所观察到的肾小球病变发病机制中的可能作用。在给BALB/c小鼠注射细菌脂多糖(LPS)后,研究其肾脏中T15独特型 - 抗T15独特型免疫复合物(IC)沉积情况。T15独特型是BALB/c小鼠抗磷酸胆碱(PC)抗体的主要独特型,该抗体与TEPC - 15骨髓瘤蛋白的独特型具有交叉反应性。使用此模型是因为在多克隆B细胞激活后,已在BALB/c小鼠的循环中检测到T15独特型 - 抗T15独特型IC。首先,一种独特型特异性免疫荧光技术使我们能够在LPS注射后第6天至第28天检测肾小球中携带T15独特型的免疫球蛋白。其次,发现异硫氰酸荧光素偶联的TEPC - 15骨髓瘤蛋白在LPS给药后18天体内注射后定位于肾小球。这种肾脏定位显示为独特型特异性,并且可以在微量标记实验中进行定量。第三,对注射LPS的小鼠肾脏沉积的免疫球蛋白进行洗脱、放射性标记并通过放射免疫测定法分析。在洗脱物中检测到携带T15独特型的免疫球蛋白和抗T15独特型抗体,为T15独特型 - 抗T15独特型IC的肾脏沉积提供了进一步证据。多克隆B细胞激活可能导致同时触发许多独特型克隆以及B细胞库中相应的抗独特型克隆。这可能导致形成各种独特型 - 抗独特型IC,它们可能参与肾小球病变的发展。

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Idiotypes and autoimmunity.独特型与自身免疫
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