首页> 外文期刊>The Journal of Experomental Medicine >Deposition of idiotype-anti-idiotype immune complexes in renal glomeruli after polyclonal B cell activation.
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Deposition of idiotype-anti-idiotype immune complexes in renal glomeruli after polyclonal B cell activation.

机译:多克隆B细胞激活后肾小球中独特型-抗独特型免疫复合物的沉积。

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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.
机译:我们调查了在经历多克隆B细胞活化的小鼠中观察到的肾小球病变的发病机制中独特型相互作用的可能作用。研究BALB / c小鼠在注射细菌性脂多糖(LPS)后是否存在T15型-抗-T15型-免疫复合物(IC)的肾脏沉积物。 T15独特型是BALB / c小鼠抗磷酸胆碱(PC)抗体的主要独特型,它与TEPC-15骨髓瘤蛋白的独特型具有交叉反应性。之所以使用该模型,是因为在多克隆B细胞激活后,在BALB / c小鼠的循环中已检测到T15独特型-抗T15独特型IC。首先,独特型免疫荧光技术使我们能够在LPS注射后第6天到第28天检测肾小球中T15型携带免疫球蛋白。其次,发现在LPS施用18天后体内注射后,荧光素异硫氰酸酯缀合的TEPC-15骨髓瘤蛋白位于肾小球。肾脏定位显示为独特型,可以在痕量标记实验中进行量化。第三,洗脱LPS的小鼠的肾脏沉积的免疫球蛋白被洗脱,放射性标记并通过放射免疫测定法进行分析。在洗脱液中同时检测到带有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的证据。多克隆B细胞激活可能会导致同时触发许多B型库中代表的独特型克隆和相应的抗独特型克隆。这可能导致形成各种可能参与肾小球病变发展的独特型-抗独特型IC。

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