子痫前期血小板产生的免疫复合物和血管活性。

R L Medcalf, R J Kuhn, J D Mathews, R F Moulds
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引用次数: 4

摘要

体内血小板活化循环免疫复合物已被认为是潜在的机制之一,在先兆子痫。使用聚乙二醇蛋白- a免疫复合物测定法的改进,在20名诊断为子痫前期的患者中,有14名患者的免疫复合物超过相当于20微克/毫升的热聚集IgG。在19个正常对照中,只有6个被发现有相似水平的免疫复合物。此外,使用小体积生物测定法,发现热聚集IgG浓度超过20微克/毫升时,可以激活血小板,释放足够浓度的血管活性药物,从而在体外收缩人血管。这些结果支持了一种假设,即免疫复合物在体内激活血小板可以释放足够浓度的血管活性药物,从而导致子痫前期高血压的特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immune complexes and vasoactivity generated from platelets in pre-eclampsia.

In vivo platelet activation by circulating immune complexes has been suggested as one of the underlying mechanisms in preeclampsia. Using a modification of the polyethylene glycol protein-A immune complex assay, immune complexes were found in excess of the equivalent of 20 micrograms/ml heat aggregated IgG in fourteen out of twenty patients diagnosed as having pre-eclampsia. Only six out of nineteen normal controls were found to have similar levels of immune complexes. Furthermore, using a small volume bio-assay method, concentrations of heat aggregated IgG in excess of 20 micrograms/ml were found to activate platelets to release sufficient concentrations of vasoactive agents to constrict a human blood vessel in vitro. These results support the hypothesis that in vivo platelet activation by immune complexes can release sufficient concentrations of vasoactive agents to contribute to the hypertension characteristic of pre-eclampsia.

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