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肝素对阵发性夜间血红蛋白尿(PNH)红细胞补体激活及溶解的影响。

Effect of heparin on complement activation and lysis of paroxysmal nocturnal hemoglobinuria (PNH) red cells.

作者信息

Logue G L

出版信息

Blood. 1977 Aug;50(2):239-47.

PMID:17439
Abstract

The effect of heparin upon the binding of the third component of complement (C3) to PNH red cells in vitro and their subsequent hemolysis is described. Heparin, in increasing concentrations, progressively inhibits membrane C3 fixation and hemolysis when the classic complement pathway is activated by anti-red cell antibodies. Heparin has a biphasic effect upon membrane C3 fixation and hemolysis when complement is activated in serum at decreased ionic strength (sucrose lysis) or in serum at decreased pH (Ham test). Heparin in concentrations above 2 U/ml inhibits C3 binding and hemolysis while lower concentrations of heparin enhance the consequences of complement activation by these two procedures. This enhanced complement activation may explain the increased hemolysis sometimes reported in PNH patients treated with heparin, and suggests that heparin may aggravate the consequences of pathologic alternative pathway complement activation in other diseases.

摘要

本文描述了肝素对体外补体第三成分(C3)与阵发性睡眠性血红蛋白尿症(PNH)红细胞结合及其随后溶血的影响。当经典补体途径由抗红细胞抗体激活时,随着肝素浓度的增加,其逐渐抑制膜C3固定和溶血。当在离子强度降低的血清中(蔗糖溶血)或pH降低的血清中(汉姆试验)激活补体时,肝素对膜C3固定和溶血具有双相作用。浓度高于2 U/ml的肝素抑制C3结合和溶血,而较低浓度的肝素增强这两种方法激活补体的后果。这种增强的补体激活可能解释了有时报道的接受肝素治疗的PNH患者溶血增加的现象,并提示肝素可能会加重其他疾病中病理性替代途径补体激活的后果。

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