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肾病综合征患儿尿液和血浆中哈格曼因子的免疫定量分析。

Immunoquantitation of Hageman factor in urine and plasma of children with nephrotic syndrome.

作者信息

Hruby M A, Honig G R, Shapira E

出版信息

J Lab Clin Med. 1980 Sep;96(3):501-10.

PMID:6772722
Abstract

Children with nephrotic syndrome frequently have decreased plasma levels of Hageman factor (factor XII). Studies were designed to determine whether this finding results primarily from a loss of Hageman factor in the urine or is related to an alteration in the Hageman factor protein itself. A monospecific anti-Hageman factor goat antibody was prepared and used for quantitative measurements of Hageman factor in urine and plasma by a radial immunodiffusion method. Samples of 24 hr urine collections from 14 children with nephrotic syndrome were examined by this immunoassay technique; no Hageman factor was detected in the urine in 13/14 patients. Comparative studies using plasma from the nephrotic syndrome patients and nine normal controls demonstrated: (1) a significantly reduced level of Hageman ACT in the nephrotic syndrome patients (p < 0.001); (2) a reduction to a lesser degree of the levels of CRM in the same group (p < 0.001); and (3) a significantly increased CRM/ACT ratio in the plasma of the patients with nephrotic syndrome (p < 0.01) indicating partial inactivation of the Hageman factor enzymatic function. However, no inhibitory activity to added Hageman factor could be detected in the plasma or urine of the patients. These findings indicate that the decreased plasma Hageman factor activity that accompanies the nephrotic syndrome cannot be adequately explained by simple urinary loss of Hageman factor as has previously been suggested.

摘要

患有肾病综合征的儿童血浆中Hageman因子(因子XII)水平常常降低。开展了多项研究以确定这一发现主要是由于尿液中Hageman因子的丢失,还是与Hageman因子蛋白本身的改变有关。制备了一种单特异性抗Hageman因子山羊抗体,并通过放射免疫扩散法用于定量测定尿液和血浆中的Hageman因子。采用这种免疫测定技术对14例肾病综合征患儿的24小时尿液样本进行了检测;14例患者中有13例尿液中未检测到Hageman因子。对肾病综合征患者的血浆与9名正常对照者进行的对比研究表明:(1)肾病综合征患者的Hageman促凝活性水平显著降低(p<0.001);(2)同一组中交叉反应物质(CRM)水平有较小程度的降低(p<0.001);(3)肾病综合征患者血浆中的CRM/促凝活性比值显著升高(p<0.01),表明Hageman因子的酶功能部分失活。然而,在患者的血浆或尿液中未检测到对添加的Hageman因子的抑制活性。这些发现表明,如先前所认为的,肾病综合征伴有的血浆Hageman因子活性降低不能通过简单的Hageman因子经尿液丢失来充分解释。

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