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促红细胞生成素的放射免疫测定:正常人类受试者和造血系统疾病患者的血清水平

A radioimmunoassay for erythropoietin: serum levels in normal human subjects and patients with hemopoietic disorders.

作者信息

Rege A B, Brookins J, Fisher J W

出版信息

J Lab Clin Med. 1982 Dec;100(6):829-43.

PMID:7142788
Abstract

An RIA for Ep has been developed that is highly sensitive and specific. A homogeneous Ep preparation was labeled with 125 I by the chloramine-T method to a specific activity of 90 to 136 micro Ci/microgram and immunoreactivity of 80%. Ep antiserum, which was produced to a human urinary Ep preparation (80 U/mg of protein), was adsorbed with normal human urinary and serum proteins without any loss in sensitivity of the RIA to increase the specificity of the assay. A good correlation was seen between the RIA and the exhypoxic polycythemic mouse assay (corr. coef. 0.967; slope 1.05 and "y" intercept 0.75). Ep titers in sera from 175 hematologically normal human subjects exhibited a normal frequency distribution and ranged between 5.8 and 36.6 mU/ml with a mean of 14.9 +/- 4.7 (S.D.) and median of 14.3 Serum Ep titers were markedly elevated in seven patients with aplastic anemia and one patient with pure red cell aplasia (1350 to 20,640 mU/ml) and were lower than normal in two patients with polycythemia vera (8.1 and 9.4 mU/ml). The serum Ep titers in a prenephrectomy patient with chronic glomerulonephritis (32.1 mU/ml) decreased to below normal levels (9.04 mU/ml) after nephrectomy. The cord serum erythropoietin titers in 10 IDM [90.82 +/- 134.1 (S.D.) mu/ml] returned to values within the normal range (13.86 +/- 5.55) on day 3 after birth, suggesting the utility of the RIA in elucidating the role of hypoxia and/or insulin in increased erythropoiesis in IDM. The serum Ep titers in patients with anemias and polycythemias were compared to those of normal human subjects and agreed well with pathophysiologic mechanisms of these hemopoietic disorders, confirming the validity of the RIA.

摘要

已开发出一种用于促红细胞生成素(Ep)的放射免疫分析方法,该方法具有高度的敏感性和特异性。用氯胺-T法将一种纯促红细胞生成素制剂用125I标记,比活度为90至136微居里/微克,免疫反应性为80%。针对人尿促红细胞生成素制剂(80单位/毫克蛋白质)产生的促红细胞生成素抗血清,用正常人尿和血清蛋白进行吸附,放射免疫分析的敏感性无任何损失,以提高检测的特异性。放射免疫分析与低氧性红细胞增多症小鼠试验之间存在良好的相关性(相关系数0.967;斜率1.05,“y”截距0.75)。175名血液学正常的人类受试者血清中的促红细胞生成素滴度呈现正态频率分布,范围在5.8至36.6毫微单位/毫升之间,平均值为14.9±4.7(标准差),中位数为14.3。7例再生障碍性贫血患者和1例纯红细胞再生障碍患者的血清促红细胞生成素滴度显著升高(1350至20640毫微单位/毫升),2例真性红细胞增多症患者的血清促红细胞生成素滴度低于正常水平(8.1和9.4毫微单位/毫升)。一名慢性肾小球肾炎患者在肾切除术前的血清促红细胞生成素滴度为(32.1毫微单位/毫升),肾切除术后降至正常水平以下(9.04毫微单位/毫升)。10名糖尿病母亲婴儿(IDM)的脐血促红细胞生成素滴度为[90.82±134.1(标准差)微单位/毫升],出生后第3天恢复到正常范围内的值(13.86±5.55),这表明放射免疫分析在阐明低氧和/或胰岛素在糖尿病母亲婴儿红细胞生成增加中的作用方面具有实用性。将贫血和红细胞增多症患者的血清促红细胞生成素滴度与正常人类受试者的进行比较,结果与这些造血疾病的病理生理机制相符,证实了放射免疫分析的有效性。

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