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凝血因子 VIII 凝血抗原的简易免疫放射分析

Simplified immunoradiometric assay for factor VIII coagulant antigen.

作者信息

Thomas K B, Howard M A, Koutts J, Firkin B G

出版信息

Br J Haematol. 1982 May;51(1):47-57. doi: 10.1111/j.1365-2141.1982.tb07288.x.

Abstract

A simplified, non-competitive, solid phase immunoradiometric assay has been developed for the quantitation of factor VIII coagulant antigen (VIII:CAg)--the antigenic counterpart of FVIII coagulant activity (VIII:C). Both homologous and heterologous antibodies to human factor VIII (FVIII) were used in this assay. Initially, FVIII in a test sample was attached to immobilized, human IgG obtained from a polytransfused haemophilia A patient with a high titre antibody to VIII:C. The bound FVIII was then detected using rabbit 125I-IgG specific for human FVIII. The concentration of VIII:CAg correlated well with VIII:C levels in the plasma from normal donors (r = 0.84, n - 15). Homozygote von Willebrand's disease patients had undetectable levels of VIII:CAg in their plasma. Patients with severe haemophilia A (VIII:C less than 0.01 u/ml) could be divided into groups on the basis of the VIII:CAg levels, i.e. those having undetectable VIII:CAg and other with measurable VIII:CAg. VIII:CAg detected in normal serum was less than 0.002 u/ml. In this assay the use of human antibody to FVIII is considerably decreased compared to other methods for VIII:CAg, and the time-consuming steps to immunopurify human anti-FVIII antibody are eliminated.

摘要

已开发出一种简化的、非竞争性的固相免疫放射分析方法,用于定量因子VIII凝血抗原(VIII:CAg)——FVIII凝血活性(VIII:C)的抗原对应物。该分析方法使用了针对人因子VIII(FVIII)的同源和异源抗体。最初,将测试样品中的FVIII附着于从一名对VIII:C具有高滴度抗体的多次输血的甲型血友病患者获得的固定化人IgG上。然后使用对人FVIII特异的兔125I-IgG检测结合的FVIII。VIII:CAg的浓度与正常供体血浆中的VIII:C水平相关性良好(r = 0.84,n = 15)。纯合子血管性血友病患者血浆中VIII:CAg水平检测不到。重度甲型血友病患者(VIII:C低于0.01 u/ml)可根据VIII:CAg水平分为两组,即VIII:CAg检测不到的患者和VIII:CAg可测量的其他患者。正常血清中检测到的VIII:CAg低于0.002 u/ml。在该分析方法中,与其他VIII:CAg检测方法相比,人抗FVIII抗体的使用量大幅减少,并且省去了免疫纯化人抗FVIII抗体的耗时步骤。

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