Furlong R A, Chesham J, Peake I R
Department of Haematology, University of Wales College of Medicine, Heath Park, Cardiff.
Clin Lab Haematol. 1988;10(3):295-305. doi: 10.1111/j.1365-2257.1988.tb00023.x.
Enzyme-linked immunosorbent assays (ELISA) for factor VIII antigen (VIII:Ag) and von Willebrand factor antigen (vWF:Ag) have been developed, each employing monoclonal antibodies. In the majority of severe haemophilic plasmas tested, VIII:Ag was undetectable by ELISA and also by immunoradiometric assay (IRMA) using haemophilic VIII:C antibodies. In haemophilic plasmas with mild/moderate deficiency of coagulant factor VIII (VIII:C), there was no significant difference between the two immunoassays although there was a general trend for ELISA VIII:Ag results to be higher. Assay of von Willebrand's disease (vWd) plasmas with the ELISA for vWF:Ag demonstrated reduced levels of this antigen in type I vWd, normal levels in type IIA, and a severe reduction of vWF:Ag in type III vWd. The discrimination of obligate carriers of haemophilia from normal was determined using ratios of factor VIII/vWF. Factor VIII antigen/von Willebrand factor antigen measured by IRMA and Laurell immunoelectrophoresis respectively, gave a superior discriminant to that of VIII:C/vWF:Ag (Laurell), but optimal discrimination was obtained with the combination of ELISAs for VIII:Ag and vWF:Ag.
已经开发出用于检测因子VIII抗原(VIII:Ag)和血管性血友病因子抗原(vWF:Ag)的酶联免疫吸附测定(ELISA),每种方法都使用单克隆抗体。在大多数检测的重度血友病血浆中,ELISA检测不到VIII:Ag,使用血友病VIII:C抗体的免疫放射测定(IRMA)也检测不到。在凝血因子VIII(VIII:C)轻度/中度缺乏的血友病血浆中,两种免疫测定之间没有显著差异,尽管ELISA VIII:Ag结果总体上有更高的趋势。用ELISA检测血管性血友病(vWd)血浆中的vWF:Ag,结果显示I型vWd中该抗原水平降低,IIA型中水平正常,III型vWd中vWF:Ag严重降低。利用因子VIII/vWF的比值来区分血友病的 obligate携带者和正常人。分别通过IRMA和劳雷尔免疫电泳测量的因子VIII抗原/血管性血友病因子抗原,比VIII:C/vWF:Ag(劳雷尔法)具有更好的区分能力,但使用ELISA检测VIII:Ag和vWF:Ag的组合可获得最佳区分效果。