Green D, Reynolds N
Clin Chem. 1977 Sep;23(9):1648-53.
A plasma protein required for the support of ristocetin-induced platelet aggregation was isolated from antihemophilic factor concentrate and radiolabeled with 125I. A double-antibody radioimmunoassay was developed, with use of specific rabbit anti-VIII related antigen serum and goat anti-rabbit globulin. The assay is sensitive, reproducible, and technically simple to perform. Values obtained in normal subjects ranged from 0.65 to 1.53 units, similar to our normal range for VIII coagulant activity (0.67-1.43 units). However, normal or increased values of VIII-related antigen were observed in VIII coagulant-deficient hemophiliacs. Also, concentrations of VII-related antigen significantly exceeded coagulant concentrations in several patients with liver disease or disseminated intravascular coagulation, or both. Of a broad selection of congenital coagulation disorders examined, only patients with von Willebrand's disease had decreased VIII-related antigen concentrations, and these corresponded to the lowered concentration of ristocetin cofactor in the patients. In three transfused patients, VII-related antigen values correlated with the concentration of the cofactor. Our results suggest that the radioimmunoassay of VIII-related antigen is a simple and valuable adjunct in the study of patients with clotting abnormalities.
从抗血友病因子浓缩物中分离出一种支持瑞斯托霉素诱导的血小板聚集所需的血浆蛋白,并用125I进行放射性标记。利用特异性兔抗VIII相关抗原血清和山羊抗兔球蛋白建立了双抗体放射免疫测定法。该测定法灵敏、可重复且技术操作简单。正常受试者的测定值范围为0.65至1.53单位,与我们VIII凝血活性的正常范围(0.67 - 1.43单位)相似。然而,在VIII凝血因子缺乏的血友病患者中观察到VIII相关抗原值正常或升高。此外,在一些患有肝病或弥散性血管内凝血或两者皆有的患者中,VII相关抗原的浓度显著超过凝血因子浓度。在所检查的多种先天性凝血障碍中,只有血管性血友病患者的VIII相关抗原浓度降低,且这些浓度与患者体内瑞斯托霉素辅因子浓度降低相对应。在三名输血患者中,VII相关抗原值与辅因子浓度相关。我们的结果表明,VIII相关抗原的放射免疫测定在凝血异常患者的研究中是一种简单且有价值的辅助手段。