Holmberg L, Borge L, Ljung R, Nilsson I M
Scand J Haematol. 1979 Jul;23(1):17-24. doi: 10.1111/j.1600-0609.1979.tb02847.x.
Antihaemophilic-factor-A-antibodies, which had spontaneously arisen in 2 patients, were used to develop an immunoradiometric method for measurement of antihaemophilic factor A antigen (VIII:CAg). 13 patients with severe haemophilia A had VII:CAg below the limit of detection (0.01 U/ml). Patients with moderate and mild haemophilia A either had VII:CAg roughly equal to factor VIII clotting activity (VIII:C) or a not detectable VII:CAg, suggesting 2 different molecular mechanisms in moderate and mild haemophilia A. VIII:CAg could be detected in serum but in lower amounts than in plasma. In 2 patients with von Willebrand's disease VIII:CAg equalled VII:C. The post-transfusional retarded increase of VII:C in 1 patient with von Willebrand's disease was accompanied by a slight increase in VIII:CAg. Fetal plasma contained measurable amounts of VII:CAg.
在2名患者中自发产生的抗血友病因子A抗体被用于开发一种免疫放射分析法,以测定抗血友病因子A抗原(VIII:CAg)。13名重度甲型血友病患者的VII:CAg低于检测限(0.01 U/ml)。中度和轻度甲型血友病患者的VII:CAg要么大致等于因子VIII凝血活性(VIII:C),要么VII:CAg无法检测到,这表明中度和轻度甲型血友病存在两种不同的分子机制。血清中可检测到VIII:CAg,但含量低于血浆。在2名血管性血友病患者中,VIII:CAg等于VII:C。1名血管性血友病患者输血后VIII:C的延迟增加伴随着VIII:CAg的轻微增加。胎儿血浆中含有可测量的VII:CAg。