Hathaway H S, Lubs M L, Kimberling W J, Hathaway W E
Pediatrics. 1976 Feb;57(2):251-4.
Rabbit antibody to purified human factor VIII was prepared and absorbed until it formed only one precipitin line against normal and hemophilic plasmas and no line against severe von Willebrand's disease plasma. The plasma protein which combines with this rabbit antibody to factor VIII is referred to as factor VIII antigen. The ratio of percent factor VIII activity (by coagulation assay) to percent factor VIII antigen was used for carrier detection. Thirty-seven normal women, 33 obligate carriers, 12 probable carriers, and 39 possible carriers, were studied by this technique. Using the ratio of 0.84 as the division between normals and carriers, 31 of the 33 carriers (91%) were classified carriers. Twenty of the 39 possible carriers were classified as carriers (51%) and ten of the 12 probable carriers were positively identified. The results of discriminate analysis of all three variables (VIII activity, VIII antigen, and the ratio of VIII activity to VIII antigen indicated that the discrimination power of the ratio alone could not be improved by introducing the other variables on this set of data. These findings confirm the usefulness of the VIII activity to VIII antigen ratio in the detection of carriers of classical hemophilia.
制备了针对纯化人因子VIII的兔抗体,并进行吸收处理,直至其仅与正常血浆和血友病血浆形成一条沉淀线,而与重度血管性血友病血浆不形成沉淀线。与该兔抗因子VIII抗体结合的血浆蛋白被称为因子VIII抗原。采用因子VIII活性百分比(通过凝血测定)与因子VIII抗原百分比的比值来进行携带者检测。运用该技术对37名正常女性、33名肯定携带者、12名可能携带者和39名疑似携带者进行了研究。以0.84作为正常人与携带者的划分比值,33名携带者中有31名(91%)被归类为携带者。39名疑似携带者中有20名被归类为携带者(51%),12名可能携带者中有10名被明确鉴定为携带者。对所有三个变量(VIII活性、VIII抗原以及VIII活性与VIII抗原的比值)进行判别分析的结果表明,在这组数据中,仅引入其他变量并不能提高比值本身的判别能力。这些发现证实了VIII活性与VIII抗原比值在检测经典血友病携带者中的有用性。