Ratnoff O D, Jones P K
Am J Clin Pathol. 1976 Feb;65(2):129-35. doi: 10.1093/ajcp/65.2.129.
The authors summarize their experience with detection of the carrier state in classic hemophilia. Their test depends upon the observation that the plasma of patients with classic hemophilia, deficient in functional antihemophilic factor, contains normal amounts of precipitating antigenic material. By inference, the plasma of carriers should be relatively deficient in functional antihemophilic factor, but should contain normal amounts of antihemophilic factor-like antigenic material. Data obtained from 81 obligate carriers suggest that at least 90% of these women can be identified as carriers in the laboratory by demonstrating that there is an excess of antihemophilic factor-like antigenic material in plasma relative to functional antihemophilic factor. Further, at least two-thirds of mothers of individuals with isolated cases of hemophilia are carriers, suggesting that mutation is a relatively rare cause of hemophilia. Only about one-third of daughters of carriers who had no sons can be identified as carriers, a result due to the systematic exclusion of those daughters who had already had a hemophilic son.
作者总结了他们在检测典型血友病携带者状态方面的经验。他们的检测基于这样的观察:典型血友病患者的血浆中缺乏功能性抗血友病因子,但含有正常量的沉淀抗原物质。由此推断,携带者的血浆中功能性抗血友病因子应相对缺乏,但应含有正常量的抗血友病因子样抗原物质。从81名确定的携带者获得的数据表明,通过证明血浆中抗血友病因子样抗原物质相对于功能性抗血友病因子过量,至少90%的这些女性在实验室中可被鉴定为携带者。此外,散发性血友病患者的母亲中至少三分之二是携带者,这表明突变是血友病相对罕见的病因。没有儿子的携带者女儿中只有约三分之一可被鉴定为携带者,这一结果是由于已生育血友病儿子的女儿被系统排除在外。