Luo H Y, Clarke B J, Gauldie J, Patterson M, Liao S K, Chui D H
Department of Pathology, McMaster University School of Medicine, Hamilton, Ontario, Canada.
Blood. 1988 Nov;72(5):1589-94.
The presence of minute amounts of embryonic zeta-globin chains in adult hemolysates is a marker for carriers of alpha-thalassemia-1 resulting from (--SEA/) deletion. Recently, we developed a murine monoclonal antihuman embryonic zeta-globin chain antibody, 8E8. By using this antibody, we have now established a slot-blot immunobinding assay for the rapid detection of zeta-globin chains in adult hemolysates. zeta-globin chains were found to be present in 30 blood samples obtained from individuals who were carriers of alpha-thalassemia-1. In another 30 blood samples from individuals who were not carriers of the (--SEA/) deletion, zeta-globin chains were not detected. This simple diagnostic test can be used in appropriate populations to identify those couples at risk of conceiving fetuses afflicted with the Hb Bart's hydrops fetalis syndrome due to homozygous alpha-thalassemia.
成人溶血产物中存在微量胚胎型ζ-珠蛋白链是由(--SEA/)缺失导致的α地中海贫血-1携带者的一个标志物。最近,我们研制出一种鼠单克隆抗人胚胎型ζ-珠蛋白链抗体8E8。利用该抗体,我们现已建立一种斑点印迹免疫结合测定法,用于快速检测成人溶血产物中的ζ-珠蛋白链。在从α地中海贫血-1携带者获取的30份血样中发现存在ζ-珠蛋白链。在另外30份来自非(--SEA/)缺失携带者个体的血样中,未检测到ζ-珠蛋白链。这种简单的诊断测试可用于合适的人群,以识别那些有生育因纯合α地中海贫血而患巴氏水肿胎儿综合征胎儿风险的夫妇。