Moulds J M, Nickells M W, Moulds J J, Brown M C, Atkinson J P
Howard Hughes Medical Institute Laboratory, Washington University School of Medicine, St. Louis, Missouri 63110.
J Exp Med. 1991 May 1;173(5):1159-63. doi: 10.1084/jem.173.5.1159.
Erythrocytes (E) lacking high incidence blood group antigens were screened by an antiglobulin test with a monoclonal antibody to human complement receptor type 1 (CR1; C3b/C4b receptor; CD35). Some examples of E lacking Knops, McCoy, Swain-Langley, and York antigens, a serologically related group, were not agglutinated. Moreover, E of the null phenotype for these same antigens were nonreactive. To further explore this relationship, E expressing these antigens were surface labeled, solubilized, and incubated with the corresponding blood group-specific antisera. CR1 was immunoprecipitated, indicating that the epitopes recognized by each of these antisera are expressed on CR1. E of two individuals, putative null phenotypes for the Knops, McCoy, and Swain-Langley blood group antigens, expressed a very low number of CR1 (less than 30/E; approximately 10% of the normal mean). This observation accounts for their lack of reactivity in the antiglobulin test and their prior designation as null phenotypes. Also, the previously reported low as well as variable expression of CR1 on E explains prior difficulties in the serologic analyses of these blood group antigens.
通过使用针对人补体受体1(CR1;C3b/C4b受体;CD35)的单克隆抗体进行抗球蛋白试验,筛选缺乏高频率血型抗原的红细胞(E)。一些缺乏诺普斯、麦科伊、斯温-兰利和约克抗原(一个血清学相关组)的红细胞样本未发生凝集。此外,这些相同抗原的零表型红细胞不发生反应。为了进一步探究这种关系,对表达这些抗原的红细胞进行表面标记、溶解,并与相应的血型特异性抗血清孵育。CR1被免疫沉淀,表明这些抗血清识别的表位在CR1上表达。两名个体的红细胞,推测为诺普斯、麦科伊和斯温-兰利血型抗原的零表型,表达的CR1数量非常少(每个红细胞少于30个;约为正常平均值的10%)。这一观察结果解释了它们在抗球蛋白试验中缺乏反应性以及之前被指定为零表型的原因。此外,先前报道的红细胞上CR1的低表达以及表达的变异性解释了这些血型抗原血清学分析中先前遇到的困难。