Schlapfer P, Nydegger T, Bütler-Brunner E, Morgenthaler J J, Bütler R, Blaser K
Laboratory of Molecular Immunology, University of Berne, Switzerland.
Hybridoma. 1987 Dec;6(6):575-88. doi: 10.1089/hyb.1987.6.575.
Human low density lipoprotein shows a genetic polymorphism, the so-called Ag-system. it consists of 5 pairs of allelic epitopes, x/y, al/d, c/g, t/z, and h/i, which are localized on apolipoprotein B. We have generated a large number of monoclonal antibodies against low density lipoprotein. Two of them, D2E1 and H11G3, recognize epitopes related to this genetic polymorphism. Direct ELISA and ELISA inhibition experiments with different low density lipoproteins of known phenotype showed that D2E1 is directed against the allelic epitope c and H11G3 against d. The two antibodies were used for the characterization of low density lipoprotein in sera from different blood donors and the results compared to those obtained by passive hemagglutination using human allotypic anti-sera. Sera from homo- or heterozygous donors (which display the relevant epitope) could be distinguished from the sera of homozygous donors (which lack the epitope) with the monoclonal antibodies described.
人类低密度脂蛋白表现出一种遗传多态性,即所谓的Ag系统。它由5对等位基因表位组成,x/y、al/d、c/g、t/z和h/i,这些表位位于载脂蛋白B上。我们已经产生了大量针对低密度脂蛋白的单克隆抗体。其中两种,D2E1和H11G3,识别与这种遗传多态性相关的表位。用已知表型的不同低密度脂蛋白进行直接ELISA和ELISA抑制实验表明,D2E1针对等位基因表位c,H11G3针对d。这两种抗体用于表征不同献血者血清中的低密度脂蛋白,并将结果与使用人同种异型抗血清通过被动血凝试验获得的结果进行比较。使用所述单克隆抗体,可以将来自纯合或杂合供体(显示相关表位)的血清与纯合供体(缺乏该表位)的血清区分开来。