Rebaï N, Malissen B
Tissue Antigens. 1983 Aug;22(2):107-17. doi: 10.1111/j.1399-0039.1983.tb01176.x.
The monoclonal antibodies B1.23.2 and B9.12 were developed to characterize human class I major histocompatibility gene products. They detect two different epitopes and define on a given lymphoblastoid B cell line two subsets of beta 2 microglobulin-complexed HLA class I molecules. One subset reacts with B9.12 and B1.23.2 and the other one expresses only the B9.12 epitope. Binding assays were performed on C3H mouse L cells which had been transformed with various single HLA-class I genes and the two detected molecular subsets were shown to be encoded by different genetic loci. Unlike B1.23.2, B9.12 detects all the beta 2m-complexed molecules expressed in human B cell lines and recognizes an epitope different from the one defined by W6/32. In contrast to the vast majority of the other reported anti-class I monoclonal antibodies (including B9.12), B1.23.2 recognizes an epitope expressed on both beta 2m-associated and -free HLA class I heavy chains.
单克隆抗体B1.23.2和B9.12用于鉴定人类I类主要组织相容性基因产物。它们可检测两种不同的表位,并在给定的淋巴母细胞性B细胞系上定义了两个与β2微球蛋白复合的HLA I类分子亚群。一个亚群与B9.12和B1.23.2发生反应,另一个亚群仅表达B9.12表位。对用各种单个HLA I类基因转化的C3H小鼠L细胞进行了结合试验,结果表明这两个检测到的分子亚群由不同的基因座编码。与B1.23.2不同,B9.12可检测人类B细胞系中表达的所有与β2m复合的分子,并识别一个与W6/32定义的表位不同的表位。与绝大多数其他报道的抗I类单克隆抗体(包括B9.12)不同,B1.23.2识别在与β2m相关和游离的HLA I类重链上均表达的一个表位。