Gingrich R D, Dahle C E, Hoskins K F, Senneff M J
University of Iowa College of Medicine, Iowa City.
Blood. 1990 Jun 15;75(12):2375-87.
A monoclonal antibody, 1D10, was derived that identifies a new antigenic epitope on the surface of malignant B lymphocytes. Normal resting and stimulated lymphocytes do not express the antigen. The majority of individuals with acute Epstein-Barr virus infection express the antigen on their lymphocytes, and in these patients, the T lymphocyte may also be antigen positive. The antigen was found on B-lymphoid neoplasia from the early pre-B cell stage through terminally differentiated plasma cells, a characteristic not reported for other B cell-associated antigens. Studies on homozygous typing cells and cells from individuals with known HLA phenotypes indicate that the antigen does not segregate in a pattern characteristic for major histocompatibility antigens. The molecule is a heterodimeric polypeptide with the molecular weight and isoelectric points of the alpha and beta chains being 32,000 d/4 and 28,000 d/6, respectively. Evidence is presented that the 1D10 molecule is not HLA-DR, -DP, or -DQ. By extrapolation, we suggest that this novel molecule may represent HLA D-region gene expression of a gene(s) not normally expressed. Potential candidates are D-region pseudogenes. We conclude that the antigenic epitope identified by the 1D10 monoclonal antibody is unique among previously described B-lymphocyte antigens. Further studies of the factors controlling the expression of this molecule, as well as studies designed to look at the possible cellular function, may provide insights for understanding crucial events in the malignant transformation of lymphocytes.
一种单克隆抗体1D10被研制出来,它可识别恶性B淋巴细胞表面的一个新抗原表位。正常静止和受刺激的淋巴细胞不表达该抗原。大多数急性爱泼斯坦-巴尔病毒感染个体的淋巴细胞表达该抗原,在这些患者中,T淋巴细胞也可能呈抗原阳性。在从早期前B细胞阶段到终末分化浆细胞的B淋巴细胞肿瘤中发现了该抗原,这是其他B细胞相关抗原未报道的特征。对纯合分型细胞和已知HLA表型个体的细胞研究表明,该抗原不以主要组织相容性抗原的特征模式进行分离。该分子是一种异二聚体多肽,α链和β链的分子量和等电点分别为32,000 d/4和28,000 d/6。有证据表明1D10分子不是HLA-DR、-DP或-DQ。由此推断,我们认为这种新分子可能代表一个通常不表达的基因的HLA D区基因表达。潜在的候选基因是D区假基因。我们得出结论,1D10单克隆抗体识别的抗原表位在先前描述的B淋巴细胞抗原中是独特的。对控制该分子表达的因素的进一步研究,以及旨在研究其可能的细胞功能的研究,可能为理解淋巴细胞恶性转化中的关键事件提供见解。