Brooks D A, Beckman I G, Bradley J, McNamara P J, Thomas M E, Zola H
J Immunol. 1981 Apr;126(4):1373-7.
The technique of somatic cell hybridization has been used to produce a monoclonal antibody (designated FMC7) against the human B lymphoblastoid cell line HRIK. By indirect immunofluorescence FMC7 reacted with a total of 3 out of 10 B cell lines, but failed to bind T and Null cell lines. On normal peripheral blood, FMC7 bound between 3 and 6% of mononuclear cells. When normal peripheral blood mononuclear cells were fractionated, FMC7 reacted with only the B-enriched fraction, staining some but not all cells expressing SMIg. Double marker analysis indicated that the antigen detected by FMC7 is not identical with any of the conventional B cell markers, including surface membrane IgM, C3 receptors, Fc receptors, and the binding site for mouse erythrocytes. Another monoclonal antibody, FMC1, which reacts specifically with B lymphocytes, binds a separate antigenic determinant. Thus, FMC7 appears to recognize a previously undetected marker present specifically on a subpopulation of human B lymphocytes. FMC7 reacts with some but not all B cell leukemias and may have diagnostic applications in leukemia.
体细胞杂交技术已被用于制备一种针对人B淋巴母细胞系HRIK的单克隆抗体(命名为FMC7)。通过间接免疫荧光法,FMC7与10个B细胞系中的3个发生反应,但不与T细胞系和裸细胞系结合。在正常外周血中,FMC7与3%至6%的单核细胞结合。当对正常外周血单核细胞进行分离时,FMC7仅与富含B细胞的部分发生反应,对一些但并非所有表达表面膜免疫球蛋白(SMIg)的细胞进行染色。双标记分析表明,FMC7检测到的抗原与任何传统B细胞标志物均不相同,包括表面膜免疫球蛋白M、C3受体、Fc受体以及小鼠红细胞结合位点。另一种单克隆抗体FMC1可特异性地与B淋巴细胞发生反应,它结合的是一个单独的抗原决定簇。因此,FMC7似乎识别出了一种先前未被检测到的标志物,该标志物特异性地存在于人类B淋巴细胞的一个亚群上。FMC7与部分而非所有的B细胞白血病发生反应,可能在白血病诊断中具有应用价值。