Kovarík J, Bártek J, Lauerová L, Munzarová M
Neoplasma. 1984;31(1):75-8.
Hybridoma clones were established by fusing spleen cells from mice hyperimmunized with human breast cancer cells of MDA-MB-231 line with murine myeloma cells P3-X63-Ag8-653. Ten permanent hybridomas were stabilized. The monoclonal antibodies of three of them, i.e. HBCA-6, HBCA-4 and HBCA-12 were tested against 20 various established cell lines. The most restricted binding properties showed HBCA-12 antibody which reacted positively only with two types of target cells. The cross-reactivity of HBCA-12 with human breast cancer cell line MDA-MB-231 and human myeloma derived cells ARH-77 is discussed in view of the pertinent target structure, i.e. differentiation antigens, allospecific antigens, hormone receptors and shared tumor associated antigens. It was shown that the target structure for HBCA-12 is localized on the cell surface.
通过将用MDA - MB - 231系人乳腺癌细胞超免疫的小鼠脾细胞与鼠骨髓瘤细胞P3 - X63 - Ag8 - 653融合,建立了杂交瘤克隆。十个永久性杂交瘤得以稳定。其中三个杂交瘤产生的单克隆抗体,即HBCA - 6、HBCA - 4和HBCA - 12,针对20种不同的已建立细胞系进行了测试。HBCA - 12抗体表现出最具特异性的结合特性,仅与两种类型的靶细胞呈阳性反应。鉴于相关的靶结构,即分化抗原、同种特异性抗原、激素受体和共同的肿瘤相关抗原,讨论了HBCA - 12与人乳腺癌细胞系MDA - MB - 231和人骨髓瘤衍生细胞ARH - 77的交叉反应性。结果表明,HBCA - 12的靶结构定位于细胞表面。