Kalafut F, Kusenda J, Novotná L, Cernák A
Cancer Research Institute, Slovak Academy of Sciences, Bratislava, Czechoslovakia.
Neoplasma. 1987;34(6):693-701.
Mouse Sp2/10 myeloma cells were fused with spleen cells from mice that had been immunized with freshly obtained primary human uveal melanoma cells. Hybrids that produced antibodies binding to the uveal melanoma cells, but not to fibroblasts, uveal or retinal cells of healthy donors, were cloned. Extensive specificity tests showed that the antibodies produced by the ten clones bound strongly to fresh or short-time cultures of primary human uveal melanoma tumor cells (UMEL-H, UMEL-K). Weaker binding occurred with a human uveal melanoma cell line (VUP-1), and with human skin melanoma cell lines (HMB-2, B-HM8), respectively. Binding assays with carcinoma cells, fibroblasts, uveal and retinal cells were negative. An intensive screening of this type is now under way.
将小鼠Sp2/10骨髓瘤细胞与用新鲜获取的原发性人葡萄膜黑色素瘤细胞免疫的小鼠脾细胞进行融合。克隆出能产生与葡萄膜黑色素瘤细胞结合但不与健康供体的成纤维细胞、葡萄膜或视网膜细胞结合的抗体的杂交细胞。广泛的特异性测试表明,十个克隆产生的抗体与原发性人葡萄膜黑色素瘤肿瘤细胞(UMEL-H、UMEL-K)的新鲜或短期培养物强烈结合。与人类葡萄膜黑色素瘤细胞系(VUP-1)以及人类皮肤黑色素瘤细胞系(HMB-2、B-HM8)的结合较弱。与癌细胞、成纤维细胞、葡萄膜和视网膜细胞的结合试验均为阴性。目前正在进行这种类型的深入筛选。