Beaumier P L, Neuzil D, Yang H M, Noll E A, Kishore R, Eary J F, Krohn K A, Nelp W B, Hellström K E, Hellström I
J Nucl Med. 1986 Jun;27(6):824-8.
A convenient, rapid, and reproducible assay was developed to evaluate the immunoreactivity of radiolabeled monoclonal antibodies against three different human melanoma-associated antigens, p97, a proteoglycan and a GD3 ganglioside. A cloned melanoma cell line (M 2669 CL 13) was selected as the target and, when fixed with paraformaldehyde, showed binding as good as or better than that obtained with live cells for the three antigens. Fixed cells retained good binding properties stored at 4 degrees C for over 6 mo. This assay has general applicability to other antigen-antibody systems for testing chemically modified monoclonal antibodies or fragments during the development of a radiopharmaceutical or as a routine quality control measure for clinical agents.
开发了一种简便、快速且可重复的检测方法,用于评估放射性标记的单克隆抗体针对三种不同的人类黑色素瘤相关抗原(p97、一种蛋白聚糖和一种GD3神经节苷脂)的免疫反应性。选择一种克隆的黑色素瘤细胞系(M 2669 CL 13)作为靶标,用多聚甲醛固定后,对于这三种抗原,其显示出与活细胞相当或更好的结合效果。固定后的细胞在4℃储存超过6个月仍保持良好的结合特性。该检测方法普遍适用于其他抗原-抗体系统,用于在放射性药物开发过程中检测化学修饰的单克隆抗体或片段,或作为临床制剂的常规质量控制措施。