Halpern S E, Tarburton J P, Sudora E, Hagan P
University of California, San Diego.
Eur J Nucl Med. 1992;19(6):387-93. doi: 10.1007/BF00177364.
This study was conducted to investigate alterations that occur in an indium/111 Fab' of a monoclonal antibody following its in vivo administration. Patients were infused with 111In-Fab' of the monoclonal antibody ZCE-025. Serum and urine specimens were collected from these patients. Starting materials, serum, urine and controls samples were studied by electrophoresis. Animal distribution studies were performed in normal Balb/c mice and, in some cases, nude mice bearing a carcinoembryonic antigen (CEA)/producing human colon tumour since the antibody targets CEA. The studies indicated that the molecule circulated almost totally intact for at least 4 h and to a considerable extent for 24 h, with some evidence for in vivo fragmentation by 24 h. Evidence was also obtained suggesting the formation of a high molecular weight species in some patients. Shortly after infusion, some of the 111In in the urine appeared as the intact Fab', but within hours the majority migrated electro-phoretically as low molecular weight species. We conclude that while the majority of the 111In-Fab' of this particular antibody remains intact and immunoreactive following its administration, the molecule is structurally changed to some degree shortly after its infusion into humans. Since each monoclonal antibody is unique, the degree and rapidity of degradation of its Fab' in vivo could vary markedly from the above and possibly adversely effect its utility as a radiopharmaceutical.
本研究旨在调查单克隆抗体的铟/111 Fab' 在体内给药后发生的变化。给患者输注单克隆抗体ZCE-025的111In-Fab'。从这些患者中采集血清和尿液样本。通过电泳研究起始材料、血清、尿液和对照样品。在正常Balb/c小鼠中进行动物分布研究,在某些情况下,在携带癌胚抗原(CEA)/产生人结肠肿瘤的裸鼠中进行,因为该抗体靶向CEA。研究表明,该分子在至少4小时内几乎完全完整地循环,在24小时内仍有相当程度的循环,有证据表明在24小时时发生了体内片段化。还获得了证据,表明在一些患者中形成了高分子量物质。输注后不久,尿液中的一些111In以完整的Fab'形式出现,但数小时内,大多数在电泳时迁移为低分子量物质。我们得出结论,虽然这种特定抗体的大多数111In-Fab'在给药后仍保持完整和免疫反应性,但该分子在注入人体后不久在结构上会发生一定程度的变化。由于每种单克隆抗体都是独特的,其Fab'在体内的降解程度和速度可能与上述情况有显著差异,并可能对其作为放射性药物的效用产生不利影响。