Garnett M C, Embleton M J, Jacobs E, Baldwin R W
Int J Cancer. 1983 May 15;31(5):661-70. doi: 10.1002/ijc.2910310520.
The preparation and properties of a drug-carrier-antibody preparation are reported. The antifolate chemotherapeutic agent methotrexate was covalently coupled to human serum albumin as a carrier. The carrier-drug preparation was then chemically linked to a monoclonal antibody, raised originally against a human osteogenic sarcoma cell line, 791T, in a manner permitting retention of antibody-binding activity. The cytotoxic properties of the conjugate were tested in vitro in comparison with carrier-methotrexate and free methotrexate against a panel of tumour cell lines containing both antigenically cross-reactive cell lines and cell lines having low antigenic cross-reactivity with the monoclonal antibody. The cytotoxicity tests demonstrated that coupling of methotrexate to carrier caused a loss of some drug activity but that coupling of the antibody to the carrier-drug preparation permitted full expression of drug cytotoxicity against antibody-reactive cell lines. It was further demonstrated that the conjugate was selective in its action and was preferentially cytotoxic towards antibody-reactive cell types. The cytotoxicity against antibody-reactive cell lines was shown by competitive inhibition by free antibody to be entirely dependent on antibody binding. A clonogenic assay showed that the conjugate was capable of killing greater than 99% of 791T target cells. These results indicate that a drug-carrier antibody conjugate can be synthesized which has all the in vitro properties theoretically necessary for a successful antibody-targeted cytotoxic agent.
报道了一种药物-载体-抗体制剂的制备及其性质。抗叶酸化疗药物甲氨蝶呤被共价偶联到人血清白蛋白作为载体。然后将载体-药物制剂化学连接到一种单克隆抗体上,该单克隆抗体最初是针对人骨肉瘤细胞系791T产生的,连接方式能保留抗体结合活性。将该缀合物的细胞毒性性质与载体-甲氨蝶呤和游离甲氨蝶呤在体外针对一组肿瘤细胞系进行了测试,这些细胞系既包含抗原交叉反应性细胞系,也包含与单克隆抗体抗原交叉反应性低的细胞系。细胞毒性测试表明,甲氨蝶呤与载体偶联导致了一些药物活性的丧失,但抗体与载体-药物制剂偶联使药物对抗体反应性细胞系的细胞毒性得以充分表达。进一步证明该缀合物作用具有选择性,对抗体反应性细胞类型具有优先细胞毒性。游离抗体的竞争性抑制表明,对抗体反应性细胞系的细胞毒性完全依赖于抗体结合。克隆形成试验表明,该缀合物能够杀死超过99%的791T靶细胞。这些结果表明,可以合成一种药物-载体-抗体缀合物,其具有理论上作为成功的抗体靶向细胞毒性剂所需的所有体外性质。