Ohkawa K, Tsukada Y, Hibi N, Umemoto N, Hara T
Cancer Immunol Immunother. 1986;23(2):81-6. doi: 10.1007/BF00199811.
The anticancer drug mitomycin C (MMC) was conjugated with an affinity-purified horse antibody to human alpha-fetoprotein (aAFP) with human serum albumin (HSA) as the intermediate drug carrier. The conjugate (aAFP:HSA:MMC molar ratio, 1:1:30) retained full antibody binding activity as determined by a competitive binding radioimmunoassay. In a cytotoxicity test in which the AFP-producing human yolk sac tumor TG-1 cells were preincubated with test materials for 2 h followed by an additional 48-h culture in fresh medium, the conjugate was 20-fold more cytotoxic than free MMC at an equivalent MMC concentration of 100 ng/ml. The in vivo antitumor effect of the conjugate was tested against the human yolk sac tumor JOG-9 growing in athymic nude mice. When the tumor-bearing mice were treated with a total of 6 injections given on 2 consecutive days and then every other day starting 8 days after SC tumor inoculation [2 (equivalent MMC) microgram/head per injection], the conjugate retarded tumor growth more effectively than free MMC and normal horse immunoglobulin conjugate.
抗癌药物丝裂霉素C(MMC)通过人血清白蛋白(HSA)作为中间药物载体与亲和纯化的抗人甲胎蛋白(aAFP)马抗体结合。通过竞争性结合放射免疫测定法确定,该结合物(aAFP:HSA:MMC摩尔比为1:1:30)保留了完整的抗体结合活性。在一项细胞毒性试验中,将产生甲胎蛋白的人卵黄囊瘤TG-1细胞与测试材料预孵育2小时,然后在新鲜培养基中再培养48小时,在MMC等效浓度为100 ng/ml时,该结合物的细胞毒性比游离MMC高20倍。在无胸腺裸鼠体内对人卵黄囊瘤JOG-9进行了结合物的抗肿瘤效果测试。当荷瘤小鼠在皮下接种肿瘤8天后,连续2天每天注射共6次,然后每隔一天注射一次[每次注射2(等效MMC)微克/只],该结合物比游离MMC和正常马免疫球蛋白结合物更有效地抑制肿瘤生长。