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通过人血清白蛋白与丝裂霉素C偶联的抗人甲胎蛋白纯化抗体对人卵黄囊瘤细胞系进行体外和体内选择性生长抑制。

Selective in vitro and in vivo growth inhibition against human yolk sac tumor cell lines by purified antibody against human alpha-fetoprotein conjugated with mitomycin C via human serum albumin.

作者信息

Ohkawa K, Tsukada Y, Hibi N, Umemoto N, Hara T

出版信息

Cancer Immunol Immunother. 1986;23(2):81-6. doi: 10.1007/BF00199811.

Abstract

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.

摘要

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。

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