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作 者:梁福佑[1] 张胜华[1] 潘颖[1] 徐琳娜[1] 王维刚[1]
机构地区:[1]首都医科大学细胞生物学研究室 [2]中国医学科学院中国协和医科大学医药生物技术研究所
出 处:《首都医科大学学报》1999年第1期5-8,共4页Journal of Capital Medical University
基 金:北京市自然科学基金
摘 要:用单抗3A5制备与去甲斑蝥素(NCTD)的偶联物。ELISA检测结果表明:3A5NCTD偶联物保持对人肝癌BEL7402细胞的免疫反应性。克隆生成法测定结果显示:3A5NCTD具有比NCTD更强的细胞毒性,两者的IC50分别为2.3mg/L和4.2mg/L。小鼠腹腔内移植H22肝癌,腹膜内给药(ip),3A5NCTD(3mg/kg)和NCTD(3mg/kg)的延长寿命值(ILS)分别为168%和42%。裸鼠移植人肝癌BEL7402细胞,静脉给药(iv),NCTD的肿瘤抑制率为15%(P>0.05),3A5NCTD为62%(P<0.01);瘤结周围给药(pt),NCTD的肿瘤抑制率为47%(P<0.05),3A5NCTD为78%(P<0.01)。结果表明,与NCTD相比,3A5NCTD对裸鼠移植人肝癌和腹腔肿瘤具有更强的治疗作用。以上结果提示单抗与NCTD偶联物在肿瘤的导向治疗中有较好的疗效。A rat monoclonal antibody was linked to norcantharidin (NCTD), an antitumor drug currently in clinical use McAb 3A5. The 3A5 NCTD conjugate retained complete immunoreactivity of McAb 3A5 to human hepatoma cancer BEL 7402 cells. The IC 50 values of 3A5 NCTD and free NCTD were 2.3 mg/L and 4.2 mg/L, respectively. The 3A5 NCTD showed higher cytotoxicity than free NCTD. Hepatoma H22 ascites was transplanted into the peritoneal of mice. 3A5 NCTD or NCTD were injected into the cavity. The ILS(%) values were 168% and 42%. Tumor fragments of human hepatoma BEL 7402 were transplanted into nude mice. Then 3A5 NCTD or NCTD was injected iv, or pt(peritumorally). The inhibition rates on the growth of hepatoma BEL 7402 xenografts were 62% and 15% for iv; 78% and 47% for pt.Results indicate that 3A5 NCTD is highly effective against targeted human cancer xenograft and mouse tumor.
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