Singh M, Ghose T, Mezei M, Belitsky P
School of Pharmacy, Dalhousie University, Halifax, Nova Scotia, Canada.
Cancer Lett. 1991 Feb;56(2):97-102. doi: 10.1016/0304-3835(91)90082-s.
The monoclonal antibody DAL K29 against a human renal cell carcinoma associated cell surface antigen was covalently linked to small unilamellar lipid vesicles (SUV) containing the antifolate, methotrexate (MTX), with full retention of antibody activity. In an ascites tumor model developed after intraperitoneal inoculation of 5 x 10(6) cells of the human kidney cancer line Caki-1 per pristane primed nude mouse, the DAL K29 linked MTX-containing SUV was a more potent tumor inhibitor (P less than 0.0005) than the drug or MAB alone, MTX-containing SUV, a mixture of DAL K29 and MTX-containing SUV or MTX-containing SUV linked to an isotype matched nontumor specific IgG.
针对一种人肾细胞癌相关细胞表面抗原的单克隆抗体DAL K29与含有抗叶酸剂甲氨蝶呤(MTX)的小单层脂质囊泡(SUV)共价连接,抗体活性完全保留。在每只经普氏烷预处理的裸鼠腹腔接种5×10⁶人肾癌Caki-1细胞系细胞后建立的腹水肿瘤模型中,与单独的药物或单克隆抗体、含MTX的SUV、DAL K29和含MTX的SUV的混合物或与同型匹配的非肿瘤特异性IgG连接的含MTX的SUV相比,连接了DAL K29的含MTX的SUV是一种更有效的肿瘤抑制剂(P<0.0005)。