Debinski W, Karlsson B, Lindholm L, Siegall C B, Willingham M C, FitzGerald D, Pastan I
Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.
J Clin Invest. 1992 Aug;90(2):405-11. doi: 10.1172/JCI115875.
Two immunotoxins were constructed by chemically coupling the monoclonal antibody C242 to Pseudomonas exotoxin A (PE) or a modified form, NlysPE40, that lacks the cell binding domain of PE. Monoclonal antibody C242 recognizes a specific sialylated carbohydrate epitope on a high molecular weight membrane glycoprotein present on cells of human colon, pancreatic, and cervical cancers. C242-PE and C242-NlysPE40 were very cytotoxic for cells expressing this antigen with 50% inhibition of protein synthesis occurring on Colo205 cells at 0.2 ng/ml (0.9 pM) for C242-PE and 6.0 ng/ml (31 pM) for C242-NlysPE40. The two immunotoxins also exhibited a strong antitumor effect on a human colon cancer xenograft grown in nude mice. The specificity and potency of these two C242 immunotoxins warrant their further development for the treatment of cancer.
通过将单克隆抗体C242与绿脓杆菌外毒素A(PE)或缺乏PE细胞结合结构域的修饰形式NlysPE40进行化学偶联,构建了两种免疫毒素。单克隆抗体C242识别存在于人类结肠癌、胰腺癌和子宫颈癌细胞上的一种高分子量膜糖蛋白上的特定唾液酸化碳水化合物表位。C242-PE和C242-NlysPE40对表达该抗原的细胞具有很强的细胞毒性,对于C242-PE,在Colo205细胞上,当浓度为0.2 ng/ml(0.9 pM)时蛋白质合成受到50%的抑制,对于C242-NlysPE40,该浓度为6.0 ng/ml(31 pM)。这两种免疫毒素对裸鼠体内生长的人结肠癌异种移植瘤也表现出强烈的抗肿瘤作用。这两种C242免疫毒素的特异性和效力保证了它们在癌症治疗方面的进一步开发。