首页> 外文OA文献 >Recombinant ricin toxin A chain cytotoxicity against carcinoembryonic antigen expressing tumour cells mediated by a bispecific monoclonal antibody and its potentiation by ricin toxin B chain.
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Recombinant ricin toxin A chain cytotoxicity against carcinoembryonic antigen expressing tumour cells mediated by a bispecific monoclonal antibody and its potentiation by ricin toxin B chain.

机译:重组蓖麻毒蛋白A链对双特异性单克隆抗体介导的表达癌胚抗原的肿瘤细胞的细胞毒性及其由蓖麻毒蛋白B链的增强作用。

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摘要

A bispecific monoclonal antibody recognising both carcinoembryonic antigen (CEA) and ricin toxin A chain (RTA) was tested for its ability to target recombinant RTA (r-RTA) to CEA-expressing tumour cells, alone and in combination with ricin B chain (RTB). The antibody, 636 (Robins et al., 1990), induced significant RTA cytotoxicity against MKN45 gastric carcinoma cells which express high levels of CEA, using the r-RTA at a concentration below that known to be intrinsically cytotoxic. The addition of ricin toxin B chain (RTB) also potentiated cytotoxicity of r-RTA, and there was an additive increase in potentiation against CEA-positive cells when both RTB and 636 were included. The bispecific antibody restored potentiation by RTB after blocking of its binding site with excess galactose, and also the cytotoxic activity of whole ricin which had been blocked with galactose. It was concluded that the 636 bispecific antibody was highly effective in targeting the toxic moiety of the molecule to CEA-expressing cells, and allowed exploitation of the additional ability of the B chain to facilitate cellular incorporation. The facilitating function of the B chain was equally effective whether or not its lectin site was active.
机译:测试了识别癌胚抗原(CEA)和蓖麻毒素A链(RTA)的双特异性单克隆抗体将重组RTA(r-RTA)靶向表达CEA的肿瘤细胞的能力,可以单独使用,也可以与蓖麻毒素B链(RTB)结合使用)。使用r-RTA,其浓度低于已知的固有细胞毒性浓度,因此636抗体(Robins等,1990)对表达高水平CEA的MKN45胃癌细胞诱导了显着的RTA细胞毒性。蓖麻毒蛋白毒素B链(RTB)的添加也增强了r-RTA的细胞毒性,并且当同时包含RTB和636时,针对CEA阳性细胞的增强作用会增加。该双特异性抗体在用过量的半乳糖阻断其结合位点后恢复了RTB的增强作用,并且还用半乳糖阻断了整个蓖麻毒蛋白的细胞毒性。结论是,636双特异性抗体在将分子的毒性部分靶向表达CEA的细胞方面非常有效,并允许利用B链的其他能力来促进细胞掺入。无论其凝集素位点是否活跃,B链的促进功能都同样有效。

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