首页> 美国卫生研究院文献>The British Journal of Cancer. Supplement >Monoclonal antibodies recognising the cluster 2 antigen associated with human small cell lung cancer mediate the toxic effects of ricin A chain in an indirect assay of immunotoxin cytotoxicity.
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Monoclonal antibodies recognising the cluster 2 antigen associated with human small cell lung cancer mediate the toxic effects of ricin A chain in an indirect assay of immunotoxin cytotoxicity.

机译:在免疫毒素细胞毒性的间接测定中识别与人类小细胞肺癌相关的簇2抗原的单克隆抗体介导蓖麻毒蛋白A链的毒性作用。

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摘要

Monoclonal antibodies (Mabs) submitted to the Second International Workshop on Small Cell Lung Cancer Antigens were screened for their ability to mediate the toxic effects of ricin A chain against the NCI-H69 cell line in an indirect assay of immunotoxin cytotoxicity. Cluster 1 Mabs, recognising the neural cell adhesion molecule, mediated little or no cytotoxic effect in combination with screening agent, ricin A chain linked to an antibody Fab' fragment recognising either mouse or rat Mabs. In contrast, cluster 2 Mabs, recognising an epithelial tumour-associated antigen, generally mediated potent cytotoxic effects with the screening agent, inhibiting the incorporation of 3H-leucine by NCI-H69 cells by between 90% and 99%. Measurements of Mab binding to the NCI-H69 cell line by indirect immunofluorescence and flow cytometry indicated that the cluster 2 Mabs generally bound in higher amounts than the cluster 1 Mabs suggesting that the cluster 1 Mabs were ineffective in the screen because they did not bind to the cells in sufficient amounts. However, Mabs recognising antigens other than cluster 1 bound to NCI-H69 cells in amounts similar to those of the cluster 2 Mabs yet did not mediate potent cytotoxic effects in the indirect assay suggesting that the cluster 2 antigen may be internalised in a fashion favouring the delivery of ricin A chain to the cytosol.
机译:在免疫毒素细胞毒性的间接测定中,筛选了提交给第二届小细胞肺癌国际研讨会的单克隆抗体(Mabs),以介导蓖麻毒素A链对NCI-H69细胞系的毒性作用的能力。与识别剂,蓖麻毒素A链结合识别神经细胞粘附分子的簇1单克隆抗体介导的细胞毒性作用很小或没有介导的细胞毒作用,该链素与识别小鼠或大鼠单克隆抗体的抗体Fab'片段相连。相反,识别出上皮肿瘤相关抗原的簇2单克隆抗体通常用筛选剂介导有效的细胞毒性作用,将NCI-H69细胞掺入3H-亮氨酸的程度在90%至99%之间。通过间接免疫荧光和流式细胞术测量的单克隆抗体与NCI-H69细胞系的结合表明,簇2 Mab的结合量通常高于簇1 Mab,这表明簇1 Mab在筛选中无效,因为它们未结合足够数量的细胞。但是,单克隆抗体识别的簇1以外的抗原与NCI-H69细胞结合的量与簇2 Mab相似,但在间接测定中并未介导强的细胞毒性作用,这表明簇2抗原可能以有利于内源性的方式被内在化。蓖麻毒蛋白A链传递到细胞质。

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