Griffiths R W, Gilham D E, Dangoor A, Ramani V, Clarke N W, Stern P L, Hawkins R E
Department of Medical Oncology, Paterson Institute for Cancer Research, Christie Research Centre, Manchester M20 4BX, UK.
Br J Cancer. 2005 Sep 19;93(6):670-7. doi: 10.1038/sj.bjc.6602776.
The 5T4 oncofoetal antigen is a heavily glycosylated cell surface protein found on human placental trophoblast and on diverse types of human cancer but is not expressed at significant levels on adult human tissues in health. It therefore satisfies the criteria for a tumour-associated antigen and is an ideal target for the immunotherapy of cancer. We report here that 5T4 is strongly expressed on the majority of renal cell carcinomas and therefore this population of patients is suitable for trials of 5T4-targeted therapies. In particular, we have shown that T cells from renal cell carcinoma patients can be genetically modified to kill 5T4 expressing renal cancer cell lines by introduction of a chimeric-signalling protein. This protein consists of a single chain antibody fragment capable of binding antigen directly at the cell surface and then activating the T cell by virtue of a CD3zeta-signalling domain. This is a powerful tool that bypasses a number of mechanisms that allow tumours to escape T-cell killing and can be readily scaled up for clinical use.
5T4癌胚抗原是一种高度糖基化的细胞表面蛋白,存在于人类胎盘滋养层细胞和多种类型的人类癌症中,但在健康的成体组织中表达水平不高。因此,它符合肿瘤相关抗原的标准,是癌症免疫治疗的理想靶点。我们在此报告,5T4在大多数肾细胞癌中强烈表达,因此这类患者适合进行5T4靶向治疗的试验。特别是,我们已经表明,通过引入嵌合信号蛋白,可以对肾细胞癌患者的T细胞进行基因改造,以杀死表达5T4的肾癌细胞系。这种蛋白由一个单链抗体片段组成,该片段能够直接在细胞表面结合抗原,然后通过CD3ζ信号域激活T细胞。这是一种强大的工具,绕过了许多使肿瘤逃避T细胞杀伤的机制,并且可以很容易地扩大规模用于临床。