Griffiths L, Binley K, Iqball S, Kan O, Maxwell P, Ratcliffe P, Lewis C, Harris A, Kingsman S, Naylor S
Oxford BioMedica (UK) Ltd, Oxford, UK.
Gene Ther. 2000 Feb;7(3):255-62. doi: 10.1038/sj.gt.3301058.
The use of activated macrophages in the treatment of cancer has been largely ineffectual. By 'arming' these cells with the ability to express a therapeutic gene we demonstrate significant advances in the efficacy of this approach. We have used a hypoxia-regulated adenoviral vector to transduce human macrophages with either a reporter or a therapeutic gene encoding human cytochrome P4502B6 (CYP2B6). Infiltration of transduced macrophages into a tumour spheroid results in induction of gene expression. We demonstrate significant tumour cell killing only in the presence of cyclophosphamide via activation by P4502B6 and show that this can be further targeted to tumours through hypoxia regulated gene expression. Gene Therapy (2000) 7, 255-262.
活化巨噬细胞在癌症治疗中的应用大多没有效果。通过赋予这些细胞表达治疗性基因的能力,我们证明了这种方法在疗效上有显著进展。我们使用了一种缺氧调节腺病毒载体,用编码人细胞色素P4502B6(CYP2B6)的报告基因或治疗性基因转导人巨噬细胞。转导的巨噬细胞浸润到肿瘤球体中会导致基因表达的诱导。我们仅在环磷酰胺存在的情况下,通过P4502B6激活证明了显著的肿瘤细胞杀伤作用,并表明这可以通过缺氧调节基因表达进一步靶向肿瘤。《基因治疗》(2000年)7卷,第255 - 262页 。