Cornetta K, Croop J, Dropcho E, Abonour R, Kieran M W, Kreissman S, Reeves L, Erickson L C, Williams D A
Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, 46202, USA.
Cancer Gene Ther. 2006 Sep;13(9):886-95. doi: 10.1038/sj.cgt.7700963. Epub 2006 Apr 28.
Administration of chemotherapy is often limited by myelosuppression. Expression of drug-resistance genes in hematopoietic cells has been proposed as a means to decrease the toxicity of cytotoxic agents. In this pilot study, we utilized a retroviral vector expressing methylguanine DNA methyltransferase (MGMT) to transduce hematopoietic progenitors, which were subsequently used in the setting of alkylator therapy (procarbazine, CCNU, vincristine (PCV)) for poor prognosis brain tumors. Granulocyte colony-stimulating factor (G-CSF)-mobilized peripheral blood progenitor cells were collected by apheresis and enriched for CD34+ expression. Nine subjects were infused with CD34+-enriched cells treated in a transduction procedure involving a 4-day exposure to cytokines with vector exposure on days 3 and 4. No major adverse event was related to the gene therapy procedure. Importantly, the engraftment kinetics of the treated product was similar to unmanipulated peripheral blood stem cells, suggesting that the ex vivo manipulation did not significantly reduce engrafting progenitor cell function. Gene-transduced cells were detected in all subjects. Although the level and duration was limited, patients receiving cells transduced using fibronectin 'preloaded' with virus supernatant appeared to show improved in vivo marking frequency. These findings demonstrate the feasibility and safety of utilizing MGMT-transduced CD34+ peripheral blood progenitor cells in the setting of chemotherapy.
化疗的应用常常受到骨髓抑制的限制。有人提出在造血细胞中表达耐药基因作为降低细胞毒性药物毒性的一种方法。在这项初步研究中,我们利用一种表达甲基鸟嘌呤DNA甲基转移酶(MGMT)的逆转录病毒载体转导造血祖细胞,随后将其用于预后不良的脑肿瘤的烷化剂治疗(丙卡巴肼、洛莫司汀、长春新碱(PCV))。通过单采术收集粒细胞集落刺激因子(G-CSF)动员的外周血祖细胞,并富集CD34+表达。9名受试者输注了经转导程序处理的富含CD34+的细胞,该程序包括在第3天和第4天暴露于细胞因子并同时暴露于载体,为期4天。没有重大不良事件与基因治疗程序相关。重要的是,处理后的产物的植入动力学与未处理的外周血干细胞相似,这表明体外操作并没有显著降低植入祖细胞的功能。在所有受试者中都检测到了基因转导细胞。尽管水平和持续时间有限,但接受用病毒上清液“预加载”纤连蛋白转导的细胞的患者似乎显示出体内标记频率有所提高。这些发现证明了在化疗中利用MGMT转导的CD34+外周血祖细胞的可行性和安全性。