Kohn D B
Department of Pediatrics, University of Southern California School of Medicine, Children's Hospital, Los Angeles 90027, USA.
Curr Opin Mol Ther. 1999 Aug;1(4):437-42.
While gene therapy using hematopoietic stem cells was the first area of investigation in the field, success has proven elusive. However, significant progress has been achieved recently in methods for more effective gene transfer and expression. In addition to greatly improved results using retroviral vectors, adeno-associated vectors and lentiviral vectors appear to be promising for stable transduction of hematopoietic stem cells. These advances, documented in animal transplant models, are now being applied to clinical trials.
虽然利用造血干细胞进行基因治疗是该领域最早开展研究的方向,但尚未取得成功。然而,最近在更有效的基因转移和表达方法方面取得了重大进展。除了使用逆转录病毒载体取得了大幅改善的结果外,腺相关病毒载体和慢病毒载体在造血干细胞的稳定转导方面似乎也很有前景。这些在动物移植模型中得到证实的进展,目前正应用于临床试验。