Spencer D M
Baylor College of Medicine, Department of Immunology, One Baylor Plaza/M929, Houston, TX 77030, USA.
Curr Opin Mol Ther. 2000 Aug;2(4):433-40.
The graduation of gene therapy from unfulfilled dreams to conventional therapy for genetic and acquired disorders will require a mastery of multiple disparate components including gene delivery vectors, regulated tissue-specific gene expression, control of immunity and manipulation of cell viability. Improvements in suicide genes have opened up a whole new treatment modality for treating hyperproliferative disorders and for designing animal models for disease. Along with herpes simplex virus-1 thymidine kinase, a host of additional suicide genes have been developed. A critical comparison of these will follow along with progress in utilizing these reagents for therapeutic benefits.
基因疗法要从未能实现的梦想转变为用于治疗遗传性和后天性疾病的常规疗法,需要掌握多个不同的组成部分,包括基因传递载体、受调控的组织特异性基因表达、免疫控制以及细胞活力的操纵。自杀基因的改进为治疗过度增殖性疾病和设计疾病动物模型开辟了一种全新的治疗方式。除了单纯疱疹病毒1型胸苷激酶外,还开发了许多其他自杀基因。接下来将对这些基因进行关键比较,并介绍利用这些试剂实现治疗益处的进展情况。