Herzog R W, High K A
The Children's Hospital of Philadelphia, Abramsom Research Center, PA 19104, USA.
Curr Opin Hematol. 1998 Sep;5(5):321-6. doi: 10.1097/00062752-199809000-00003.
The aim of gene therapy for hemophilia is the stable introduction and expression of a gene encoding functional blood coagulation factor VIII or IX. Although there are as yet no published studies demonstrating long-term expression of therapeutic levels in large animal models of the disease, there have been several reports over the past year of sustained expression of therapeutic levels of clotting factors in small animals, and some of these strategies are currently being applied to hemophilic dogs. Recent advances include optimized retroviral gene transfer, improved adenoviral vectors for high levels of sustained expression of factor VIII in mice, stable therapeutic levels of factor IX expression in mice after transduction of muscle or liver with adenoassociated virus vector, as well as new nonviral gene delivery strategies. Finally, several important mouse and dog models of hemophilia have been characterized during the past year.
血友病基因治疗的目标是稳定导入并表达编码功能性血液凝固因子VIII或IX的基因。尽管目前尚无已发表的研究表明在该疾病的大型动物模型中能实现治疗水平的长期表达,但在过去一年里有几篇报道称在小型动物中实现了凝血因子治疗水平的持续表达,并且其中一些策略目前正在应用于血友病犬。近期进展包括优化的逆转录病毒基因转移、用于在小鼠中高水平持续表达因子VIII的改良腺病毒载体、用腺相关病毒载体转导肌肉或肝脏后在小鼠中实现因子IX的稳定治疗水平表达,以及新的非病毒基因递送策略。最后,在过去一年里已经对几种重要的血友病小鼠和犬模型进行了特征描述。