Kolodka T M, Finegold M, Moss L, Woo S L
Howard Hughes Medical Institute, Baylor College of Medicine, Houston, TX 77030, USA.
Proc Natl Acad Sci U S A. 1995 Apr 11;92(8):3293-7. doi: 10.1073/pnas.92.8.3293.
Type 1 diabetes mellitus is caused by severe insulin deficiency secondary to the autoimmune destruction of pancreatic beta cells. Patients need to be controlled by periodic insulin injections to prevent the development of ketoacidosis, which can be fatal. Sustained, low-level expression of the rat insulin 1 gene from the liver of severely diabetic rats was achieved by in vivo administration of a recombinant retroviral vector. Ketoacidosis was prevented and the treated animals exhibited normoglycemia during a 24-hr fast, with no evidence of hypoglycemia. Histopathological examination of the liver in the treated animals showed no apparent abnormalities. Thus, the liver is an excellent target organ for ectopic expression of the insulin gene as a potential treatment modality for type 1 diabetes mellitus by gene therapy.
1型糖尿病是由胰腺β细胞自身免疫性破坏继发的严重胰岛素缺乏所致。患者需要通过定期注射胰岛素来控制病情,以预防可能致命的酮症酸中毒的发生。通过体内给予重组逆转录病毒载体,实现了严重糖尿病大鼠肝脏中大鼠胰岛素1基因的持续低水平表达。预防了酮症酸中毒,治疗后的动物在24小时禁食期间血糖正常,且无低血糖迹象。对治疗后动物的肝脏进行组织病理学检查未发现明显异常。因此,肝脏是胰岛素基因异位表达的理想靶器官,可作为基因治疗1型糖尿病的一种潜在治疗方式。