Lacy P E
Department of Pathology, Washington University School of Medicine, St. Louis, MO 63110.
Mt Sinai J Med. 1994 Jan;61(1):23-31.
It is obvious that islet transplantation as an isograft can produce normoglycemia and can prevent and reverse early complications of diabetes in rodents. It is possible to produce normoglycemia in immunosuppressed diabetic patients with human islet transplants. It is possible to prevent rejection of islets in animals without continuous immunosuppression by immunoalteration of the islets, and this approach will be attempted in human diabetes. Finally, the encapsulation approach for prevention of rejection of islets is promising. Large animals will be used to test prototypes of the hollow fibers for humans, and if these experiments are successful, it will be possible to progress rapidly to human diabetes. The first approach with encapsulation in human diabetes would be to use human islets, then encapsulated pig islets, and finally genetically engineered beta cell lines when they become available. I hope that these approaches in islet transplantation will prevent the devastating diabetic complications that Henry Dolger demonstrated many years ago could occur in diabetic patients even though those patients are taking insulin.
显然,作为同种移植的胰岛移植能够使啮齿动物产生正常血糖水平,并能预防和逆转糖尿病的早期并发症。对于免疫抑制的糖尿病患者,用人胰岛移植有可能使其产生正常血糖水平。通过对胰岛进行免疫改造,有可能在不进行持续免疫抑制的情况下防止动物体内胰岛的排斥反应,这种方法将在人类糖尿病治疗中尝试。最后,用于预防胰岛排斥反应的封装方法很有前景。将使用大型动物来测试适用于人类的中空纤维原型,如果这些实验成功,将有可能迅速应用于人类糖尿病治疗。在人类糖尿病治疗中采用封装方法的第一步将是使用人胰岛,然后是封装的猪胰岛,最后在基因工程β细胞系可用时使用它们。我希望胰岛移植中的这些方法能够预防多年前亨利·多尔格所证明的即使糖尿病患者使用胰岛素也可能发生的毁灭性糖尿病并发症。