Diem P
Abteilung für Endokrinologie und Diabetologie, Medizinische Universitätsklinik, Inselspital, Bern.
Ther Umsch. 1993 Feb;50(2):114-8.
Even if the pathogenesis of type-I (insulin-dependent) diabetes mellitus is still not clarified in every detail, there is general agreement that this form of diabetes is induced by autoimmune mechanisms leading to beta-cell destruction. Therefore, it should theoretically be feasible to suppress the mechanism leading to type-I diabetes with appropriate and early immunotherapy. The current clinical data clearly document that the rate and duration of remissions in patients with newly diagnosed type-I diabetes can be increased significantly using appropriate immunosuppressive regimens. However, before these therapies can become standard therapy of type-I diabetes, the following important clinical requirements have to be fulfilled: the toxicity (especially to kidneys and beta-cells) has to be reduced, the patients should be diagnosed and treated in 'pre-diabetic' states, more selective immunosuppressive regimens have to be available in order to reduce the occurrence of treatment-associated lymphomas and neoplasias. Since accurate detection of 'pre-diabetic' patients is difficult and presents an immense logistic problem, it may take a long time before large-scale immunosuppressive therapies of type-I diabetes are feasible.
即使I型(胰岛素依赖型)糖尿病的发病机制尚未完全阐明,但人们普遍认为这种糖尿病形式是由自身免疫机制导致β细胞破坏所引起的。因此,从理论上讲,通过适当的早期免疫疗法抑制导致I型糖尿病的机制应该是可行的。目前的临床数据清楚地表明,使用适当的免疫抑制方案可以显著提高新诊断的I型糖尿病患者的缓解率和缓解持续时间。然而,在这些疗法成为I型糖尿病的标准疗法之前,必须满足以下重要的临床要求:必须降低毒性(尤其是对肾脏和β细胞的毒性),患者应在“糖尿病前期”状态下被诊断和治疗,必须有更具选择性的免疫抑制方案以减少与治疗相关的淋巴瘤和肿瘤的发生。由于准确检测“糖尿病前期”患者很困难且存在巨大的后勤问题,I型糖尿病的大规模免疫抑制疗法可能需要很长时间才能实现。