Miyagawa J, Yamamoto K, Hanafusa T, Itoh N, Nakagawa C, Otsuka A, Katsura H, Yamagata K, Miyazaki A, Kono N
Second Department of Internal Medicine, Osaka University Medical School, Japan.
Diabetologia. 1990 Aug;33(8):503-5. doi: 10.1007/BF00405113.
We investigated the effect of an immunosuppressant FK-506 on histological change of islets, the onset of diabetes, and the change of spleen cell subsets in female non-obese diabetic mice. Mice administered intraperitoneally with FK-506 from 5 to 20 weeks of age showed marked suppression of mononuclear cell infiltration (insulitis) at 10 weeks of age. Among the subsets of the spleen cells, a significant decrease in the population of Thyl.2-positive T cells (pan-T), L3T4-positive T cells (mainly helper/inducer), and Lyt2-positive T cells (mainly suppressor/cytotoxic) was observed in FK-506-treated mice. Furthermore, glucose tolerance of the mice at 15 weeks of age was clearly improved. Cumulative incidence observed up to 40 weeks of age was 86% in control mice and 23% in FK-506-treated mice (p less than 0.01). These data indicate that FK-506 has a preventive effect on insulitis and diabetes by the suppression of cell-mediated autoimmunity in non-obese diabetic mice.
我们研究了免疫抑制剂FK - 506对雌性非肥胖型糖尿病小鼠胰岛组织学变化、糖尿病发病以及脾细胞亚群变化的影响。在5至20周龄时腹腔注射FK - 506的小鼠在10周龄时显示出单核细胞浸润(胰岛炎)受到显著抑制。在脾细胞亚群中,FK - 506处理的小鼠中Thyl.2阳性T细胞(全T细胞)、L3T4阳性T细胞(主要是辅助/诱导性T细胞)和Lyt2阳性T细胞(主要是抑制/细胞毒性T细胞)的数量显著减少。此外,15周龄小鼠的糖耐量明显改善。在40周龄时观察到的累积发病率在对照小鼠中为86%,在FK - 506处理的小鼠中为23%(p小于0.01)。这些数据表明,FK - 506通过抑制非肥胖型糖尿病小鼠的细胞介导自身免疫,对胰岛炎和糖尿病具有预防作用。