Johnsson C, Tufveson G
Department of Transplantation Surgery, University Hospital, Uppsala, Sweden.
Transpl Int. 1994;7(6):392-7. doi: 10.1007/BF00346032.
The vitamin D analogue MC 1288 (20-epi-1 alpha,25-dihydroxycholecalciferol) was tested here for its possible immunosuppressive properties in vivo using different rat transplantation models. MC 1288, in a dose of 0.1 microgram/kg daily, administered intraperitoneally for 10 days, was found to be effective in prolonging cardiac allograft survival. Untreated recipients rejected their grafts around day 8 while MC 1288 treatment delayed rejection until day 22 (P < 0.001). Addition of the immunostimulatory drug LS-2616 (Linomide) reduced the immunosuppressive effect of MC 1288 and rejection occurred around day 11. The immunosuppressive effect of MC 1288 on rejection following small bowel transplantation was determined by measuring the amounts of hyaluronan (HA) secreted into the intestinal lumen. On day 6 post-transplantation the amounts of intraluminal HA in untreated animals was 29.2 +/- 5.3 ng/min and cm, while in MC 1288-treated animals it was just 5.0 +/- 1.6 ng/min and cm (P < 0.01). We conclude that MC 1288 has immunosuppressive effects that may make it suitable for the prevention of graft rejection.
在此,我们使用不同的大鼠移植模型,对维生素D类似物MC 1288(20-表-1α,25-二羟基胆钙化醇)在体内可能具有的免疫抑制特性进行了测试。发现以每日0.1微克/千克的剂量腹腔注射MC 1288,持续10天,可有效延长心脏同种异体移植物的存活时间。未治疗的受体在第8天左右排斥移植物,而MC 1288治疗可将排斥反应延迟至第22天(P<0.001)。添加免疫刺激药物LS-2616(利诺米德)可降低MC 1288的免疫抑制作用,排斥反应在第11天左右发生。通过测量分泌到肠腔内的透明质酸(HA)量,确定了MC 1288对小肠移植后排斥反应的免疫抑制作用。移植后第6天,未治疗动物肠腔内HA量为29.2±5.3纳克/分钟·厘米,而MC 1288治疗的动物仅为5.0±1.6纳克/分钟·厘米(P<0.01)。我们得出结论,MC 1288具有免疫抑制作用,这可能使其适用于预防移植物排斥反应。