Sun D S, Yagi T, Oyama T, Matsukawa H, Matsuda H, Sadamori H, Inagaki M, Matsuoka J, Iwagaki H, Tanaka N
Department of Gastroenterological Surgery and Transplant, Okayama University Graduate School of Medicine and Dentistry, Okayama, Japan.
J Int Med Res. 2003 Jul-Aug;31(4):281-9. doi: 10.1177/147323000303100405.
Donor-specific immunosuppression is important in transplant surgery. We examined the effect of intraportal donor-specific bone marrow transplantation on heterotopic small bowel transplantation in the high responder rat combination, ACI to Lewis. The study comprised five treatment groups: untreated controls (group 1); FK506 alone (group 2); low-dose predonine + FK506 (group 3); high-dose predonine + FK506 (group 4); and intraportal donor-specific bone marrow transplantation + FK506 (group 5). Intraportal transplantation was performed pre-operatively and FK506 and predonine given post-operatively. Intestinal allograft survival and changes of intragraft cytokine expression were analysed using the reverse transcription polymerase chain reaction. Allograft survival (mean +/- SD) was lowest in group 1 and greatest in group 5. The group 5 treatment regimen also down-regulated interferon-gamma and interleukin-2 transcription in the transplanted intestine. Intraportal donor bone marrow transplant combined with FK506 immunosuppression was found therefore to be the most beneficial treatment regimen.
供体特异性免疫抑制在移植手术中很重要。我们研究了门静脉内供体特异性骨髓移植对高反应性大鼠组合(从 ACI 到 Lewis)异位小肠移植的影响。该研究包括五个治疗组:未治疗的对照组(第 1 组);单独使用 FK506(第 2 组);低剂量泼尼松 + FK506(第 3 组);高剂量泼尼松 + FK506(第 4 组);门静脉内供体特异性骨髓移植 + FK506(第 5 组)。门静脉内移植在术前进行,FK506 和泼尼松在术后给予。使用逆转录聚合酶链反应分析肠道同种异体移植物的存活情况和移植物内细胞因子表达的变化。同种异体移植物存活率(平均值±标准差)在第 1 组中最低,在第 5 组中最高。第 5 组的治疗方案还下调了移植肠中干扰素-γ和白细胞介素-2 的转录。因此,发现门静脉内供体骨髓移植联合 FK506 免疫抑制是最有益的治疗方案。