Schemmer Peter, Mehrabi Arianeb, Kraus Thomas, Sauer Peter, Gutt Carsten, Uhl Waldemar, Büchler Markus W
Department of General Surgery, Ruprecht-Karls-University, Im Neuenheimer Feld 110, 69120 Heidelberg, Germany.
Nephrol Dial Transplant. 2004 Jul;19 Suppl 4:iv26-35. doi: 10.1093/ndt/gfh1038.
The aetiology of primary graft non-function and dysfunction is unknown but most likely involves Kupffer cell-dependent reperfusion injury; however, reasons for transplant failure are complex and involve organ retrieval, preservation and transplantation. Important factors include the donor's condition, cold and warm ischaemic times, operative complications in the recipient, the immune status of the recipient and surgical experience. The donor operation and surgical technique also have an effect on outcome after transplantation. This is important, since surgical organ manipulation of the liver during harvest cannot be prevented completely with standard procedures. This is especially true during organ harvest for living-donor liver transplantation and split-liver transplantation in general. Most recently, an experimental setting has conclusively demonstrated that gentle in situ organ manipulation by touching, retracting and moving liver lobes gently during harvest dramatically reduces survival after transplantation via Kupffer cell-dependent mechanisms. These mechanisms involve disturbances of hepatic microcirculation, a hypermetabolic state of the liver, hypoxia and almost complete denudation of endothelial lining cells. Glycine, a non-essential, non-toxic amino acid, which prevents activation of Kupffer cells, prevented all effects of harvest-related injury to the liver when given before transplantation. Based on these data, intravenous glycine has been administered to patients before reperfusion of their liver transplant. Both serum transaminases and the rate of primary non-function have been dramatically reduced, compared with historic controls. These preliminary clinical results with glycine before reperfusion are promising for further improvement of the overall outcome after liver transplantation.
原发性移植肝功能无功能及功能障碍的病因尚不清楚,但很可能涉及库普弗细胞依赖性再灌注损伤;然而,移植失败的原因很复杂,涉及器官获取、保存和移植。重要因素包括供体状况、冷缺血和热缺血时间、受体的手术并发症、受体的免疫状态以及手术经验。供体手术和手术技术也会对移植后的结果产生影响。这很重要,因为在获取肝脏时,用标准程序无法完全避免对肝脏的手术操作。在活体供肝移植和一般劈离式肝移植的器官获取过程中尤其如此。最近,一个实验环境已确凿证明,在获取肝脏时通过轻轻触摸、牵拉和移动肝叶进行轻柔的原位器官操作,会通过库普弗细胞依赖性机制显著降低移植后的存活率。这些机制包括肝微循环紊乱、肝脏的高代谢状态、缺氧以及内皮衬里细胞几乎完全剥脱。甘氨酸是一种非必需、无毒的氨基酸,可防止库普弗细胞激活,在移植前给予时可预防与获取相关的肝脏损伤的所有影响。基于这些数据,在肝移植再灌注前已对患者静脉注射甘氨酸。与历史对照相比,血清转氨酶和原发性无功能的发生率均显著降低。这些再灌注前使用甘氨酸的初步临床结果有望进一步改善肝移植后的总体结果。