Tydén Gunnar, Donauer Johannes, Wadström Jonas, Kumlien Gunilla, Wilpert Jochen, Nilsson Thomas, Genberg Helena, Pisarski Przemislaw, Tufveson Gunnar
Departments of Transplantation Surgery and Transfusion Medicine, Karolinska University Hospital, Stockholm, Sweden.
Transplantation. 2007 May 15;83(9):1153-5. doi: 10.1097/01.tp.0000262570.18117.55.
A new protocol for ABO-incompatible kidney transplantation has recently been introduced. We report here on the joint experience of the implementation in Stockholm and Uppsala, Sweden and Freiburg, Germany.
The new protocol utilizes antigen-specific immunoadsorption to remove existing ABO-antibodies, rituximab, and intravenous immunoglobulin to prevent the rebound of antibodies, and conventional tacrolimus, mycophenolate-mofetil, and prednisolone immunosuppression. Sixty consecutive ABO-incompatible kidney transplantations were included in the study. The outcome is compared with the results of 274 ABO-compatible live donor transplantations performed during the same period.
Two of the ABO-incompatible grafts have been lost (non-compliance and death with functioning graft). All the remaining 58 grafts had good renal function at a follow-up of up to 61 months. We did not observe any late rebound of antibodies and there were no humoral rejections. Graft survival was 97% for the ABO-incompatible compared with 95% for the ABO-compatible. Patient survival was 98% in both groups. There was a significant variation in preoperative A/B-antibody titer between the centers, with a median 1:8 in Uppsala, median 1:32 in Stockholm and median 1:128 in Freiburg. More preoperative antibody adsorptions were therefore needed in Freiburg than in Stockholm and Uppsala.
The new protocol was easily implemented and there were no graft losses that could be related to ABO-incompatibility. A significant inter-institutional variation in the measurement of anti-AB-antibodies was found, having a substantial impact on the number of immunoadsorptions and consequently on the total cost for the procedure. A standardized fluorescence-activated cell sorting technique for antibody quantification is much needed.
最近引入了一种新的ABO血型不相容肾移植方案。我们在此报告瑞典斯德哥尔摩和乌普萨拉以及德国弗莱堡联合实施该方案的经验。
新方案利用抗原特异性免疫吸附去除现有的ABO抗体,使用利妥昔单抗和静脉注射免疫球蛋白预防抗体反弹,并采用传统的他克莫司、霉酚酸酯和泼尼松龙进行免疫抑制。该研究纳入了连续60例ABO血型不相容肾移植病例。将结果与同期进行的274例ABO血型相容活体供肾移植的结果进行比较。
2例ABO血型不相容移植肾失功(1例患者不依从,1例移植肾功能良好时死亡)。其余58例移植肾在长达61个月的随访中肾功能良好。我们未观察到抗体的任何晚期反弹,也未发生体液排斥反应。ABO血型不相容移植肾的存活率为97%,ABO血型相容移植肾的存活率为95%。两组患者的存活率均为98%。各中心术前A/B抗体滴度存在显著差异,乌普萨拉的中位数为1:8,斯德哥尔摩的中位数为1:32,弗莱堡的中位数为1:128。因此,弗莱堡比斯德哥尔摩和乌普萨拉需要更多的术前抗体吸附。
新方案易于实施,未出现与ABO血型不相容相关的移植肾失功情况。发现抗AB抗体检测存在显著的机构间差异,这对免疫吸附次数有重大影响,进而对该手术的总成本产生重大影响。非常需要一种标准化的荧光激活细胞分选技术来定量抗体。