Stegall M D, Gloor J, Winters J L, Moore S B, Degoey S
Department of Surgery, Division of Transplantation Surgery, Mayo Clinic, Rochester, MN, USA.
Am J Transplant. 2006 Feb;6(2):346-51. doi: 10.1111/j.1600-6143.2005.01178.x.
Several protocols allow for the successful transplantation of sensitized renal allograft recipients, yet no one best method has emerged. The aim of the current study was to compare the efficacy of high-dose IVIG with two different plasmapheresis (PP)-based regimens in kidney transplant recipients with high levels of donor specific alloantibody (DSA) defined as a positive T-cell cytotoxicity crossmatch. With the primary goal of achieving a negative crossmatch, we employed three protocols sequentially between April 2000 and May 2005: (i) PP, low-dose IVIG, anti-CD20 antibody (n = 32); (ii) high-dose IVIG (n = 13); and (iii) PP, low-dose IVIG, anti-CD20 antibody and pre-transplant Thymoglobulin combined with post-transplant DSA monitoring (n = 16). IVIG decreased DSA activity in all treated patient, yet only 38% (5/13) achieved a negative crossmatch. In contrast, a negative crossmatch was achieved in 84% in PP group and 88% in the PP/monitoring group (p < 0.01 vs. IVIG). Even with a negative crossmatch, the rejection rates were 80% (IVIG), 37% (PP) and 29% (PP/monitoring), respectively, (p < 0.05 IVIG vs. PP). We conclude that multiple PP treatments leads to more reproducible desensitization and lower humoral rejection rates than a single high-dose of IVIG, but that no regimen was completely effective in preventing humoral rejection.
有几种方案可使致敏肾移植受者成功移植,但尚未出现一种最佳方法。本研究的目的是比较高剂量静脉注射免疫球蛋白(IVIG)与两种不同的基于血浆置换(PP)的方案在供体特异性同种异体抗体(DSA)水平高(定义为T细胞细胞毒性交叉配型阳性)的肾移植受者中的疗效。以实现交叉配型阴性为主要目标,我们在2000年4月至2005年5月期间依次采用了三种方案:(i)血浆置换、低剂量IVIG、抗CD20抗体(n = 32);(ii)高剂量IVIG(n = 13);(iii)血浆置换、低剂量IVIG、抗CD20抗体以及移植前使用胸腺球蛋白并结合移植后DSA监测(n = 16)。IVIG降低了所有治疗患者的DSA活性,但只有38%(5/13)的患者实现了交叉配型阴性。相比之下,血浆置换组84%的患者和血浆置换/监测组88%的患者实现了交叉配型阴性(与IVIG组相比,p < 0.01)。即使交叉配型为阴性,排斥反应发生率分别为80%(IVIG组)、37%(血浆置换组)和29%(血浆置换/监测组)(IVIG组与血浆置换组相比,p < 0.05)。我们得出结论,与单次高剂量IVIG相比,多次血浆置换治疗导致脱敏效果更可重复且体液排斥反应发生率更低,但没有一种方案能完全有效预防体液排斥反应。