Department of Surgery, Yonsei University College of Medicine, Seoul, Republic of Korea.
Int Urol Nephrol. 2012 Oct;44(5):1549-57. doi: 10.1007/s11255-012-0169-1. Epub 2012 Apr 15.
The number of end-stage renal disease (ESRD) patients with preformed antibodies waiting for a kidney transplant has been increasing lately. We conducted a nationwide study on the outcomes of kidney transplantation after desensitization in Korea.
Six transplant centers have run desensitization programs. The patients who underwent living donor kidney transplantation after desensitization from 2002 to 2010 were retrospectively analyzed.
A total of 86 cases were enrolled. Thirty-five of these were cases of re-transplantation (40.7 %). Indications of desensitization were positive complement-dependent cytotoxicity (CDC) cross-match responses (CDC(+), 36.0 %), positive flow-cytometric cross-match responses (FCX(+), 54.7 %), and positive donor-specific antibodies (DSA(+), 8.1 %). The desensitization protocols used pre-transplant plasmapheresis (95.3 %), intravenous immunoglobulin (62.8 %), and rituximab (67.4 %). Acute rejection occurred in 18 patients (20.9 %), graft failure occurred in 4 patients, and the 3-year graft survival rate was 93.8 %. The presence of DSA increased the acute rejection rate (P = 0.015) and decreased the 1-year post-transplant estimated glomerular filtration rate (P = 0.006). Although rejection-free survival rates did not differ significantly between the CDC(+) and FCX(+) groups, the 1-year estimated glomerular filtration rate was lower in the CDC(+) group (P = 0.010). Infectious and significant bleeding complications occurred in 15.5 % and 4.7 % of cases, respectively.
Kidney transplantation after desensitization had good graft outcomes and tolerable complications in Korea, and therefore, this therapy can be recommended for sensitized ESRD patients.
近来,等待肾移植的终末期肾病(ESRD)患者中预存抗体的数量一直在增加。我们在韩国进行了一项关于脱敏后肾移植结局的全国性研究。
六家移植中心开展了脱敏项目。回顾性分析了 2002 年至 2010 年期间接受脱敏后活体供肾移植的患者。
共纳入 86 例患者,其中 35 例为再次移植(40.7%)。脱敏的适应证为补体依赖性细胞毒性(CDC)交叉配型反应阳性(CDC(+),36.0%)、流式细胞交叉配型反应阳性(FCX(+),54.7%)和供体特异性抗体阳性(DSA(+),8.1%)。使用的脱敏方案包括移植前血浆置换(95.3%)、静脉注射免疫球蛋白(62.8%)和利妥昔单抗(67.4%)。18 例(20.9%)患者发生急性排斥反应,4 例患者发生移植物失功,3 年移植物存活率为 93.8%。DSA 的存在增加了急性排斥反应的发生率(P=0.015),降低了移植后 1 年的估计肾小球滤过率(P=0.006)。尽管 CDC(+)和 FCX(+)组之间的无排斥反应存活率无显著差异,但 CDC(+)组的 1 年估计肾小球滤过率较低(P=0.010)。分别有 15.5%和 4.7%的患者发生感染和明显出血并发症。
韩国脱敏后肾移植具有良好的移植物结局和可耐受的并发症,因此,该疗法可推荐用于致敏的 ESRD 患者。