Division of Nephrology, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Transplantation. 2012 Mar 15;93(5):493-502. doi: 10.1097/TP.0b013e3182427fc3.
We aimed to investigate the impact of antibody induction on outcomes in human leukocyte antigen (HLA) 0-mismatched deceased donor kidney recipients.
Using the Organ Procurement and Transplant Network/United Network of Organ Sharing database as of November 2009, we identified 44,008 adult deceased donor kidney recipients who received primary kidney transplants alone between 2003 and 2008 (HLA 0 mismatch, n = 6274; ≥ 1 mismatch, n=37,734; median follow-up: 834 days). The impact of induction (thymoglobulin, interleukin-2 receptor antagonists [IL-2RA], or alemtuzumab; vs. no induction) on rejection (initial hospitalization, 6 months, first year), death-censored graft failure, and mortality were analyzed using multivariate logistic and Cox regression in the two groups. The impact of individual agents on outcomes was further analyzed in 0-mismatch recipients.
There was a decreased risk of rejection over the first 6 months for HLA 0-mismatch recipients of antibody induction (adjusted odds ratio=0.71, P=0.003), but this effect was not observed at 1 year; in comparison, induction was associated with a reduced risk of rejection over the first year for HLA-mismatched recipients (0.87, P<0.001). The use of thymoglobulin (0.72, P=0.02) and IL-2RA (0.67, P=0.004) was associated with a decreased risk of rejection compared with no-induction at 6 months but was not different at 1 year (thymoglobulin: 0.77, P=0.05; IL-2RA:0.81, P=0.11) in HLA 0-mismatched recipients. Induction was not associated with improved graft or patient survival in HLA 0-mismatch recipients.
In HLA 0-mismatch deceased donor recipients, antibody induction was associated with a decreased risk of rejection at 6 months posttransplant. Its use did not improve graft and patient survival over the follow-up period.
本研究旨在探讨抗体诱导治疗对人类白细胞抗原(HLA)0 错配的尸体供肾受者结局的影响。
利用截至 2009 年 11 月的器官获取与移植网络/联合器官共享网络数据库,我们共纳入 2003 年至 2008 年间接受单纯尸体供肾移植的 44008 例成年受者(HLA 0 错配,n=6274;≥1 错配,n=37734;中位随访时间:834 天)。采用多变量逻辑回归和 Cox 回归分析诱导治疗(胸腺球蛋白、白细胞介素-2 受体拮抗剂[IL-2RA]或阿仑单抗;vs. 无诱导治疗)对两组受者移植后 6 个月内(初始住院期间、6 个月、第 1 年)排斥反应(排斥反应发生率、死亡相关移植物丢失和死亡率)的影响。进一步分析 0 错配受者中不同抗体诱导药物对结局的影响。
HLA 0 错配受者接受抗体诱导治疗后 6 个月内排斥反应风险降低(校正比值比=0.71,P=0.003),但该作用在第 1 年未观察到;相比之下,HLA 错配受者接受诱导治疗后第 1 年排斥反应风险降低(0.87,P<0.001)。与无诱导治疗相比,HLA 0 错配受者在第 6 个月时使用胸腺球蛋白(0.72,P=0.02)和 IL-2RA(0.67,P=0.004)可降低排斥反应风险,但在第 1 年时无差异(胸腺球蛋白:0.77,P=0.05;IL-2RA:0.81,P=0.11)。HLA 0 错配受者中,诱导治疗与移植物和患者存活率的改善无关。
在 HLA 0 错配的尸体供肾受者中,移植后 6 个月时使用抗体诱导治疗可降低排斥反应风险。但在随访期间,诱导治疗并未改善移植物和患者的存活率。