1 Division of Internal Medicine, Department of Medicine, Allegheny General Hospital, Pittsburgh, PA. 2 Division of Nephrology and Hypertension, Department of Medicine, Allegheny General Hospital, Pittsburgh, PA.
Transplantation. 2017 Oct;101(10):2527-2535. doi: 10.1097/TP.0000000000001530.
Induction immunosuppression decreases the risk for acute rejection and improves graft outcomes in kidney transplant recipients (KTRs). We aimed to compare the outcomes of induction with Thymoglobulin and alemtuzumab in KTRs through paired-kidney analysis.
Using Organ Procurement and Transplantation Network/United Network for Organ Sharing database from 2003 to 2013, we identified recipients of deceased donor kidneys from the same donor in such a way that 1 patient received Thymoglobulin induction and recipient of the mate kidney underwent alemtuzumab induction. All patients were discharged on maintenance immunosuppression with tacrolimus and mycophenolate mofetil with/without steroids. Outcomes were compared between the groups in an adjusted model.
Study cohort included 1149 patients each in alemtuzumab and Thymoglobulin groups. Incidence of delayed graft function (25.8% vs 28.6%, P = 0.12), and 1-year rejection (5.7% vs 4.5%, P = 0.97) were similar for alemtuzumab versus Thymoglobulin groups. Adjusted overall graft (hazard ratio, 0.97; 95% confidence interval, 0.82-1.48; P = 0.52) and patient (hazard ratio, 0.86; 95% confidence interval, 0.69-1.05) survivals were also similar for alemtuzumab versus Thymoglobulin groups. Median hospital length of stay was significantly shorter in alemtuzumab group (4 days vs 5 days, P < 0.001). Similar findings were observed in a subgroup of high immune risk patients. There was evidence for clustering of alemtuzumab use within transplant centers which did not impact long-term outcomes.
Depleting antibody induction therapy with alemtuzumab and Thymoglobulin appear equally effective in deceased donor KTRs maintained on tacrolimus/mycophenolate mofetil-based regimen along with steroid. Alemtuzumab induction is beneficial in reducing hospital length of stay.
诱导免疫抑制可降低肾移植受者(KTR)发生急性排斥反应的风险,并改善移植物的预后。我们旨在通过配对肾脏分析比较 Thymoglobulin 和 alemtuzumab 在 KTR 中的诱导效果。
我们使用 2003 年至 2013 年期间的器官获取与移植网络/联合网络器官共享数据库,通过将来自同一供体的供体肾脏分配给一名患者接受 Thymoglobulin 诱导,而其配对肾脏接受 alemtuzumab 诱导,从而确定接受已故供体肾脏的患者。所有患者均在他克莫司和霉酚酸酯(伴有或不伴有类固醇)维持免疫抑制的情况下出院。在调整后的模型中比较了两组之间的结果。
研究队列包括 alemtuzumab 组和 Thymoglobulin 组各 1149 例患者。alemtuzumab 组和 Thymoglobulin 组的延迟移植物功能(25.8% vs. 28.6%,P=0.12)和 1 年排斥率(5.7% vs. 4.5%,P=0.97)相似。alemtuzumab 组和 Thymoglobulin 组的整体移植物(风险比,0.97;95%置信区间,0.82-1.48;P=0.52)和患者(风险比,0.86;95%置信区间,0.69-1.05)存活率也相似。alemtuzumab 组的中位住院时间明显更短(4 天 vs. 5 天,P<0.001)。在高免疫风险患者亚组中也观察到了类似的结果。alemtuzumab 的使用在移植中心内存在聚类现象,但并未影响长期结果。
在接受基于他克莫司/霉酚酸酯加类固醇的方案治疗的已故供体 KTR 中,用 alemtuzumab 和 Thymoglobulin 进行耗竭性抗体诱导治疗效果相当。alemtuzumab 诱导可降低住院时间。