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ABO 血型不相容的肾移植受者晚期抗体介导排斥反应的结局和风险分层:一项回顾性研究。

Outcomes and risk stratification for late antibody-mediated rejection in recipients of ABO-incompatible kidney transplants: a retrospective study.

机构信息

Transplant Institute, NYU Langone Medical Center, New York, NY, USA.

Department of Surgery, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Transpl Int. 2017 Sep;30(9):874-883. doi: 10.1111/tri.12969. Epub 2017 Jun 2.

Abstract

The required intensity of monitoring for antibody-mediated rejection (AMR) after of ABO-incompatible (ABOi) kidney transplantation is not clearly formulized. We retrospectively evaluated a single-center cohort of 115 ABO-incompatible (ABOi) kidney transplant recipients, of which 32% were also HLA incompatible (ABOi/HLAi) with their donors. We used an adjusted negative binomial model to evaluate risk factors for late AMR. Using this model, we risk-stratified patients into high- and low-risk groups for the development of late AMR; 26% of patients had at least one AMR episode; 49% of AMR episodes occurred within 30-days after transplant and were considered early AMR. Patients with an early AMR episode had a 5.5-fold greater incidence of developing late AMR [IRR = 5.5, (95% CI: 1.5-19.3), P = 0.01]. ABOi/HLAi recipients trended toward increased late AMR risk [IRR = 1.9, (95% CI: 0.5-6.6), P = 0.3]. High-risk recipients (those with an early AMR or those who were ABOi/HLAi) had a sixfold increased incidence of late AMR [IRR = 6.3, (95% CI: 1.6-24.6), P = 0.008] versus low-risk recipients. The overall incidence of late AMR was 20.8% vs. 1.5% in low-risk recipients. Changes in anti-A/B titer did not correlate with late AMR (IRR = 0.9 per log titer increase, P = 0.7). This risk-stratification scheme uses information available within 30 days of ABOi transplantation to determine risk for late AMR and can help direct longitudinal follow-up for individual patients.

摘要

抗 ABO 抗体介导排斥反应(AMR)监测的强度在 ABO 不相容(ABOi)肾移植后尚未明确规定。我们回顾性评估了 115 例 ABO 不相容(ABOi)肾移植受者的单中心队列,其中 32%的供者与受者 HLA 也不相容(ABOi/HLAi)。我们使用调整后的负二项式模型来评估晚期 AMR 的危险因素。使用该模型,我们将患者分为发生晚期 AMR 的高风险和低风险组;26%的患者至少发生过一次 AMR 发作;49%的 AMR 发作发生在移植后 30 天内,被认为是早期 AMR。发生早期 AMR 发作的患者发生晚期 AMR 的发生率增加了 5.5 倍[IRR=5.5,(95%CI:1.5-19.3),P=0.01]。ABOi/HLAi 受者发生晚期 AMR 的风险呈增加趋势[IRR=1.9,(95%CI:0.5-6.6),P=0.3]。高风险受者(发生早期 AMR 或 ABOi/HLAi)发生晚期 AMR 的发生率增加了六倍[IRR=6.3,(95%CI:1.6-24.6),P=0.008],与低风险受者相比。晚期 AMR 的总发生率为 20.8%,而低风险受者为 1.5%。抗-A/B 滴度的变化与晚期 AMR 无关(IRR=每对数滴度增加 0.9,P=0.7)。该风险分层方案利用 ABOi 移植后 30 天内获得的信息来确定晚期 AMR 的风险,并可帮助指导个体患者的纵向随访。

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