Transplant Institute, NYU Langone Medical Center, New York, NY, USA.
Department of Surgery, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Transpl Int. 2017 Sep;30(9):874-883. doi: 10.1111/tri.12969. Epub 2017 Jun 2.
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.
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。