在一项大型前瞻性横断面研究中,肾移植受者的晚期抗体介导的排斥反应——BORTEJECT试验筛选阶段的初步结果。

Clinical transplants Pub Date : 2014-01-01
Farsad Eskandary, Gregor Bond, Heinz Regele, Nicolas Kozakowski, Zeljko Kikić, Markus Wahrmann, Helmuth Haslacher, Rainer Oberbauer, Vido Ramassar, Philip Halloran, Georg A Böhmig
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引用次数: 0

摘要

在未选择的移植队列中,晚期抗体介导的排斥反应(ABMR)率的数据有限。在这里,我们调查了大量长期接受同种异体肾移植的患者中ABMR的患病率和特征。患者在随机对照试验(BORTEJECT研究;ClinicalTrials.gov: NCT01873157)旨在调查硼替佐米对晚期ABMR病程的影响。该研究(于2013年10月启动)包括横断面ABMR筛查(关键纳入标准:≥180天功能移植),以确定44名有资格纳入干预试验的受体。采用固相技术对患者进行供体特异性抗体(DSA)筛查,DSA+受体接受方案活检。截至2014年11月,已有714名受者完成了ABMR筛查(移植后中位数为6.5年)。101例患者(14%)的DSA高于1000平均荧光强度(MFI)的阈值。接受活检的78名DSA+受者中有44名(占总队列的6%)被诊断为c4d阳性(n = 17)或阴性(n = 27) ABMR, 40名同意参加干预试验。DSA+ABMR+和DSA+ABMR-患者在最高水平DSA的MFI方面存在显著差异(P < 0.001), MFI值可以中度预测ABMR或C4d阳性(受试者工作特征曲线下面积分别为0.75和0.84)。总之,本横断面分析结果表明晚期ABMR患病率≥6%。我们证明,循环DSA的更频繁发现可能不一定与ABMR诊断相关,特别是在抗体水平低的患者中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Late Antibody-Mediated Rejection in a Large Prospective Cross-Sectional Study of Kidney Allograft Recipients--Preliminary Results of the Screening Phase of the BORTEJECT Trial.

There is limited data on the rate of late antibody-mediated rejection (ABMR) in unselected transplant cohorts. Here, we investigated the prevalence and characteristics of ABMR in a large cohort of long-term kidney allograft recipients. Patients were screened in the context of a randomized controlled trial (BORTEJECT study; ClinicalTrials.gov: NCT01873157) designed to investigate the impact of bortezomib on the course of late ABMR. The study (initiation in October 2013) includes a cross-sectional ABMR screening (key inclusion criterion: functioning graft at ≥ 180 days) to identify 44 recipients eligible for inclusion in the intervention trial. Patients were screened for donor-specific antibodies (DSA) applying solid phase technology and DSA+ recipients underwent protocol biopsies. Through November 2014, ABMR screening (after a median of 6.5 years post-transplantation) had been completed for 714 recipients. One hundred one patients (14%) had DSA above a threshold of 1,000 mean fluorescence intensity (MFI). Forty-four of 78 DSA+ recipients (6% of the overall cohort) subjected to biopsy were diagnosed with C4d-positive (n = 17) or -negative (n = 27) ABMR and 40 consented to participate in the intervention trial. DSA+ABMR+ and DSA+ABMR- patients differed significantly with respect to the MFI of the highest level DSA (P < 0.001), whereby ABMR or C4d positivity were moderately predicted by MFI values (area under the receiver operating characteristic curve: 0.75 and 0.84, respectively). In conclusion, the results of this cross-sectional analysis suggest a ≥ 6% prevalence of late ABMR. We demonstrate that the more frequent finding of circulating DSA may not necessarily associate with ABMR diagnosis, especially in patients with low antibody levels.

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