C1q供体特异性抗体与高敏感肾移植受者移植后活检结果相关。

Clinical transplants Pub Date : 2016-01-01
Sarat Kuppachi, Danniele Holanda, Sara Gallegos, Elizabeth H Field
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引用次数: 0

摘要

供体特异性抗人白细胞抗原抗体(DSA)与肾移植中抗体介导的排斥反应(AMR)有关,但DSA患者的移植物损伤范围从无损伤到丰富的排斥反应。由于具有细胞毒性潜能的免疫球蛋白G (IgG)抗体可以通过其结合补体分数C1q来区分,因此C1q结合IgG (C1q+) DSA的水平可能对分层风险或诊断AMR有用。因此,我们研究了IgG和C1q+ DSA在预测肾活检AMR病理特征中的价值。我们对2014年12月后移植的连续高敏感患者进行了1、3和6个月的肾活检,并监测IgG和C1q+ DSA,测试了不同截止水平的DSA与活检中AMR病理特征之间的关系。8例cPRA >90%且血流交叉配型阴性的患者接受了肾移植,并完成了6个月的随访,提供23对活检/血清样本用于分析。C1q+ DSA在平均荧光强度(MFI)临界值>100 (p=0.046)和>300 (p=0.008)时与活检中C4d的发现显著相关,与常规IgG DSA相比,C1q+ DSA表现出更好的阳性和阴性预测值。C1q+ DSA对活检的任何AMR特征也显示出显著的相关性和良好的预测价值(p=0.003, >100 MFI;>300 MFI p=0.005), IgG DSA无相关性。在一小群高cPRA移植受者中,作为AMR活检结果的指标,C1q+ DSA优于IgG DSA。在移植后高度敏感患者的DSA监测中纳入C1q+ DSA检测有助于AMR的及时诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
C1q Donor-Specific Antibody Associates with Post-transplant Biopsy Findings in Highly- Sensitized Kidney Transplant Recipients.

Donor-specific anti-human leukocyte antigen antibodies (DSA) are associated with antibody-mediated rejection (AMR) in kidney transplantation, but the spectrum of graft injury seen in patients with DSA ranges from no damage to florid rejection. Since immunoglobulin G (IgG) antibodies with cytotoxic potential can be distinguished by their binding complement fraction C1q, the level of C1q-binding IgG (C1q+) DSA may be useful for stratifying risk or diagnosing AMR. We therefore investigated the value of IgG and C1q+ DSA in predicting pathologic features of AMR on kidney biopsies. We tested the associations between DSA at different cut-off levels and pathologic features of AMR on biopsy in a cohort of consecutive, highly-sensitized patients transplanted after December 2014 who had 1-, 3-, and 6-month protocol kidney biopsies and monitoring for IgG and C1q+ DSA. Eight patients with cPRA >90% and negative flow crossmatch underwent kidney transplant and completed six months of follow-up contributing 23 pairs of biopsy/ serum samples for analysis. C1q+ DSA was significantly associated with C4d finding on biopsy at mean fluorescence intensity (MFI) cut-offs of >100 (p=0.046) and >300 (p=0.008) and showed superior positive and negative predictive value in comparison to conventional IgG DSA. C1q+ DSA also showed significant association and good predictive value for any AMR feature on biopsy (p=0.003, for >100 MFI; p=0.005 for >300 MFI), while IgG DSA showed no association. In a small cohort of high cPRA transplant recipients, C1q+ DSA outperformed IgG DSA as an indicator of AMR biopsy findings. Including C1q+ DSA testing in post-transplant DSA monitoring of highly-sensitized patients may aid the timely diagnosis of AMR.

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