供体特异性IgM抗体在HLA不相容肾移植中的临床相关性:一项回顾性单中心研究。

Clinical transplants Pub Date : 2016-01-01
Adarsh Babu, Avgi Andreou, David Briggs, Nithya Krishnan, Rob Higgins, Dan Mitchell, Tom Barber, Sunil Daga
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引用次数: 0

摘要

针对供体人类白细胞抗原(HLA)的免疫球蛋白G (IgG)抗体在移植前和移植后被监测,因为它们在预测排斥反应和同种异体肾移植存活方面起着既定的作用。然而,免疫球蛋白M (IgM)抗hla供体特异性抗体(DSA)的作用尚不完全清楚,特别是在接受直接移植的高度敏感患者中。我们设计这项研究是为了确定IgM DSA是否能预测排斥事件和/或移植物衰竭。92例hla抗体不相容移植患者的样本在5个时间点进行检测:第8天(血浆置换前)、第0天、第7天、第14天和第30天,使用Luminex微珠试验,含乙二胺四乙酸洗涤缓冲液(LABScreen®,One Lambda, Canoga Park, CA)。如果平均荧光值大于2000,则IgM为阳性。移植前和移植后IgM的存在与早期抗体介导的排斥反应(移植后30天内)和移植失败相关。采用SPSS IBM软件进行统计分析。移植存活的估计是经过死亡审查的。移植前IgM DSA的存在不能预测排斥反应(p=0.83)或移植失败(p=0.424)。移植后IgM DSA水平在第14天达到峰值(与IgG DSA水平相似)。移植后(新生和再合成)IgM DSA的存在与排斥反应无关(p=0.83)。然而,移植后IgM与移植失败相关(p=0.037)。这项研究表明,移植后IgM DSA高于IgG的额外检测是重要的,因为移植后IgM DSA与移植失败有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Relevance of Donor-Specific IgM Antibodies in HLA Incompatible Renal Transplantation: A Retrospective Single-Center Study.

Immunoglobulin G (IgG) antibodies against donor human leukocyte antigens (HLA) are monitored in the pre-and post-transplant period due to their established role in predicting rejection and renal allograft survival. However, the role of immunoglobulin M (IgM) anti-HLA donor-specific antibodies (DSA) is not fully understood, especially in highly-sensitized patients undergoing direct transplantation. We designed this study to determine whether IgM DSA predicts rejection episodes and/or graft failure. Samples from 92 patients who had undergone HLA-antibody incompatible transplants were tested at 5 time points: days -8 (pre-plasmapheresis), 0, 7, 14, and 30 using Luminex microbead assay with ethylenediaminetetraacetic acid containing wash buffer (LABScreen®, One Lambda, Canoga Park, CA). IgM was defined positive if the mean fluorescence values were greater than 2000. Presence of pre- and post-transplant IgM was correlated with early antibody mediated rejection episodes (within 30 days post-transplantation) and graft failure. Statistical analyses were performed using SPSS IBM software. Graft survival estimates were death-censored. The presence of pre-transplant IgM DSA did not predict rejection (p=0.83) or graft failure (p=0.424). The post-transplant IgM DSA levels peaked at day 14 (similar to IgG DSA levels). Presence of IgM DSA post-transplant (de novo and resynthesis) was not associated with rejection (p=0.83). However, post-transplant IgM was associated with graft failure (p=0.037). This study shows additional testing of post-transplant IgM DSA over and above IgG is important as post-transplant IgM DSA is associated with graft failure.

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