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检测技术对肾移植等待名单中患者致敏状态的影响。

Influence of test technique on sensitization status of patients on the kidney transplant waiting list.

机构信息

Department of Transplantation Immunology, University of Heidelberg, Heidelberg, Germany.

出版信息

Am J Transplant. 2013 Aug;13(8):2075-82. doi: 10.1111/ajt.12332. Epub 2013 Jul 10.

DOI:10.1111/ajt.12332
PMID:23841891
Abstract

The exquisitely sensitive single antigen bead (SAB) technique was shown to detect human leukocyte antigen (HLA) antibodies in sera of healthy male blood donors. Such false reactions can have an impact on critical decisions, especially with respect to the determination of unacceptable HLA-antigen mismatches in patients awaiting a kidney transplant. We tested pretransplant sera of 534 patients on the kidney waiting list using complement-dependent cytotoxicity (CDC), enzyme-linked immunosorbent assay (ELISA) and SAB in parallel. Evidence of HLA antibodies was obtained in 5% of patients using CDC, 14% using ELISA, and 81% using SAB. Among patients without history of an immunizing event, 77% showed evidence of HLA antibodies in SAB. In contrast 98% of these patients were negative in ELISA and CDC. In patients without an immunizing event, SAB-detected antibodies reacted not always weakly but with mean fluorescence intensity (MFI) values as high as 14 440. High-MFI-value antibodies were found in some of these patients with HLA specificities that are rather common in general population, consideration of which would lead to unjustified exclusion of potential kidney donors. False SAB reactions can be unveiled by testing with additional antibody assays. Denial of donor kidneys to recipients based on HLA-antibody specificities detected exclusively in the SAB assay is not advisable.

摘要

灵敏的单抗原珠(SAB)技术被证明可以检测健康男性献血者血清中的人类白细胞抗原(HLA)抗体。这种假反应可能会对关键决策产生影响,特别是在确定等待肾移植的患者不可接受的 HLA 抗原不匹配时。我们使用补体依赖性细胞毒性(CDC)、酶联免疫吸附试验(ELISA)和 SAB 平行检测了 534 名等待肾移植患者的移植前血清。使用 CDC 在 5%的患者中获得了 HLA 抗体的证据,在 14%的患者中使用 ELISA,在 81%的患者中使用 SAB。在没有免疫事件史的患者中,77%的患者在 SAB 中显示出 HLA 抗体的证据。相比之下,这些患者中的 98%在 ELISA 和 CDC 中均为阴性。在没有免疫事件的患者中,SAB 检测到的抗体反应并不总是很弱,但平均荧光强度(MFI)值高达 14440。在这些患者中,一些具有 HLA 特异性的患者中存在高 MFI 值抗体,这些特异性在一般人群中相当常见,如果考虑到这一点,将导致对潜在肾供体的不合理排斥。通过额外的抗体检测可以揭示假 SAB 反应。仅在 SAB 检测中检测到 HLA 抗体而拒绝将供体肾脏提供给受者是不可取的。

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