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在尸体肾移植候选者中,应使用流式细胞术微球法而非抗人球蛋白法来检测HLA I类IgG抗体(PRA)。

Flow cytometry beads rather than the antihuman globulin method should be used to detect HLA Class I IgG antibody (PRA) in cadaveric renal regraft candidates.

作者信息

Bryan Christopher F, McDonald Scott B, Baier Karen A, Luger Alan M, Aeder Mark I, Murillo Daniel, Muruve Nicolas A, Nelson Paul W, Shield Charles F, Warady Bradley A

机构信息

Midwest Transplant Network, Westwood, KS 66205, USA.

出版信息

Clin Transplant. 2002;16 Suppl 7:15-23. doi: 10.1034/j.1399-0012.16.s7.2.x.

DOI:10.1034/j.1399-0012.16.s7.2.x
PMID:12372039
Abstract

HLA Class I antibody screening can be performed by flow cytometry using a mixture of 30 distinct bead populations each coated with the Class I antigen phenotype derived from different cell lines. In this study we compared the efficacy of Class I antibody screens done by flow cytometry beads with the antihuman globulin (AHG) method for patients awaiting cadaveric renal retransplantation. Class I panel reactive antibody (PRA) screening by flow cytometric beads of 21 regraft serum samples that had all been found to be negative by AHG DTT Class I PRA, revealed that 57.1% (12 of 21) had a flow Class I PRA of > or = 10%. Furthermore, when five regraft sera with an intermediate PRA were screened (mean AHG DTT PRA = 33.2 +/- 13%) the mean flow Class I PRA almost doubled (mean flow PRA = 72.4 +/- 10.2%) (p < 0.01). When active UNOS waiting list regraft candidates, after several months of screening the Class I PRA by flow beads, were divided into the three PRA categories based on their peak flow Class I PRA value (0-20%, 21-79% and > or = 80%), the incidence of a positive flow cross-match was 0%, 72% and 85% and the incidence of retransplantation was 60%, 22% and 10%, in each of these groups, respectively. These data provided our histocompatibility laboratory with the rationale to stop performing the AHG PRA and perform only the flow Class I PRA method for regraft candidates.

摘要

HLA I类抗体筛查可通过流式细胞术进行,使用30种不同的微珠群体混合物,每个微珠群体都包被有源自不同细胞系的I类抗原表型。在本研究中,我们比较了流式细胞术微珠法与抗人球蛋白(AHG)法对等待尸体肾再移植患者进行I类抗体筛查的效果。对21份再次移植血清样本进行流式细胞术微珠I类群体反应性抗体(PRA)筛查,这些样本经AHG DTT I类PRA检测均为阴性,结果显示57.1%(21份中的12份)的流式I类PRA≥10%。此外,对5份中等PRA的再次移植血清进行筛查(平均AHG DTT PRA = 33.2±13%)时,平均流式I类PRA几乎翻倍(平均流式PRA = 72.4±10.2%)(p<0.01)。当根据其峰值流式I类PRA值(0 - 20%、21 - 79%和≥80%)将活跃的器官共享联合网络(UNOS)等待名单上的再次移植候选者分为三个PRA类别时,这些组中流式交叉配型阳性的发生率分别为0%、72%和85%,再次移植的发生率分别为60%、22%和10%。这些数据为我们的组织相容性实验室提供了依据,即停止进行AHG PRA检测,仅对再次移植候选者采用流式I类PRA方法。

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