External quality assessment of flow cytometric HLA-B27 typing.

Cytometry Pub Date : 2000-04-15
W H Levering, R van den Beemd, J G te Marvelde, W A van Beers, H Hooijkaas, K Sintnicolaas, J W Gratama
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Abstract

A biannual external quality assurance (EQA) scheme for flow cytometric typing of the HLA-B27 antigen is operational in The Netherlands and Belgium since 1995. We report here on the results of the first seven send-outs to which 36 to 47 laboratories participated. With the send-out, four specimens from blood bank donors, who had been typed for HLA Class I antigens by complement-dependent cytotoxicity, were distributed. Subtyping of the HLA-B27 allele was performed by PCR-SSP. Ten samples were HLA-B27(pos) (all HLA-B*2705) and 18 were HLA-B27(neg). For flow cytometry, the most widely monoclonal antibody (MoAb) used was FD705, followed by GS145.2 and ABC-m3. The majority of laboratories used more than 1 anti-HLA-B27 MoAb for typing. The HLA-B27(pos) samples were correctly classified as positive by the large majority of participants (median 95%; range 85% to 100% per send out); some participants considered further typing necessary and misclassification as negative was only sporadically seen. The classification of HLA-B27(neg) samples as negative was less straightforward. Ten samples were correctly classified as such by 97% (82% to 100%) of the participants, whereas 64% (range 53% to 70%) of the participants classified the remaining eight samples as HLA-B27(neg). There was no significant prevalence of a particular HLA-B allele among these eight "poor concordancy" samples as compared to the ten "good concordancy" samples. Inspection of the reactivity patterns of the individual MoAb with HLA-B27(neg) samples revealed that ABC-m3 showed very little cross-reactivity apart from its well-known cross-reactivity with HLA-B7, whereas the cross-reactivity patterns of GS145.2 and FD705 were more extensive. The small sample size (n = 18) and the distribution of HLA-B alleles other than HLA-B27 did not allow assignment of specificities to these cross-reactions. Finally, we showed that standardized interpretation of the combined results of two anti-HLA-B27 MoAb reduced the frequency of false-positive conclusions on HLA-B27(neg) samples. In this series, the lowest frequency of false-positive assignments was observed with the combination of the FD705 and ABC-m3 MoAb.

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流式细胞术HLA-B27分型的外部质量评价。
自1995年以来,荷兰和比利时开始实施一年两次的HLA-B27抗原流式细胞分型外部质量保证(EQA)计划。我们在此报告36至47个实验室参加的前7次派出的结果。在送出的同时,还分发了四份来自血库献血者的标本,这些献血者通过补体依赖性细胞毒性进行了HLA I类抗原的分型。采用PCR-SSP对HLA-B27等位基因进行分型。10例为HLA-B27(阳性)(均为HLA-B*2705), 18例为HLA-B27(阴性)。流式细胞术中使用最多的单克隆抗体(MoAb)是FD705,其次是GS145.2和ABC-m3。大多数实验室使用1种以上的抗hla - b27 MoAb进行分型。大多数参与者正确地将HLA-B27(pos)样本分类为阳性(中位数95%;每次发送的范围为85%至100%);一些参与者认为进一步的分类是必要的,错误分类为阴性只是偶尔看到。将HLA-B27(阴性)样本分类为阴性则不那么直接。97%(82%至100%)的参与者将10个样本正确分类,而64%(53%至70%)的参与者将其余8个样本分类为HLA-B27(阴性)。与10个“良好一致性”样本相比,这8个“差一致性”样本中没有明显的特定HLA-B等位基因的流行。对单个MoAb与HLA-B27(阴性)样品的反应模式的检验表明,ABC-m3除了与HLA-B7具有众所周知的交叉反应性外,几乎没有交叉反应,而GS145.2和FD705的交叉反应模式更为广泛。小样本量(n = 18)和HLA-B等位基因除HLA-B27外的分布不允许对这些交叉反应分配特异性。最后,我们发现对两种抗HLA-B27 MoAb联合结果的标准化解释减少了HLA-B27(阴性)样品假阳性结论的频率。在该系列中,FD705和ABC-m3 MoAb组合的假阳性鉴定频率最低。
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