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女性献血者中的白细胞反应性抗体:奥地利的经验

Leukocyte-Reactive Antibodies in Female Blood Donors: The Austrian Experience.

作者信息

Schönbacher Marlies, Aichinger Nicole, Weidner Lisa, Jungbauer Christof, Grabmer Christoph, Schuha Beate, Rohde Eva, Mayr Wolfgang, Körmöczi Günther

机构信息

Department of Blood Group Serology and Transfusion Medicine, Medical University of Vienna, Vienna, Austria.

Department of Transfusion Medicine, University Hospital Salzburg, Salzburg, Austria.

出版信息

Transfus Med Hemother. 2021 Mar;48(2):99-108. doi: 10.1159/000509946. Epub 2020 Sep 23.

Abstract

INTRODUCTION

Antibody-mediated transfusion-related acute lung injury (TRALI) is caused by antibodies against human leukocyte antigens (HLAs) or human neutrophil antigens (HNAs), and is one of the most serious complications associated with transfusion medicine. Prevention strategies like testing allo-exposed female blood donors have not yet been introduced nationwide in Austria. To assess the need and feasibility of routine leukocyte antibody testing, the prevalence of leukocyte-reactive antibodies in an Austrian female donor population was been determined using classical cell-based methods which were compared with a high-throughput bead-based method.

METHODS

Sera from 1,022 female blood donors were screened using a granulocyte aggregation test (GAT) and a white blood cell immunofluorescence test (WIFT) after retesting and specification of positive samples by granulocyte immunofluorescence test (GIFT) and monoclonal antibody-specific immobilization of granulocyte antigens (MAIGA). Potential HLA reactivities were confirmed using the microbeads assay LabScreen Mixed. The results in 142 donor sera and 38 well-defined reference sera were investigated by the microbeads assay LabScreen Multi and compared with classical cell-based methods.

RESULTS

Reactivity with either granulocytes and/or lymphocytes was detected in 79 sera (7.7%), with the majority being HLA-specific. Antibodies against HNA were obtained in 7 samples (0.7%). The aggregating potential of the detected antibodies was observed in 9 cases (0.9%). Most of the leukocyte-reactive antibodies occurred at a donor age of between 35 and 59 years ( = 61). LabScreen Multi showed good agreement (κ = 0.767) for HNA antibody detection by cell-based assays, but double/multiple specificities (100% of 7 anti-HNA-1b sera) as well as false-negative results (40% of 15 HNA-3-specific sera) occurred.

DISCUSSION

Leukocyte-reactive antibody screening is advised in Austrian female donors for safe blood transfusion, including single-donor convalescent plasma treatment of COVID-19 that may be implemented soon. For the introduction of LabScreen Multi, the combination with GAT should be considered to ensure correct anti-HNA-3a detection.

摘要

引言

抗体介导的输血相关急性肺损伤(TRALI)由针对人类白细胞抗原(HLA)或人类中性粒细胞抗原(HNA)的抗体引起,是输血医学中最严重的并发症之一。像检测曾接触过同种异体抗原的女性献血者这样的预防策略在奥地利尚未全国推行。为评估常规白细胞抗体检测的必要性和可行性,采用经典的基于细胞的方法测定了奥地利女性献血者群体中白细胞反应性抗体的流行率,并与高通量的基于微珠的方法进行了比较。

方法

对1022名女性献血者的血清进行粒细胞聚集试验(GAT)和白细胞免疫荧光试验(WIFT)筛查,之后通过粒细胞免疫荧光试验(GIFT)和粒细胞抗原单克隆抗体特异性固定法(MAIGA)对阳性样本进行复测和鉴定。使用微珠检测法LabScreen Mixed确认潜在的HLA反应性。通过微珠检测法LabScreen Multi研究了142份献血者血清和38份明确界定的参考血清的结果,并与经典的基于细胞的方法进行比较。

结果

在79份血清(7.7%)中检测到与粒细胞和/或淋巴细胞的反应性,其中大多数为HLA特异性。在7份样本(0.7%)中获得了针对HNA的抗体。在9例(0.9%)中观察到检测到的抗体的聚集潜能。大多数白细胞反应性抗体出现在35至59岁的献血者中(n = 61)。LabScreen Multi在基于细胞的检测中对HNA抗体检测显示出良好的一致性(κ = 0.767),但出现了双重/多重特异性(7份抗HNA - 1b血清中的100%)以及假阴性结果(15份HNA - 3特异性血清中的40%)。

讨论

为确保安全输血,建议对奥地利女性献血者进行白细胞反应性抗体筛查,包括可能很快实施的COVID - 19单供体恢复期血浆治疗。对于引入LabScreen Multi,应考虑将其与GAT结合以确保正确检测抗HNA - 3a。

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