The Critical Care Research Group, The Prince Charles Hospital, The University of Queensland, Brisbane, Qld, Australia.
Vox Sang. 2011 Nov;101(4):282-90. doi: 10.1111/j.1423-0410.2011.01511.x. Epub 2011 Sep 21.
BACKGROUND AND OBJECTIVES Severe transfusion-related acute lung injury (TRALI) events have been linked to donor-derived neutrophil antibodies. The journey to developing mass donor neutrophil antibody screening platforms is challenged by the fragility of neutrophils and their unique-specific antigenic characteristics. MATERIAL AND METHODS This article critically evaluates the capabilities and potential of five emerging antibody screening platforms designed to detect neutrophil reactive antibodies relevant to TRALI. They are compared with established neutrophil serological methods. RESULTS Data from two recombinant antigen platforms and a method using human neutrophil antigens-expressing KY cells indicated high specificity. Two mixed cellular flow cytometric assays have the advantage of presenting native conformation of the human polymorphonuclear neutrophil antigenic epitopes. CONCLUSIONS To date, the number and specificity of test sera applied to each platform is small. This needs to be substantially increased and further rigorous serological evaluation is yet needed to compare the sensitivity and specificity limits of each new platform with classical methods. With a limited world supply of TRALI-relevant test sera, a collaborative effort of laboratories with neutrophil and TRALI investigation expertise is required.
严重的输血相关急性肺损伤(TRALI)事件与供体来源的中性粒细胞抗体有关。由于中性粒细胞的脆弱性及其独特的特异性抗原特征,开发大规模供体中性粒细胞抗体筛选平台的道路充满挑战。
本文批判性地评估了五个新兴的抗体筛选平台的能力和潜力,这些平台旨在检测与 TRALI 相关的中性粒细胞反应性抗体。并与现有的中性粒细胞血清学方法进行了比较。
两种重组抗原平台和一种使用表达人类中性粒细胞抗原的 KY 细胞的方法的数据显示出高特异性。两种混合细胞流式细胞术检测法具有呈现人类多形核中性粒细胞抗原表位天然构象的优势。
迄今为止,每个平台应用的测试血清数量和特异性都很小。这需要大大增加,并进一步进行严格的血清学评估,以比较每个新平台与经典方法的灵敏度和特异性极限。由于 TRALI 相关测试血清的世界供应有限,因此需要具有中性粒细胞和 TRALI 研究专业知识的实验室进行合作。