Transfusion Medicine Service, Australian Red Cross Blood Service, Adelaide, SA, Australia.
Br J Haematol. 2013 Aug;162(3):409-12. doi: 10.1111/bjh.12369. Epub 2013 May 8.
There are no accepted methods to predict the development of platelet transfusion refractoriness (PTR) due to human leucocyte antigen (HLA)-alloimmunization. Hence, matched platelets are usually given only to patients demonstrating PTR, necessarily resulting in some ineffective random donor platelets (RDPLT) transfusions. To assess its utility in predicting PTR, we retrospectively tested samples from 387 patients receiving chemotherapy for acute leukaemia or autologous transplantation using a micro-bead flow cytometry assay. The average of the mean fluorescence intensities (avgMFI) of the class I beads in the screening assay was correlated with outcomes of RDPLT transfusions during a 2 week period. Antibodies were detected in 57 patients; 66 developed PTR, of whom 28 were alloimmunized. avgMFI usefully predicted the development of PTR (area under the receiver operating curve 0.87, 95% confidence interval: 0.77-0.96). A logistic regression model estimated the probability of PTR to be >90% when avgMFI >5440. These results indicate that micro-bead flow cytometry assays could inform a risk-adapted strategy for managing thrombocytopaenic HLA allo-immunized patients.
由于人类白细胞抗原(HLA)同种免疫,目前尚无预测血小板输注难治性(PTR)发展的公认方法。因此,通常仅向表现出 PTR 的患者提供匹配的血小板,这必然导致一些无效的随机供体血小板(RDPLT)输注。为了评估其在预测 PTR 中的效用,我们使用微珠流式细胞术检测了 387 名接受急性白血病化疗或自体移植的患者的样本。在筛选检测中,I 类珠的平均荧光强度(avgMFI)与 2 周内 RDPLT 输注的结果相关。在 57 名患者中检测到抗体;66 名患者发生 PTR,其中 28 名患者发生同种免疫。avgMFI 可有效预测 PTR 的发展(受试者工作特征曲线下面积为 0.87,95%置信区间:0.77-0.96)。逻辑回归模型估计当 avgMFI >5440 时,PTR 的概率>90%。这些结果表明,微珠流式细胞术检测可提供一种风险适应策略,用于管理血小板减少性 HLA 同种免疫患者。