Screening plateletpheresis donors for HLA antibodies on two high-throughput platforms and correlation with recipient outcome.
Screening plateletpheresis donors for HLA antibodies on two high-throughput platforms and correlation with recipient outcome.
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DOI:
10.1111/j.1537-2995.2010.02874.x
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发表时间:
2011-03
期刊:
影响因子:
2.9
通讯作者:
Stroncek DF
中科院分区:
文献类型:
--
作者:
Quillen K;Medrano C;Adams S;Peterson B;Hackett J;Leitman SF;Klein HG;Stroncek DF
To determine the prevalence and impact of transfusing plasma containing leukocyte antibodies, we compared two high-throughput HLA antibody screening assays, and prospectively examined the medical records of all platelet recipients to detect subtle manifestations of TRALI and other transfusion reactions. Serum samples from 136 plateletpheresis donors were tested for HLA Class I and II antibodies using microbead (Labscreen PRA) and microchip (Dynachip) assays. Electronic medical records of all recipients were reviewed for vital signs and nursing documentation before and after transfusion. In the microchip assay with a cutoff value of 0.25, 2.9% of samples were positive for Class I, and 8.9% for Class II antibodies; with a cutoff value of 0.1, the results were 14.9% and 21.6% respectively. In the microbead assay (NBG ratio 1.5), 15% were positive for Class I, and 21% for Class II antibodies. The prevalence of HLA antibodies was 17% in donors without pregnancy or transfusion history, and 47% in donors with such history. The platelets were transfused in 265 episodes to 67 patients. There were no reported reactions; however, symptoms or vital sign changes were noted in 7 transfusion episodes. The incidence of reactions was 2.7% (2/75) for antibody-positive units and 2.6% (5/190) for antibody-negative units. Microbead and microchip assays yielded similar results. The prevalence of HLA antibodies was greater in donors with a history of pregnancy or transfusion, but no increase in the incidence of transfusion reactions was noted in recipients of components from donors with HLA antibodies.
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