van der Meer Pieter F, Bontekoe Ido J, Daal Brunette B, de Korte Dirk
Department of Product and Process Development, Sanquin Blood Bank, Amsterdam, the Netherlands.
Transfusion. 2015 Aug;55(8):1900-8. doi: 10.1111/trf.13033. Epub 2015 Mar 9.
Pathogen reduction technologies (PRTs) increase the safety of the blood supply, but are also associated with cell damage. Our aim was to investigate the effect of Mirasol PRT on platelet (PLT) concentrates stored in plasma and whether the use of a PLT additive solution (PAS) is able to improve in vitro quality.
Twenty-two buffy coats (BCs) were pooled and split into two equal parts. To one half, 2 units of plasma were added, and to the other, 2 units of SSP+ PAS were added. Each part was equally split in half again (to resemble pooling five BCs) and PLT concentrates were prepared. One plasma PLT concentrate was Mirasol treated, and the other served as control; similarly, one SSP+ PLT concentrate was Mirasol treated, and the other not. PLT concentrates were stored for 8 days (n = 12).
Mirasol PRT led to elevated lactate production in PLT concentrates in plasma, giving lower pH values throughout storage. The use of SSP+ mostly abrogated this effect, and Mirasol-treated PLT concentrates in SSP+ had only slightly higher lactate production rates and annexin A5 binding as control PLT concentrates in plasma. However, irrespective whether plasma or SSP+ was used, Mirasol PRT led to higher CD62P expression and lower hypotonic shock response (HSR) scores.
Mirasol treatment leads to higher PLT activation and lower HSR scores both when stored in plasma or SSP+. However, if Mirasol-treated PLTs are stored in SSP+, lactate metabolism and annexin A5 binding are lower, showing that PAS can partly mitigate the effect of PRT. The clinical relevance of this finding needs to be demonstrated.
病原体灭活技术(PRTs)可提高血液供应的安全性,但也会导致细胞损伤。我们的目的是研究Mirasol PRT对储存在血浆中的血小板(PLT)浓缩物的影响,以及使用血小板添加剂溶液(PAS)是否能够改善体外质量。
将22份 Buffy 层(BCs)混合并分成两等份。其中一份加入2单位血浆,另一份加入2单位SSP+PAS。每一份再均分为两半(类似于混合5份BCs)并制备PLT浓缩物。一份血浆PLT浓缩物接受Mirasol处理,另一份作为对照;同样,一份SSP+PLT浓缩物接受Mirasol处理,另一份不处理。PLT浓缩物储存8天(n = 12)。
Mirasol PRT导致血浆中PLT浓缩物的乳酸生成增加,在整个储存过程中pH值降低。使用SSP+大多消除了这种影响,并且在SSP+中经Mirasol处理的PLT浓缩物的乳酸生成率和膜联蛋白A5结合仅略高于血浆中的对照PLT浓缩物。然而,无论使用血浆还是SSP+,Mirasol PRT都会导致更高的CD62P表达和更低的低渗休克反应(HSR)评分。
无论储存在血浆还是SSP+中,Mirasol处理都会导致更高的PLT活化和更低 的HSR评分。然而,如果经Mirasol处理的PLT储存在SSP+中,乳酸代谢和膜联蛋白A5结合会更低,表明PAS可以部分减轻PRT的影响。这一发现的临床相关性需要得到证实。