Loi Michele M, Kelher Marguerite, Dzieciatkowska Monika, Hansen Kirk C, Banerjee Anirban, West F Bernadette, Stanley Crystal, Briel Matthew, Silliman Christopher C
Department of Research Laboratory, University of Colorado Denver, Aurora, Colorado.
Department of Pediatrics, University of Colorado Denver, Aurora, Colorado.
Transfusion. 2018 Aug;58(8):2003-2012. doi: 10.1111/trf.14788. Epub 2018 Sep 1.
Three methods of leukoreduction (LR) are used worldwide: filtration, buffy coat removal (BCR), and a combination of the previous two methods. Additionally, there are a number of additive solutions (ASs) used to preserve red blood cell (RBC) function throughout storage. During RBC storage, proinflammatory activity accumulates; thus, we hypothesize that both the method of LR and the AS affect the accumulation of proinflammatory activity.
Ten units of whole blood were drawn from healthy donors, the RBC units were isolated, divided in half by weight, and leukoreduced by: 1) BCR, 2) filtration, or 3) BCR and filtration (combination-LR); stored in bags containing AS-3 per AABB criteria; and sampled weekly. The supernatants were isolated and frozen (-80°C). RBC units drawn from healthy donors into AS-1-, AS-3-, or AS-5-containing bags were also stored and sampled weekly, and the supernatants were isolated and frozen. The supernatants were assayed for neutrophil (PMN)-priming activity and underwent proteomic analyses.
Filtration and combination LR decreased priming activity accumulation versus buffy coat LR, although the accumulation of priming activity was not different during storage. Combination LR increased hemolysis versus filtration via proteomic analysis. Priming activity from AS-3 units was significant later in storage versus AS-1- or AS-5-stored units.
Although both filtration and combination LR decrease the accumulation of proinflammatory activity versus buffy coat LR, combination LR is not more advantageous over filtration, has increased costs, and may cause increased hemolysis. In addition, AS-3 decreases the early accumulation of PMN-priming activity during storage versus AS-1 or AS-5.
全球范围内使用三种白细胞去除(LR)方法:过滤、去除白膜层(BCR)以及前两种方法的联合使用。此外,有多种添加剂溶液(ASs)用于在整个储存过程中保存红细胞(RBC)功能。在红细胞储存期间,促炎活性会累积;因此,我们假设白细胞去除方法和添加剂溶液都会影响促炎活性的累积。
从健康供体采集10单位全血,分离出红细胞单位,按重量均分为两半,并通过以下方式进行白细胞去除:1)BCR,2)过滤,或3)BCR与过滤(联合白细胞去除);按照美国血库协会(AABB)标准储存在含有AS-3的袋子中;每周取样。分离出上清液并冷冻(-80°C)。将从健康供体采集到含有AS-1、AS-3或AS-5的袋子中的红细胞单位也进行储存并每周取样,分离出上清液并冷冻。检测上清液中的中性粒细胞(PMN)启动活性并进行蛋白质组学分析。
与白膜层白细胞去除相比,过滤和联合白细胞去除降低了启动活性的累积,尽管在储存期间启动活性的累积没有差异。通过蛋白质组学分析,联合白细胞去除与过滤相比增加了溶血。与储存在AS-1或AS-5中的单位相比,AS-3单位的启动活性在储存后期更为显著。
尽管与白膜层白细胞去除相比,过滤和联合白细胞去除都降低了促炎活性的累积,但联合白细胞去除并不比过滤更具优势,成本更高,且可能导致溶血增加。此外,与AS-1或AS-5相比,AS-3在储存期间降低了PMN启动活性的早期累积。