储存对捐献红细胞中氧化生物标志物积累的影响。

L. Rael, R. Bar-Or, D. Ambruso, C. Mains, D. Slone, M. Craun, D. Bar-Or
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引用次数: 32

摘要

背景:输血相关性急性肺损伤(TRALI)是一种以氧化应激为特征的危及生命的疾病。填充红细胞(PRBC)和其他血液制品的储存时间较长与输血患者发生TRALI的风险增加有关。方法采用柠檬酸盐-磷酸盐-葡萄糖缓冲液4℃保存的含PRBC血液共10个单位。在Bonfils血液中心(Denver, CO),在第1天和第42天采集样本。样品立即离心,收集上清液并保存在-80℃,以待进一步分析。在第1天和第42天的样品中测量氧化还原电位和蛋白质氧化。结果第42天样品的氧化还原电位(98.1 mV +/- 21.9 SD)较第1天样品(62.6 mV +/- 21.5 SD)显著升高(p < 0.05)。人血清白蛋白的氧化率在贮藏期间提高了63.6%。其他血清蛋白如载脂蛋白A1和转甲状腺素也表现出类似的氧化增加。此外,观察到具有裂解的c端氨基酸的蛋白质表明存在羧基肽酶活性,这是炎症的标志。结论输血PRBC中氧化环境的存在随着保存时间的延长而增加。这可以部分解释与输入旧血液制品相关的TRALI风险增加的原因。
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The effect of storage on the accumulation of oxidative biomarkers in donated packed red blood cells.
BACKGROUND Transfusion-related acute lung injury (TRALI) is a life-threatening condition characterized by oxidative stress. Longer storage times of packed red blood cells (PRBC) and other blood products have been implicated with an increased risk in developing TRALI in transfused patients. METHODS A total of 10 units of blood containing PRBC stored in citrate-phosphate-dextrose buffer at 4 degrees C were included in the study. At Bonfils Blood Center (Denver, CO), samples were collected on storage day 1 and day 42. Samples were immediately centrifuged, and the supernatants were collected and stored at -80 degrees C until further analysis. Oxidation-reduction potential and protein oxidation were measured in both the day 1 and day 42 samples. RESULTS Oxidation-reduction potential significantly increased (p < 0.05) in the day 42 sample (98.1 mV +/- 21.9 SD) versus the day 1 sample (62.6 mV +/- 21.5 SD). The oxidation of human serum albumin increased by 63.6% during the storage time. Other serum proteins such as apolipoprotein A1 and transthyretin demonstrated similar increases in oxidation. Also, proteins with a cleaved C-terminal amino acid were observed indicating the presence of carboxypeptidase activity, a marker of inflammation. CONCLUSIONS The presence of an oxidative environment in transfused PRBC increases with storage time. This could partially explain the increased risk of developing TRALI related to the transfusion of older blood products.
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