Klein Harvey G
Department of Transfusion Medicine, Clinical Center, National Institutes of Health, Bethesda, MD, United States of America.
Blood Transfus. 2017 Mar;15(2):107-111. doi: 10.2450/2017.0306-16.
The advent of preservative solutions permitted refrigerated storage of red blood cells. However, the convenience of having red blood cell inventories was accompanied by a disadvantage. Red cells undergo numerous physical and metabolic changes during cold storage, the "storage lesion(s)". Whereas controlled clinical trials have not confirmed the clinical importance of such changes, ethical and operational issues have prevented careful study of the oldest stored red blood cells. Suggestions of toxicity from meta-analyses motivated us to develop pre-clinical canine models to compare the freshest vs the oldest red blood cells. Our model of canine pneumonia with red blood cell transfusion indicated that the oldest red blood cells increased mortality, that the severity of pneumonia is important, but that the dose of transfused red blood cells is not. Washing the oldest red blood cells reduces mortality by removing senescent cells and remnants, whereas washing fresher cells increases mortality by damaging the red blood cell membrane. An opposite effect was found in a model of haemorrhagic shock with reperfusion injury. Physiological studies indicate that release of iron from old cells is a primary mechanism of toxicity during infection, whereas scavenging of cell-free haemoglobin may be beneficial during reperfusion injury. Intravenous iron appears to have toxicity equivalent to old red blood cells in the pneumonia model, suggesting that intravenous iron and old red blood cells should be administered with caution to infected patients.
保存液的出现使得红细胞能够冷藏保存。然而,拥有红细胞库存带来便利的同时也存在一个缺点。红细胞在冷藏储存期间会发生许多物理和代谢变化,即“储存损伤”。尽管对照临床试验尚未证实这些变化的临床重要性,但伦理和操作问题阻碍了对储存时间最长的红细胞进行仔细研究。荟萃分析中有关毒性的提示促使我们开发临床前犬类模型,以比较最新鲜和最陈旧的红细胞。我们的犬类输血性肺炎模型表明,最陈旧的红细胞会增加死亡率,肺炎的严重程度很重要,但输注红细胞的剂量并不重要。洗涤最陈旧的红细胞可通过去除衰老细胞和残余物来降低死亡率,而洗涤较新鲜的细胞则会因损伤红细胞膜而增加死亡率。在出血性休克伴再灌注损伤的模型中发现了相反的效果。生理学研究表明,衰老细胞中铁的释放是感染期间毒性的主要机制,而清除游离血红蛋白在再灌注损伤期间可能有益。在肺炎模型中,静脉注射铁似乎具有与陈旧红细胞相当的毒性,这表明静脉注射铁和陈旧红细胞在给感染患者使用时应谨慎。