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储存血小板浓缩物中的趋化因子。

Chemokines in stored platelet concentrates.

作者信息

Bubel S, Wilhelm D, Entelmann M, Kirchner H, Klüter H

机构信息

Institute of Immunology and Transfusion Medicine, University of Lübeck School of Medicine, Lübeck, Germany.

出版信息

Transfusion. 1996 May;36(5):445-9. doi: 10.1046/j.1537-2995.1996.36596282589.x.

Abstract

BACKGROUND

Platelets contain several mediators, belonging to a family of proinflammatory cytokines named chemokines, that are stored in the organelles. Release and accumulation of these chemokines during storage of platelet concentrates (PCs) might be responsible for nonhemolytic transfusion reactions.

STUDY DESIGN AND METHODS

Analysis was done of pH and the levels of platelet factor 4, beta-thromboglobulin, interleukin 8, RANTES, macrophage-inflammatory protein-1 alpha, lactate dehydrogenase, and serotonin in the supernatant of stored PCs on Days 1, 3, 5, and 8. PCs were prepared by apheresis or from pools of four buffy coats. Buffy coat PCs were filtered before storage.

RESULTS

Nonfiltered apheresis PCs, which had a higher white cell contamination (p < 0.01), contained significantly more platelets than did buffy coat PCs (p = 0.02). The pH decreased significantly in apheresis PCs (p = 0.01), whereas there was a significant increase in lactate dehydrogenase (p < 0.001). In buffy coat PCs, pH remained stable and lactate dehydrogenase increased moderately. Concentrations of platelet factor 4 and beta-thromboglobulin increased steadily in both preparations over the storage period (p < 0.001). Macrophage-inflammatory protein-1 alpha was hardly detectable in the supernatant of both PCs, while RANTES levels increased significantly with storage time (p < 0.001). Interleukin 8 was not found in the supernatant of any PCs, with the exception of one apheresis PC with high white cell contamination (> 10(9)/ L). Serotonin levels were higher in apheresis PCs (p = 0.01), but the levels did not correlate with storage time.

CONCLUSION

Platelet factor 4, beta-thromboglobulin, and RANTES were released from platelets during storage and accumulated over time in the PCs. These chemokines might play a causative role in nonhemolytic transfusion reactions because of their inflammatory potential, but the clinical effects of the transfusion of PCs with high chemokine contents remain to be investigated.

摘要

背景

血小板含有多种介质,属于一类名为趋化因子的促炎细胞因子家族,这些介质存储在细胞器中。血小板浓缩物(PCs)储存期间这些趋化因子的释放和积累可能是导致非溶血性输血反应的原因。

研究设计与方法

对储存第1、3、5和8天的PCs上清液的pH值以及血小板因子4、β-血小板球蛋白、白细胞介素8、调节激活正常T细胞表达和分泌的趋化因子(RANTES)、巨噬细胞炎性蛋白-1α、乳酸脱氢酶和5-羟色胺水平进行分析。PCs通过单采或从四份白膜层混合制备。白膜层PCs在储存前进行过滤。

结果

白细胞污染较高(p < 0.01)的未过滤单采PCs所含血小板明显多于白膜层PCs(p = 0.02)。单采PCs的pH值显著下降(p = 0.01),而乳酸脱氢酶显著升高(p < 0.001)。在白膜层PCs中,pH值保持稳定,乳酸脱氢酶适度升高。在储存期间,两种制剂中血小板因子4和β-血小板球蛋白的浓度均稳步增加(p < 0.001)。两种PCs的上清液中几乎检测不到巨噬细胞炎性蛋白-1α,而RANTES水平随储存时间显著增加(p < 0.001)。除一份白细胞污染较高(> 10⁹/L)的单采PCs外,任何PCs的上清液中均未发现白细胞介素8。单采PCs中的5-羟色胺水平较高(p = 0.01),但该水平与储存时间无关。

结论

血小板因子4、β-血小板球蛋白和RANTES在储存期间从血小板中释放,并随时间在PCs中积累。由于这些趋化因子具有炎症潜能,它们可能在非溶血性输血反应中起致病作用,但输注趋化因子含量高的PCs的临床效果仍有待研究。

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