Cognasse Fabrice, Hamzeh-Cognasse Hind, Lafarge Sandrine, Acquart Sophie, Chavarin Patricia, Courbil Rémi, Fabrigli Patrick, Garraud Olivier
EFS Auvergne-Loire and Faculté de Médecine, GIMAP-EA3064, Université de Saint-Etienne, Saint-Etienne, France.
Transfusion. 2009 Jan;49(1):91-8. doi: 10.1111/j.1537-2995.2008.01931.x. Epub 2008 Oct 2.
Recent studies have demonstrated that infused platelets (PLTs) can promote inflammation. The objective of this study was to evaluate the impact of storage of transfusion-grade PLTs on the peripheral blood mononuclear cells (PBMNCs) of the recipient.
An in vitro cell model system was established to measure the degree of activation of donor PLTs during 5 days of their storage and then to measure immune cell activation by detecting marker expression in coculture experiments.
The level of soluble CD62p increased significantly by Day 3, and membrane expression of CD62p increased significantly from Day 2, indicating some degree of PLT activation over time during storage (p < 0.05). Donor PLTs and PBMNC subsets (monocytes, B cells, and T cells) from recipients were cocultured for 48 hours. The number of PLT-PBMNC subset doublets detected by flow cytometry was correlated with the PLT storage time after Day 3 (p < 0.05), indicating consistent binding of PLTs to PBMNCs. The results of these experiments showed that there was a consistent and significant increase in expression of conventional activation markers of T cells, B cells, and monocytes compared with appropriate controls (p < 0.05 to <0.01).
The results of this study indicate that, from Day 3 onward, activation markers are consistently expressed on PLTs. From these results, we conclude that activated PLTs may affect PBMNC interactions in recipients.
近期研究表明,输注的血小板(PLT)可促进炎症反应。本研究的目的是评估输血级血小板储存对受者外周血单个核细胞(PBMNC)的影响。
建立体外细胞模型系统,以测量供体血小板在储存5天期间的活化程度,然后通过在共培养实验中检测标志物表达来测量免疫细胞活化情况。
可溶性CD62p水平在第3天显著升高,CD62p的膜表达从第2天开始显著增加,表明储存期间血小板随时间推移有一定程度的活化(p < 0.05)。将供体血小板与受者的PBMNC亚群(单核细胞、B细胞和T细胞)共培养48小时。流式细胞术检测到的血小板 - PBMNC亚群双联体数量与第3天后的血小板储存时间相关(p < 0.05),表明血小板与PBMNC持续结合。这些实验结果表明,与适当对照相比,T细胞、B细胞和单核细胞的传统活化标志物表达持续且显著增加(p < 0.05至<0.01)。
本研究结果表明,从第3天起,血小板上持续表达活化标志物。根据这些结果,我们得出结论,活化的血小板可能会影响受者体内PBMNC的相互作用。