Suppr超能文献

供体血小板储存至少3天可引发受者血液单核细胞的活化标志物表达:一项体外研究。

Donor platelets stored for at least 3 days can elicit activation marker expression by the recipient's blood mononuclear cells: an in vitro study.

作者信息

Cognasse Fabrice, Hamzeh-Cognasse Hind, Lafarge Sandrine, Acquart Sophie, Chavarin Patricia, Courbil Rémi, Fabrigli Patrick, Garraud Olivier

机构信息

EFS Auvergne-Loire and Faculté de Médecine, GIMAP-EA3064, Université de Saint-Etienne, Saint-Etienne, France.

出版信息

Transfusion. 2009 Jan;49(1):91-8. doi: 10.1111/j.1537-2995.2008.01931.x. Epub 2008 Oct 2.

Abstract

BACKGROUND

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.

STUDY DESIGN AND METHODS

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.

RESULTS

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).

CONCLUSION

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.

摘要

背景

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。

研究设计与方法

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。

结果

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)。

结论

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验