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血小板输注改变血小板减少症患者的 CD40L 血液水平和释放能力。

Platelet transfusion alters CD40L blood level and release capacity in patients suffering from thrombocytopenia.

机构信息

Institute for Transplantation Diagnostics and Cell Therapeutics, Heinrich-Heine University Medical Center Düsseldorf, Düsseldorf, Germany.

出版信息

Transfusion. 2012 Jun;52(6):1213-20. doi: 10.1111/j.1537-2995.2011.03438.x. Epub 2011 Nov 14.

Abstract

BACKGROUND

Platelet (PLT)-derived cytokines, such as soluble CD40 ligand (sCD40L), play an important role in the development of adverse transfusion reactions associated with the administration of PLT products. In this study, we determined sCD40L concentration and release capacity in patients with thrombocytopenia before and after receiving a PLT transfusion.

STUDY DESIGN AND METHODS

The study included 12 patients suffering from chemotherapy-induced thrombocytopenia. sCD40L levels and release capacity were measured in plasma samples of the patients before and after PLT administration as well as in the respective plateletpheresis concentrates by enzyme-linked immunosorbent assay. Sixteen healthy blood donors served as a control group.

RESULTS

In PLT concentrates, elevated sCD40L levels (2567±134 pg/mL) were observed in comparison to plasma sCD40L levels in controls (238.4±35.3 pg/mL). sCD40L plasma concentration of patients with thrombocytopenia was significantly reduced (86.3±16.7 pg/mL) before transfusion and increased to nearly normal levels (204.4±24.8 pg/mL) after PLT administration. In parallel, the sCD40L release capacity per PLT showed no significant difference between controls and patients with thrombocytopenia before transfusion (33.3±2.6 and 29.3±4.6 ag/PLT, respectively) but was significantly reduced after PLT transfusion (22.4±2.7 compared to 29.3±4.6 ag/PLT).

CONCLUSIONS

In patients with thrombocytopenia, sCD40L levels were clearly influenced by PLT transfusions: PLT administration led to a normalization of sCD40L plasma concentration. Nevertheless, adverse transfusion reactions did not occur in these patients. The sCD40L release capacity was enhanced by PLT administration dependent on the increase in the amount of PLT count.

摘要

背景

血小板(PLT)衍生细胞因子,如可溶性 CD40 配体(sCD40L),在与 PLT 产品给药相关的不良输血反应的发展中起重要作用。在这项研究中,我们在接受 PLT 输血前后测定了患有血小板减少症的患者的 sCD40L 浓度和释放能力。

研究设计和方法

这项研究包括 12 名因化疗引起的血小板减少症患者。通过酶联免疫吸附试验测定患者 PLT 给药前后以及相应的血小板单采浓缩物中的 sCD40L 水平和释放能力。16 名健康献血者作为对照组。

结果

与对照组血浆 sCD40L 水平(238.4±35.3pg/mL)相比,PLT 浓缩物中 sCD40L 水平升高(2567±134pg/mL)。血小板减少症患者的 sCD40L 血浆浓度在输血前明显降低(86.3±16.7pg/mL),输血后接近正常水平(204.4±24.8pg/mL)。同时,PLT 输血前后,对照组和血小板减少症患者的 sCD40L 释放能力 per PLT 无显著差异(分别为 33.3±2.6 和 29.3±4.6ag/PLT),但 PLT 输血后明显降低(22.4±2.7 与 29.3±4.6ag/PLT 相比)。

结论

在血小板减少症患者中,sCD40L 水平明显受到 PLT 输血的影响:PLT 给药导致 sCD40L 血浆浓度正常化。然而,这些患者并未发生不良反应输血反应。PLT 给药依赖于 PLT 计数的增加而增强 sCD40L 的释放能力。

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