血小板血管内皮生长因子是输血相关急性肺损伤的潜在介质。

James P Maloney, Daniel R Ambruso, Norbert F Voelkel, Christopher C Silliman
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引用次数: 8

摘要

目的:非溶血性输血反应在血小板和血浆输注组发生率最高。其中一些反应的特征是内皮渗漏,特别是输血相关的急性肺损伤(TRALI)。在血液制品储存过程中,污染白细胞分泌的炎症介质浓度升高可能导致这种反应,但血小板分泌的介质也可能起作用。我们假设血小板储存导致内皮通透性介质血管内皮生长因子(VEGF)的积累,并且血管内给药外源性VEGF导致其与肺受体广泛结合。方法:单个供体,白细胞减少的单采血小板单位,保存5天以上。ELISA法测定离心上清中VEGF蛋白的含量,并定量白细胞污染对VEGF的潜在贡献。用离体灌注大鼠肺研究血管内给药放射性标记VEGF的摄取情况,以及未标记VEGF对肺渗漏的影响。结果:VEGF在血小板浓缩物血浆部分有时间依赖性释放(第1天为62±9 pg/ml,第5天为149±23 pg/ml;结论:单供血小板浓缩液储存过程中VEGF浓度升高是由于血小板分泌或崩解所致,而非白细胞污染所致。这些浓度的外源性VEGF迅速与肺血管中的受体结合。在较高的VEGF浓度下,VEGF在未受伤的肺中引起血管渗漏。这些数据提供了进一步的证据,VEGF可能有助于与血小板产物相关的TRALI中肺通透性增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Platelet Vascular Endothelial Growth Factor is a Potential Mediator of Transfusion-Related Acute Lung Injury.

Platelet Vascular Endothelial Growth Factor is a Potential Mediator of Transfusion-Related Acute Lung Injury.

Platelet Vascular Endothelial Growth Factor is a Potential Mediator of Transfusion-Related Acute Lung Injury.

Platelet Vascular Endothelial Growth Factor is a Potential Mediator of Transfusion-Related Acute Lung Injury.

Objective: The occurrence of non-hemolytic transfusion reactions is highest with platelet and plasma administration. Some of these reactions are characterized by endothelial leak, especially transfusion related acute lung injury (TRALI). Elevated concentrations of inflammatory mediators secreted by contaminating leukocytes during blood product storage may contribute to such reactions, but platelet-secreted mediators may also contribute. We hypothesized that platelet storage leads to accumulation of the endothelial permeability mediator vascular endothelial growth factor (VEGF), and that intravascular administration of exogenous VEGF leads to extensive binding to its lung receptors.

Methods: Single donor, leukocyte-reduced apheresis platelet units were sampled over 5 days of storage. VEGF protein content of the centrifuged supernatant was determined by ELISA, and the potential contribution of VEGF from contaminating leukocytes was quantified. Isolated-perfused rat lungs were used to study the uptake of radiolabeled VEGF administered intravascularly, and the effect of unlabeled VEGF on lung leak.

Results: There was a time-dependent release of VEGF into the plasma fraction of the platelet concentrates (62 ± 9 pg/ml on day one, 149 ± 23 pg/ml on day 5; mean ± SEM, p<0.01, n=8) and a contribution by contaminating leukocytes was excluded. Exogenous 125I-VEGF bound avidly and specifically to the lung vasculature, and unlabeled VEGF in the lung perfusate caused vascular leak.

Conclusion: Rising concentrations of VEGF occur during storage of single donor platelet concentrates due to platelet secretion or disintegration, but not due to leukocyte contamination. Exogenous VEGF at these concentrations rapidly binds to its receptors in the lung vessels. At higher VEGF concentrations, VEGF causes vascular leak in uninjured lungs. These data provide further evidence that VEGF may contribute to the increased lung permeability seen in TRALI associated with platelet products.

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