Abstract

ObjectiveThe 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.MethodsSingle 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.ResultsThere 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.ConclusionRising 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.

Highlights

  • The association of blood product transfusion with a variety of systemic reactions is well described

  • Rising concentrations of vascular endothelial growth factor (VEGF) occur during storage of single donor platelet concentrates due to platelet secretion or disintegration, but not due to leukocyte contamination

  • 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 transfusion-related acute lung injury (TRALI) associated with platelet products

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Summary

Introduction

The association of blood product transfusion with a variety of systemic reactions is well described. The most common of these reactions are the non-hemolytic transfusion reactions which occur most often with platelets, with units stored for longer periods, and appear to be related most often to soluble substances in the transfused plasma [1]. These disorders include a reaction characterized by non-cardiogenic pulmonary edema known as transfusion-related acute lung injury (TRALI) [2]. Contaminating leukocytes may be the predominant source of elevations in cytokines which have been linked to some transfusion reactions, but such elevations are detectable in only a minority of platelet units implicated in non-hemolytic transfusion reactions [6]. Platelets themselves likely contribute to these reactions as some 15-20% of platelets become activated during storage with subsequent degranulation and release of mediators such as soluble CD40 ligand

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