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Routine Screening Method for Microparticles in Platelet Transfusions
Published on: January 31, 2018
Microparticles in stored red blood cells as potential mediators of transfusion complications
Wenche Jy1, Marco Ricci, Sherry Shariatmadar
1Wallace H. Coulter Platelet Laboratory, Division of Hematology and Oncology, Department of Medicine, University of Miami School of Medicine, Miami, Florida 33176, USA. wjy@med.miami.edu
Abstract:
This article reviews evidence for the involvement of cell-derived microparticles (MPs) in transfusion-related adverse events. The controversy concerning possible added risk of older versus fresher stored blood is also reviewed and is consistent with the hypothesis that MPs are involved with adverse events. Although all types of circulating MPs are discussed, the emphasis is on red blood cell-derived MPs (RMPs). The evidence is particularly strong for involvement of RMPs in transfusion-related acute lung injury, but also for postoperative thrombosis. However, this evidence is largely circumstantial. Work in progress to directly test the hypothesis is also briefly reviewed.
Insights
Cell-derived microparticles (MPs) may contribute to adverse events following blood transfusions. Evidence suggests red blood cell-derived MPs (RMPs) are linked to lung injury and thrombosis, though further research is needed.
Area of Science:
- Transfusion Medicine
- Hematology
- Immunology
Background:
- Cell-derived microparticles (MPs) are circulating fragments released from various cell types.
- MPs are implicated in various physiological and pathological processes, including thrombosis and inflammation.
- The role of MPs in blood transfusion complications remains an area of active investigation.
Purpose of the Study:
- To review the evidence linking cell-derived microparticles (MPs) to transfusion-related adverse events.
- To examine the hypothesis that storage duration of blood products influences the risk of adverse events via MPs.
- To focus on red blood cell-derived MPs (RMPs) and their potential contribution to specific complications.
Main Methods:
- Literature review of existing studies on microparticles and transfusion reactions.
- Analysis of evidence supporting the involvement of MPs in transfusion-related acute lung injury (TRALI) and postoperative thrombosis.
- Discussion of ongoing research aimed at directly testing the MP hypothesis.
Main Results:
- Circulating MPs, particularly red blood cell-derived MPs (RMPs), are reviewed for their potential role in adverse transfusion events.
- Evidence suggests a correlation between MPs and transfusion-related acute lung injury (TRALI) and postoperative thrombosis.
- The hypothesis that older stored blood may pose an increased risk due to MPs is consistent with current data, though evidence is largely circumstantial.
Conclusions:
- Cell-derived microparticles, especially RMPs, are potentially involved in transfusion-related adverse events.
- Further direct research is required to confirm the causal role of MPs in complications like TRALI and thrombosis.
- Understanding the MP contribution could inform strategies for safer blood transfusion practices.
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