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

Transfusion
|April 19, 2011
PubMed

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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