Impact of production methods and storage conditions on extracellular vesicles in packed red blood cells and platelet concentrates

Transfus Apher Sci. 2024 Apr;63(2):103891. doi: 10.1016/j.transci.2024.103891. Epub 2024 Feb 5.

Abstract

The use of blood and blood products can be life-saving, but there are also certain risks associated with their administration and use. Packed red blood cells (pRBCs) and platelet concentrates are the most commonly used blood products in transfusion medicine to treat anemia or acute and chronic bleeding disorders, respectively. During the production and storage of blood products, red blood cells and platelets release extracellular vesicles (EVs) as a result of the storage lesion, which may affect product quality. EVs are subcellular structures enclosed by a lipid bilayer and originate from the endosomal system or from the plasma membrane. They play a pivotal role in intercellular communication and are emerging as important regulators of inflammation and coagulation. Their cargo and their functional characteristics depend on the cell type from which they originate, as well as on their microenvironment, influencing their capacity to promote coagulation and inflammatory responses. Hence, the potential involvement of EVs in transfusion-related adverse events is increasingly recognized and studied. Here, we review the knowledge regarding the effect of production and storage conditions of pRBCs and platelet concentrates on the release of EVs. In this context, the mode of processing and anticoagulation, the influence of additive solutions and leukoreduction, as well as the storage duration will be addressed, and we discuss potential implications of EVs for the clinical outcome of transfusion.

Keywords: Blood products; Extracellular vesicles; Packed red blood cells; Platelet concentrate; Storage lesion.

Publication types

  • Review

MeSH terms

  • Anemia*
  • Blood Platelets
  • Blood Preservation / methods
  • Blood Transfusion
  • Erythrocytes / metabolism
  • Extracellular Vesicles* / metabolism
  • Humans