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Microparticles in sickle cell anaemia: promise and pitfalls
Author(s) -
Hebbel Robert P.,
Key Nigel S.
Publication year - 2016
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/bjh.14112
Subject(s) - disease , cell , immunology , sickle cell anemia , medicine , biology , pathology , genetics
Summary Blood from patients with sickle cell disease contains microparticles ( MP ) derived from multiple cell sources, including red cells, platelets, monocytes and endothelial cells. MP s are of great interest because of their disease associations, their status as promising biomarkers, and the intercellular communications they mediate. To illustrate the likelihood of their relevance in sickle cell disease, we discuss the nature of MP , their profiling in sickle disease, some caveats relevant to their detection, their roles in supporting coagulation and the disparate influences they may exert upon the pathobiology of sickle cell disease.