Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Más filtros




Base de datos
Intervalo de año de publicación
1.
Blood Adv ; 4(21): 5527-5539, 2020 11 10.
Artículo en Inglés | MEDLINE | ID: mdl-33166402

RESUMEN

Extracellular vesicles (EVs) are active components of red blood cell (RBC) concentrates and may be associated with beneficial and adverse effects of transfusion. Elucidating controllable factors associated with EV release in RBC products is thus important to better manage the quality and properties of RBC units. Erythrocyte-derived EVs (EEVs) and platelet-derived EVs (PEVs) were counted in 1226 RBC units (administered to 280 patients) using a standardized cytometry-based method. EV size and CD47 and annexin V expression were also measured. The effects of donor characteristics, processing methods, and storage duration on EV counts were analyzed by using standard comparison tests, and analysis of covariance was used to determine factors independently associated with EV counts. PEV as well as EEV counts were higher in whole-blood-filtered RBC units compared with RBC-filtered units; PEV counts were associated with filter type (higher with filters associated with higher residual platelets), and CD47 expression was higher on EEVs in RBC units stored longer. Multivariate analysis showed that EEV counts were strongly associated with filter type (P < .0001), preparation, and storage time (+25.4 EEV/µL per day [P = .01] and +42.4 EEV/µL per day [P < .0001], respectively). The only independent factor associated with PEV counts was the residual platelet count in the unit (+67.1 PEV/µL; P < .0001). Overall, processing methods have an impact on EV counts and characteristics, leading to large variations in EV quantities transfused into patients. RBC unit processing methods might be standardized to control the EV content of RBC units if any impacts on patient outcomes can be confirmed. The IMIB (Impact of Microparticles in Blood) study is ancillary to the French ABLE (Age of Transfused Blood in Critically Ill Adults) trial (ISRCTN44878718).


Asunto(s)
Conservación de la Sangre , Vesículas Extracelulares , Adulto , Transfusión Sanguínea , Enfermedad Crítica , Eritrocitos , Humanos
2.
Haematologica ; 101(3): e72-6, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26635040

Asunto(s)
Plaquetas/inmunología , Micropartículas Derivadas de Células/inmunología , Células Dendríticas/inmunología , Receptores X del Hígado/inmunología , Transportador 1 de Casete de Unión a ATP/genética , Transportador 1 de Casete de Unión a ATP/inmunología , Proteínas Angiogénicas/genética , Proteínas Angiogénicas/inmunología , Benzoatos/farmacología , Bencilaminas/farmacología , Plaquetas/citología , Plaquetas/efectos de los fármacos , Micropartículas Derivadas de Células/química , Células Dendríticas/citología , Células Dendríticas/efectos de los fármacos , Células Endoteliales/citología , Células Endoteliales/efectos de los fármacos , Células Endoteliales/inmunología , Regulación de la Expresión Génica , Humanos , Hidrocarburos Fluorados/farmacología , Hidroxicolesteroles/farmacología , Imidazoles/farmacología , Inmunidad Innata , Receptores X del Hígado/agonistas , Receptores X del Hígado/antagonistas & inhibidores , Receptores X del Hígado/genética , FN-kappa B/genética , FN-kappa B/inmunología , Oligodesoxirribonucleótidos/genética , Oligodesoxirribonucleótidos/inmunología , Fenilendiaminas/farmacología , Cultivo Primario de Células , Receptores Acoplados a Proteínas G , Transducción de Señal , Proteína 1 de Unión a los Elementos Reguladores de Esteroles/genética , Proteína 1 de Unión a los Elementos Reguladores de Esteroles/inmunología , Sulfonamidas/farmacología , Receptor Toll-Like 7/antagonistas & inhibidores , Receptor Toll-Like 7/genética , Receptor Toll-Like 7/inmunología , Factor de Necrosis Tumoral alfa/genética , Factor de Necrosis Tumoral alfa/inmunología
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA