Current Understanding of the Relationship between Blood Donor Variability and Blood Component Quality

被引:17
作者
Hadjesfandiari, Narges [1 ,2 ]
Khorshidfar, Mona [2 ]
Devine, Dana V. [1 ,2 ]
机构
[1] Canadian Blood Serv Ctr Innovat, Vancouver, BC V6T 1Z3, Canada
[2] Univ British Columbia, Ctr Blood Res, Vancouver, BC V6T 1Z3, Canada
关键词
blood transfusion; blood product quality; blood donor variability; platelet transfusion; red blood cell transfusion; SICKLE-CELL TRAIT; PLATELET-FUNCTION; SEX-DIFFERENCES; RED-CELLS; CLINICAL-OUTCOMES; STORAGE DURATION; BETA-THALASSEMIA; GLYCOPROTEIN-VI; OXYGEN-AFFINITY; TRANSFUSION;
D O I
10.3390/ijms22083943
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
While differences among donors has long challenged meeting quality standards for the production of blood components for transfusion, only recently has the molecular basis for many of these differences become understood. This review article will examine our current understanding of the molecular differences that impact the quality of red blood cells (RBC), platelets, and plasma components. Factors affecting RBC quality include cytoskeletal elements and membrane proteins associated with the oxidative response as well as known enzyme polymorphisms and hemoglobin variants. Donor age and health status may also be important. Platelet quality is impacted by variables that are less well understood, but that include platelet storage sensitive metabolic parameters, responsiveness to agonists accumulating in storage containers and factors affecting the maintenance of pH. An increased understanding of these variables can be used to improve the quality of blood components for transfusion by using donor management algorithms based on a donors individual molecular and genetic profile.
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页数:29
相关论文
共 150 条
[1]  
Albanyan A., 2015, J HLTH SPE C, V3, P53, DOI [10.4103/1658-600X.156104, DOI 10.4103/1658-600X.156104]
[2]   Assessment of leucoreduction of sickle cell trait blood: quality of the filtered product [J].
Amar, Karim Ould ;
Bourdonne, Olivier ;
Bruneau, Sylvie ;
Sellami, Fatiha ;
Richard, Pascale .
BLOOD TRANSFUSION, 2014, 12 :S193-S198
[3]   The rationale for abandoning sickle trait screening of red blood cell units for patients with sickle cell disease [J].
Aneke, J. ;
Barth, D. ;
Ward, R. ;
Pendergrast, J. ;
Kuo, K. ;
Cserti-Gazdewich, C. .
TRANSFUSION MEDICINE, 2019, 29 (06) :466-467
[4]   Apolipoprotein J/Clusterin Is a Novel Structural Component of Human Erythrocytes and a Biomarker of Cellular Stress and Senescence [J].
Antonelou, Marianna H. ;
Kriebardis, Anastasios G. ;
Stamoulis, Konstantinos E. ;
Trougakos, Ioannis P. ;
Papassideri, Issidora S. .
PLOS ONE, 2011, 6 (10)
[5]   Duration of red blood cells storage and outcome in critically ill patients [J].
Aubron, Cecile ;
Bailey, Michael ;
McQuilten, Zoe ;
Pilcher, David ;
Hegarty, Colin ;
Martinelli, Anthony ;
Magrin, Geoff ;
Irving, David ;
Cooper, D. Jamie ;
Bellomo, Rinaldo .
JOURNAL OF CRITICAL CARE, 2014, 29 (03) :476.e1-476.e8
[6]   Evaluation of a point-of-care method for screening blood donors for sickle cell status [J].
Badawi, Maha ;
Garoot, Sara ;
Tahlawi, Mofida ;
Hindawi, Salwa ;
Adam, Soheir .
TRANSFUSION, 2020, 60 :S10-S14
[7]   A broad diversity in oxygen affinity to haemoglobin [J].
Balcerek, Bjoern ;
Steinach, Mathias ;
Lichti, Julia ;
Maggioni, Martina A. ;
Becker, Philipp N. ;
Labes, Robert ;
Gunga, Hanns-Christian ;
Persson, Pontus B. ;
Faehling, Michael .
SCIENTIFIC REPORTS, 2020, 10 (01)
[8]  
Ballard HS, 1997, ALCOHOL HEALTH RES W, V21, P42
[9]   Iron-deficient erythropoiesis in blood donors and red blood cell recovery after transfusion: initial studies with a mouse model [J].
Bandyopadhyay, Sheila ;
Brittenham, Gary M. ;
Francis, Richard O. ;
Zimring, James C. ;
Hod, Eldad A. ;
Spitalnik, Steven L. .
BLOOD TRANSFUSION, 2017, 15 (02) :158-164
[10]   Lipaemic plasma induces haemolysis in resuspended red cell concentrate [J].
Bashir, S. ;
Wiltshire, M. ;
Cardigan, R. ;
Thomas, S. .
VOX SANGUINIS, 2013, 104 (03) :218-224