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Reticulocytes in donor blood units enhance red blood cell alloimmunization.

Authors :
Thomas TA
Qiu A
Kim CY
Gordy DE
Miller A
Tredicine M
Dzieciatkowska M
Dei Zotti F
Hod EA
D'Alessandro A
Zimring JC
Spitalnik SL
Hudson KE
Source :
Haematologica [Haematologica] 2023 Oct 01; Vol. 108 (10), pp. 2639-2651. Date of Electronic Publication: 2023 Oct 01.
Publication Year :
2023

Abstract

Although red blood cell (RBC) transfusions save lives, some patients develop clinically-significant alloantibodies against donor blood group antigens, which then have adverse effects in multiple clinical settings. Few effective measures exist to prevent RBC alloimmunization and/or eliminate alloantibodies in sensitized patients. Donor-related factors may influence alloimmunization; thus, there is an unmet clinical need to identify which RBC units are immunogenic. Repeat volunteer blood donors and donors on iron supplements have elevated reticulocyte counts compared to healthy non-donors. Early reticulocytes retain mitochondria and other components, which may act as danger signals in immune responses. Herein, we tested whether reticulocytes in donor RBC units could enhance RBC alloimmunization. Using a murine model, we demonstrate that transfusing donor RBC units with increased reticulocyte frequencies dose-dependently increased RBC alloimmunization rates and alloantibody levels. Transfusing reticulocyte-rich RBC units was associated with increased RBC clearance from the circulation and a robust proinflammatory cytokine response. As compared to previously reported post-transfusion RBC consumption patterns, erythrophagocytosis from reticulocyte-rich units was increasingly performed by splenic B cells. These data suggest that reticulocytes in a donated RBC unit impact the quality of blood transfused, are targeted to a distinct compartment, and may be an underappreciated risk factor for RBC alloimmunization.

Details

Language :
English
ISSN :
1592-8721
Volume :
108
Issue :
10
Database :
MEDLINE
Journal :
Haematologica
Publication Type :
Academic Journal
Accession number :
37078267
Full Text :
https://doi.org/10.3324/haematol.2023.282815