Quality assessment of red blood cell concentrates from blood donors at the extremes of the age spectrum: The BEST collaborative study.


Journal

Transfusion
ISSN: 1537-2995
Titre abrégé: Transfusion
Pays: United States
ID NLM: 0417360

Informations de publication

Date de publication:
08 2023
Historique:
revised: 07 05 2023
received: 18 02 2023
accepted: 04 06 2023
medline: 14 8 2023
pubmed: 30 6 2023
entrez: 30 6 2023
Statut: ppublish

Résumé

Blood donors at the extremes of the age spectrum (16-19 years vs. ≥75 years) are characterized by increased risks of iron deficiency and anemia, and are often underrepresented in studies evaluating the effects of donor characteristics on red blood cells (RBC) transfusion effectiveness. The aim of this study was to conduct quality assessments of RBC concentrates from these unique age groups. We characterized 150 leukocyte-reduced (LR)-RBCs units from 75 teenage donors, who were matched by sex, and ethnicity with 75 older donors. LR-RBC units were manufactured at three large blood collection centers in the USA and Canada. Quality assessments included storage hemolysis, osmotic hemolysis, oxidative hemolysis, osmotic gradient ektacytometry, hematological indices, and RBC bioactivity. RBC concentrates from teenage donors had smaller (9%) mean corpuscular volume and higher (5%) RBC concentration compared with older donors counterparts. Stored RBCs from teenage donors exhibited increased susceptibility to oxidative hemolysis (>2-fold) compared with RBCs from older donors. This was observed at all testing centers independent of sex, storage duration, or the type of additive solution. RBCs from teenage male donors had increased cytoplasmatic viscosity and lower hydration compared with older donor RBCs. Evaluations of RBC supernatant bioactivity suggested that donor age was not associated with altered expression of inflammatory markers (CD31, CD54, and IL-6) on endothelial cells. The reported findings are likely intrinsic to RBCs and reflect age-specific changes in RBC antioxidant capacity and physical characteristics that may impact RBC survival during cold storage and after transfusion.

Sections du résumé

BACKGROUND
Blood donors at the extremes of the age spectrum (16-19 years vs. ≥75 years) are characterized by increased risks of iron deficiency and anemia, and are often underrepresented in studies evaluating the effects of donor characteristics on red blood cells (RBC) transfusion effectiveness. The aim of this study was to conduct quality assessments of RBC concentrates from these unique age groups.
STUDY DESIGN
We characterized 150 leukocyte-reduced (LR)-RBCs units from 75 teenage donors, who were matched by sex, and ethnicity with 75 older donors. LR-RBC units were manufactured at three large blood collection centers in the USA and Canada. Quality assessments included storage hemolysis, osmotic hemolysis, oxidative hemolysis, osmotic gradient ektacytometry, hematological indices, and RBC bioactivity.
RESULTS
RBC concentrates from teenage donors had smaller (9%) mean corpuscular volume and higher (5%) RBC concentration compared with older donors counterparts. Stored RBCs from teenage donors exhibited increased susceptibility to oxidative hemolysis (>2-fold) compared with RBCs from older donors. This was observed at all testing centers independent of sex, storage duration, or the type of additive solution. RBCs from teenage male donors had increased cytoplasmatic viscosity and lower hydration compared with older donor RBCs. Evaluations of RBC supernatant bioactivity suggested that donor age was not associated with altered expression of inflammatory markers (CD31, CD54, and IL-6) on endothelial cells.
CONCLUSIONS
The reported findings are likely intrinsic to RBCs and reflect age-specific changes in RBC antioxidant capacity and physical characteristics that may impact RBC survival during cold storage and after transfusion.

Identifiants

pubmed: 37387566
doi: 10.1111/trf.17471
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1506-1518

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2023 AABB.

Références

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Auteurs

Marc Cloutier (M)

Affaires Médicales et Innovation, Héma-Québec, Québec, Québec, Canada.

Fabrice Cognasse (F)

Research Department, F-42023, Établissement Français du Sang Auvergne-Rhône-Alpes, Saint-Étienne, France.
INSERM, U 1059 SAINBIOSE, Université Jean Monnet Saint-Étienne, Mines Saint Etienne, F-42023, Saint-Etienne, France.

Ana Paula Hitomi Yokoyama (APH)

Hemotherapy and Cell Therapy Department, Hospital Israelita Albert Einstein, São Paulo, Brazil.

Kelsey Hazegh (K)

Vitalant Research Institute, Denver, Colorado, USA.

Olga Mykhailova (O)

Innovation and Portfolio Management, Canadian Blood Services, Edmonton, Alberta, Canada.

Mackenzie Brandon-Coatham (M)

Innovation and Portfolio Management, Canadian Blood Services, Edmonton, Alberta, Canada.

Hind Hamzeh-Cognasse (H)

Research Department, F-42023, Établissement Français du Sang Auvergne-Rhône-Alpes, Saint-Étienne, France.
INSERM, U 1059 SAINBIOSE, Université Jean Monnet Saint-Étienne, Mines Saint Etienne, F-42023, Saint-Etienne, France.

Jose Mauro Kutner (JM)

Hemotherapy and Cell Therapy Department, Hospital Israelita Albert Einstein, São Paulo, Brazil.

Jason P Acker (JP)

Innovation and Portfolio Management, Canadian Blood Services, Edmonton, Alberta, Canada.
Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.

Tamir Kanias (T)

Vitalant Research Institute, Denver, Colorado, USA.
Department of Pathology, University of Colorado Denver Anschutz Medical Campus, Aurora, Colorado, USA.

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