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The Post-Storage Performance of RBCs from Beta-Thalassemia Trait Donors Is Related to Their Storability Profile.

Authors :
Anastasiadi AT
Paronis EC
Arvaniti VZ
Velentzas AD
Apostolidou AC
Balafas EG
Dzieciatkowska M
Kostomitsopoulos NG
Stamoulis K
Papassideri IS
D'Alessandro A
Kriebardis AG
Antonelou MH
Tzounakas VL
Source :
International journal of molecular sciences [Int J Mol Sci] 2021 Nov 13; Vol. 22 (22). Date of Electronic Publication: 2021 Nov 13.
Publication Year :
2021

Abstract

Blood donors with beta-thalassemia traits (βThal <superscript>+</superscript> ) have proven to be good "storers", since their stored RBCs are resistant to lysis and resilient against oxidative/proteotoxic stress. To examine the performance of these RBCs post-storage, stored βThal <superscript>+</superscript> and control RBCs were reconstituted in plasma donated from transfusion-dependent beta-thalassemic patients and healthy controls, and incubated for 24 h at body temperature. Several physiological parameters, including hemolysis, were evaluated. Moreover, labeled fresh/stored RBCs from the two groups were transfused in mice to assess 24 h recovery. All hemolysis metrics were better in the group of heterozygotes and distinguished them against controls in the plasma environment. The reconstituted βThal <superscript>+</superscript> samples also presented higher proteasome activity and fewer procoagulant extracellular vesicles. Transfusion to mice demonstrated that βThal <superscript>+</superscript> RBCs present a marginal trend for higher recovery, regardless of the recipient's immune background and the RBC storage age. According to correlation analysis, several of these advantageous post-storage characteristics are related to storage phenotypes, like the cytoskeleton composition, low cellular fragility, and enhanced membrane proteostasis that characterize stored βThal <superscript>+</superscript> RBCs. Overall, it seems that the intrinsic physiology of βThal <superscript>+</superscript> RBCs benefits them in conditions mimicking a recipient environment, and in the circulation of animal models; findings that warrant validation in clinical trials.

Details

Language :
English
ISSN :
1422-0067
Volume :
22
Issue :
22
Database :
MEDLINE
Journal :
International journal of molecular sciences
Publication Type :
Academic Journal
Accession number :
34830162
Full Text :
https://doi.org/10.3390/ijms222212281