Abstract
Red blood cells (RBC) from patients with sickle cell disease (SCD) are continuously exposed to high levels of oxidative stress, which impacts RBC deformability. In this study, we applied a novel technique (oxidantscan) to measure deformability of RBCs under shear stress while exposed to oxidative stress. Using RBCs collected from a cohort of patients with SCD and healthy volunteers, we measured different parameters including T-POD (Time to initiate Oxidant-induced change in Deformability) and EIMin (the minimum deformability reached during the test). T-POD was significantly shorter in patients with HbSS ( n = 21, 729 ± 410 s) and HbSC ( n = 19, 1031 ± 225 s) when compared to healthy controls ( n = 20, 1739 ± 328 s, p < 0.05). Also EIMin was significantly lower in patients with HbSS (0.26 ± 0.10) and HbSC (0.30 ± 0.10) compared to healthy controls (0.54 ± 0.02). These results indicate that RBCs from patients with SCD are more susceptible to oxidative stress, which can be measured in a reproducible and quantifiable way. We also demonstrate that Oxidantscan outcome parameters correlated with sickling behavior and markers of hemolysis, indicating a possible link between these key pathophysiological features and the ability to withstand oxidative stress (all p < 0.05). Finally, we provide preliminary evidence for the potential of this technique to evaluate antioxidant therapy with l -glutamine as SCD RBCs showed a significant improvement in T-POD (11.5 %, p = 0.01) and EIMin (46.9 %, p = 0.03) upon ex vivo treatment with l -glutamine. The Oxidantscan is a promising technique for evaluating the response of SCD RBCs to oxidative stress, providing new insights in disease pathophysiology and potential novel treatment strategies.
| Original language | English |
|---|---|
| Article number | 102967 |
| Number of pages | 9 |
| Journal | Blood Cells, Molecules, & Diseases |
| Volume | 117 |
| Early online date | 19 Nov 2025 |
| DOIs | |
| Publication status | Published - Mar 2026 |
Keywords
- Oxidative stress
- Oxygen gradient ektacytometry
- Red blood cell
- Sickle cell disease
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