Reactive oxygen species elevations in human immune cell subsets during sepsis are mitigated by norepinephrine and N-acetylcysteine

ROS levels are elevated in specific PBMC subsets in sepsis, particularly CD3+ T cells and CD14+ monocytes. NE and NAC reduced ROS accumulation <i>in vitro</i>, supporting their potential role as redox modulators. These findings warrant further mechanistic investigation into immune redox regulation in sepsis.

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Publication Details

Journal
World Journal of Critical Care Medicine
Published
2025-11-28
DOI
https://doi.org/10.5492/wjccm.v14.i4.108638
Citations
1
Primary Topic
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Type
article
Field-Weighted Citation Impact
0.80
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article

Reactive oxygen species elevations in human immune cell subsets during sepsis are mitigated by norepinephrine and N-acetylcysteine

Drashya Sharma, David J. Farrar, Seth Kirby, Joby Thoppil et al.
1 citations
World Journal of Critical Care Medicine
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
0.80
article

Reactive oxygen species elevations in human immune cell subsets during sepsis are mitigated by norepinephrine and N-acetylcysteine

Drashya Sharma, David J. Farrar, Seth Kirby, Joby Thoppil, Angela B Mobley, D. Mark Courtney
article en
1 citations

Abstract

ROS levels are elevated in specific PBMC subsets in sepsis, particularly CD3+ T cells and CD14+ monocytes. NE and NAC reduced ROS accumulation <i>in vitro</i>, supporting their potential role as redox modulators. These findings warrant further mechanistic investigation into immune redox regulation in sepsis.

World Journal of Critical Care MedicineVol. 14(4)
The University of Texas Southwestern Medical Center (US)
Openalex Percentile: Top 21%
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
0.80
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