Longitudinal <i>In Vivo</i> Immunophenotyping of Regulatory T Cells Following Adjunctive Molecular Hydrogen Therapy in Systemic Lupus Erythematosus

<h3>Background/Aim:</h3> Regulatory T cells (Tregs) are pivotal for maintaining immune tolerance, yet their dynamic changes during the transition from active disease to remission in systemic lupus erythematosus (SLE) remain unclear. We assessed whether specific Treg subpopulations can serve as biomarkers of clinical recovery. <h3>Patients and Methods:</h3> We conducted longitudinal immunophenotyping in eight patients with SLE across healthy, active, and stable disease states tracking CD3<sup>+</sup>CD4<sup>+</sup>CD25^highCD127^low/<sup>−</sup>FoxP3<sup>+</sup> Tregs, natural Tregs, and activated Tregs. <h3>Results:</h3> In contrast to static deficiency models, our longitudinal analysis revealed a distinct dynamic pattern: FoxP3<sup>+</sup> Tregs particularly natural and activated subsets expanded during active disease, consistent with a compensatory response, and contracted toward baseline with clinical stabilization. <h3>Conclusion:</h3> The transient expansion and subsequent normalization of Treg subsets distinguish active inflammation from stable remission, serving as a potential immunophenotypic signature of successful immune resetting in SLE.

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Publication Details

Journal
In Vivo
Published
2026-06-30
DOI
https://doi.org/10.21873/invivo.14412
Primary Topic
Hydrogen's biological and therapeutic effects
Type
article
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article

Longitudinal In Vivo Immunophenotyping of Regulatory T Cells Following Adjunctive Molecular Hydrogen Therapy in Systemic Lupus Erythematosus

KUANG-YIH WANG, CHIN LIU, TING-YU HSIEH, SHAN-WEN LUI et al.
In Vivo
Hydrogen's biological and therapeutic effects
article

Longitudinal In Vivo Immunophenotyping of Regulatory T Cells Following Adjunctive Molecular Hydrogen Therapy in Systemic Lupus Erythematosus

KUANG-YIH WANG, CHIN LIU, TING-YU HSIEH, SHAN-WEN LUI, FENG-CHENG LIU, YING-CHEN CHEN, WUN-LONG JHENG, YI-JUNG HO, JENG-WEI LU
article en

Abstract

<h3>Background/Aim:</h3> Regulatory T cells (Tregs) are pivotal for maintaining immune tolerance, yet their dynamic changes during the transition from active disease to remission in systemic lupus erythematosus (SLE) remain unclear. We assessed whether specific Treg subpopulations can serve as biomarkers of clinical recovery. <h3>Patients and Methods:</h3> We conducted longitudinal immunophenotyping in eight patients with SLE across healthy, active, and stable disease states tracking CD3<sup>+</sup>CD4<sup>+</sup>CD25^highCD127^low/<sup>−</sup>FoxP3<sup>+</sup> Tregs, natural Tregs, and activated Tregs. <h3>Results:</h3> In contrast to static deficiency models, our longitudinal analysis revealed a distinct dynamic pattern: FoxP3<sup>+</sup> Tregs particularly natural and activated subsets expanded during active disease, consistent with a compensatory response, and contracted toward baseline with clinical stabilization. <h3>Conclusion:</h3> The transient expansion and subsequent normalization of Treg subsets distinguish active inflammation from stable remission, serving as a potential immunophenotypic signature of successful immune resetting in SLE.

In VivoVol. 40(4)
University of Copenhagen (DK), Shizuoka University (JP), Hamamatsu University (JP), National Taiwan Ocean University (TW), Rigshospitalet (DK), Chang Gung Memorial Hospital (TW), Taichung Veterans General Hospital (TW), Linkou Chang Gung Memorial Hospital (TW), Hualien Tzu Chi Medical Center (TW), National Defense Medical Center (TW)
Good health and well-being
Openalex Percentile: Top 7%
Hydrogen's biological and therapeutic effects
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