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Immunomodulatory Effects of Molecular Hydrogen Therapy in Systemic Lupus Erythematosus With Pericarditis and Pleuritis: A Case Report.

全身性エリテマトーデスに伴う心膜炎・胸膜炎に対する分子状水素の免疫調節効果:症例報告

human case report not specified mixed

Abstract

A 49-year-old Taiwanese woman with systemic lupus erythematosus (SLE) complicated by pericarditis, pleuritis, and multi-organ involvement experienced recurrent disease flares despite conventional immunomodulatory management. In October 2024, molecular hydrogen supplementation was added as an adjunct intervention. Subsequent immunophenotypic analysis demonstrated notable shifts in immune cell populations: a declining trend in Tr1 regulatory cells alongside increasing proportions of naive Treg cells, Fas-expressing B cell subsets, and transitional B cells. These findings suggest that molecular hydrogen may influence immune cell dynamics in autoimmune conditions. The authors note that broader clinical studies are needed to establish efficacy and safety profiles before definitive conclusions can be drawn.

Mechanism

Molecular hydrogen's antioxidant, anti-inflammatory, and antiapoptotic properties are proposed to underlie observed shifts in immune cell composition, including reduced Tr1 cells and increased naive Treg cells, Fas-expressing B cell subsets, and transitional B cells in an SLE patient.

Bibliographic

Authors
Tu TH, Lu J, Ho YJ, Lui SW, Hsieh TY, Wang K, et al.
Journal
In Vivo
Year
2025
PMID
40877145
DOI
10.21873/invivo.14103
PMC
PMC12396063

Tags

Mechanism:アポトーシス抑制 免疫調節 炎症抑制 酸化ストレス

Delivery context

The delivery route is not clearly identifiable from this paper. For hydrogen intake, inhalation is the most efficient route; inhalation, however, carries explosion risk (empirical LFL of 10%; high-concentration devices are not recommended).

Safety notes

The delivery route is not clearly identifiable from this paper. For hydrogen intake, inhalation is the most efficient route; inhalation, however, carries explosion risk (empirical LFL of 10%; high-concentration devices are not recommended).

See also:

Cite as: H2 Papers — PMID 40877145. https://h2-papers.org/en/papers/40877145
Source: PubMed PMID 40877145