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  2. 生命科學院
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Please use this identifier to cite or link to this item: http://scholars.ntou.edu.tw/handle/123456789/26249
Title: Adjuvant Molecular Hydrogen Therapy in SLE-associated Pulmonary Arterial Hypertension: A Case Report on Immunomodulatory Effects on Regulatory and Effector Lymphocytes
Authors: Liu, Chin
Lu, Jeng-Wei 
Wu, Chun-Hsien
Ho, Yi-Jung
Lui, Shan-Wen
Hsieh, Ting-Yu
Wang, Kuang-Yih
Liu, Feng-Cheng
Keywords: Systemic lupus erythematosus;pulmonary arterial hypertension;immune modulation
Issue Date: 2026
Publisher: INT INST ANTICANCER RESEARCH
Journal Volume: 40
Journal Issue: 1
Start page/Pages: 10
Source: IN VIVO
Abstract: 
Background/Aim: Pulmonary arterial hypertension (PAH) is a significant and challenging complication for patients with systemic lupus erythematosus (SLE). It is thought to arise from immune dysregulation and vascular remodeling, ultimately leading to progressive right heart failure. Molecular hydrogen therapy, a selective antioxidant and antiinflammatory agent, may modulate the immune responses seen in autoimmune diseases. This case report details the use of adjuvant hydrogen capsule therapy in a patient with SLE with PAH, suggesting its potential as a novel approach for this difficult clinical condition. Case Report: A 42-year-old Taiwanese woman with SLE-PAH received hydrogen capsule therapy, during which serial immunophenotyping revealed dynamic changes in suppressive markers including programmed cell death protein 1(PD1) and Fas cell surface death receptor (FAS), as well as regulatory T-and B-cell subsets. Notably, the populations of double negative and class-switched memory B-cells decreased during therapy, suggesting durable immune suppression. These results support the effect of hydrogen capsule therapy in achieving immune tolerance and inflammation modulation. Conclusion: This case study suggests that molecular hydrogen therapy may be a promising treatment for patients with SLE-PAH, particularly due to its immunomodulatory effects.
URI: http://scholars.ntou.edu.tw/handle/123456789/26249
ISSN: 0258-851X
DOI: 10.21873/invivo.14220
Appears in Collections:生命科學暨生物科技學系

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