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  1. National Taiwan Ocean University Research Hub
  2. 生命科學院
  3. 生命科學暨生物科技學系
請用此 Handle URI 來引用此文件: http://scholars.ntou.edu.tw/handle/123456789/26150
DC 欄位值語言
dc.contributor.authorLiu, Hinen_US
dc.contributor.authorLu, Jeng - Weien_US
dc.contributor.authorWu, Chun - Hsienen_US
dc.contributor.authorHo, Yi - Jungen_US
dc.contributor.authorLui, Shan - Wenen_US
dc.contributor.authorHsieh, Ting - Yuen_US
dc.contributor.authorWang, Kuang - Yihen_US
dc.contributor.authorLiu, Feng - Chengen_US
dc.date.accessioned2026-03-12T03:20:15Z-
dc.date.available2026-03-12T03:20:15Z-
dc.date.issued2025/11/1-
dc.identifier.issn0258-851X-
dc.identifier.urihttp://scholars.ntou.edu.tw/handle/123456789/26150-
dc.description.abstractBackground/Aim: Pulmonary arterial hypertension (PAH) is a severe complication of systemic lupus erythematosus (SLE), marked by vascular remodeling, immune dysregulation, and progressive right heart failure. Molecular hydrogen therapy, a selective antioxidant and anti-inflammatory agent, has the capacity to modulate immune responses in these autoimmune disease patients. This case report details the clinical improvement in an SLE patient with PAH after starting adjunctive hydrogen capsule therapy, highlighting its potential as a novel approach for this challenging complication. Case Report: A 45-year-old Taiwanese woman with SLE-PAH who received hydrogen capsule therapy, during which serial immunophenotyping revealed dynamic changes in T cell exhaustion markers, regulatory T cell (Treg) subsets, and regulatory B cells (Breg). Notably, KLRG1+ T cells and CD39+Helios- Tregs were suppressed during therapy but rebounded after cessation, suggesting transient immune suppressing followed by regulatory rebalancing. Bregs also showed a similar pattern, declining during therapy and recovering after discontinuation. Conclusion: These findings suggest a biphasic immunomodulatory effect of hydrogen therapy, that is, initially dampening immune activation, followed by a regulatory rebound after hydrogen therapy.en_US
dc.language.isoEnglishen_US
dc.publisherINT INST ANTICANCER RESEARCHen_US
dc.relation.ispartofIN VIVOen_US
dc.subjectSystemic lupus erythematosusen_US
dc.subjectpulmonary arterial hypertensionen_US
dc.subjectimmune modulationen_US
dc.titleDynamic Immunomodulation by Hydrogen Capsule Therapy in SLE-associated Pulmonary Arterial Hypertension: A Case Reporten_US
dc.typejournal articleen_US
dc.identifier.doi10.21873/invivo.14165-
dc.identifier.isiWOS:001607887600010-
dc.relation.journalvolume39en_US
dc.relation.journalissue6en_US
dc.relation.pages9en_US
dc.identifier.eissn1791-7549-
item.cerifentitytypePublications-
item.fulltextno fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.languageiso639-1English-
item.openairetypejournal article-
crisitem.author.deptDepartment of Bioscience and Biotechnology-
crisitem.author.deptCollege of Life Sciences-
crisitem.author.deptNational Taiwan Ocean University,NTOU-
crisitem.author.parentorgCollege of Life Sciences-
crisitem.author.parentorgNational Taiwan Ocean University,NTOU-
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