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Therapeutic effects of hydrogen on chronic graft-versus-host disease.

水素が慢性移植片対宿主病に及ぼす効果:マウスモデルを用いた検討

animal study injection / infusion positive

Abstract

Chronic graft-versus-host disease (cGVHD) represents a leading cause of non-relapse mortality following allogeneic hematopoietic stem cell transplantation, with inflammatory cytokine dysregulation and fibrosis as central pathogenic drivers. Using an MHC-incompatible murine bone marrow transplantation model, this study examined whether hydrogen-rich saline administration could mitigate cGVHD. Survival rates and skin lesion severity were monitored after transplantation. Mice receiving hydrogen-rich saline showed improved survival and reduced skin pathology compared with controls. These findings extend prior observations on hydrogen in acute GVHD to the chronic form, suggesting that the anti-inflammatory, antioxidant, and anti-fibrotic properties of molecular hydrogen may contribute to beneficial outcomes in cGVHD.

Mechanism

Molecular hydrogen is proposed to suppress cGVHD pathology by counteracting inflammatory cytokine imbalance and tissue fibrosis through its anti-inflammatory, antioxidant, and anti-fibrotic properties.

Bibliographic

Authors
Qian L, Liu X, Shen J, Zhao D, Yin W
Journal
J Cell Mol Med
Year
2017
PMID
28374556
DOI
10.1111/jcmm.13155
PMC
PMC5618705

Tags

Disease:移植片対宿主病 Delivery:点滴投与 Mechanism:抗酸化酵素 免疫調節 炎症抑制 脂質過酸化 酸化ストレス

Delivery context

Intravenous hydrogen-saline infusion is a clinic-only route and is not viable for everyday self-administration. For routine hydrogen intake, inhalation is the most practical route, but inhalation carries explosion risk and concentration matters (empirical LFL of 10%; high-concentration 66% / 100% devices are not recommended).

Safety notes

Intravenous hydrogen-saline infusion is a clinic-only route and is not viable for everyday self-administration. For routine hydrogen intake, inhalation is the most practical route, but inhalation carries explosion risk and concentration matters (empirical LFL of 10%; high-concentration 66% / 100% devices are not recommended).

See also:

Other papers on the same disease / condition

Cite as: H2 Papers — PMID 28374556. https://h2-papers.org/en/papers/28374556
Source: PubMed PMID 28374556