Hydrogenology
Hydrogenology editorial study record

Molecular Hydrogen as a Promising Therapy Could Be Linked With Increased Resting Treg Cells or Decreased Fas+ T Cell Subsets in a IgG4-PF-ILD Patient: A Case Report

Lui SW, Lu JW, Ho YJ, Tang SE, Ko KH, Hsieh TY, Liu FC. · In Vivo. 2024;38(3):1512-1518.

HumanOther formsPublished 2024
Study record, not medical adviceThis page reports one source and Hydrogenology’s source-text extraction. It does not establish that molecular hydrogen is effective, safe or appropriate for any person. Human, animal and laboratory evidence must not be treated as equivalent.
Source and classification

What kind of evidence is this?

Evidence stream

Human

Reported design

Single-patient case report without a control group

Research topic

Respiratory health

Administration classification

Other forms

Study result signal

Not reported in this record.

Outcome type

Not reported in this record.

Reported in the source

Methods at a glance

Population or model

An 85-year-old woman with suspected IgG4-related progressive fibrosing interstitial lung disease, hospital-acquired pneumonia, tracheostomy and mechanical-ventilator dependence after multiple concomitant treatments.

Sample

One patient; no comparator and no blinded outcome assessment.

Duration

Clinical changes were described through day 23 after H₂ initiation; the article does not provide a controlled long-term follow-up.

Intervention

One oral PURE HYDROGEN capsule daily, added to ongoing intensive-care treatment from 12 May 2023.

Hydrogen form

Oral hydrogen-generating capsule — not inhaled H₂ and not Brown's gas.

H₂ specification

Each capsule contained 170 mg hydrogen-rich coral calcium; the authors equated its stated hydrogen content with 24 × 200 mL cups of water at 1,200 ppb (0.6 mM). This manufacturer-style equivalence was reported by the source and was not independently validated by Hydrogenology.

H₂ flow

Not applicable — oral capsule, not gas inhalation.

O₂ delivered with H₂

No O₂ was co-delivered as part of the H₂ intervention.

Comparator

No formal comparator; the report describes the clinical course before and after H₂ was added while other ICU treatments and spontaneous change remained possible explanations.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Chest radiographs, ventilator-free time, clinical course, adverse events, peripheral-blood immune phenotypes, nucleosome count and hemoglobin.

Reported result

The authors reported radiographic improvement by days 2-4, communication by day 7, 10 ventilator-free hours on day 14 and 18 hours on day 23, with no observed adverse event. Resting Treg cells increased and Fas-positive helper/cytotoxic T-cell subsets decreased. Causation cannot be separated from concomitant care or natural recovery in this one-patient report.

Results-extraction completeness

The complete free PMC article was checked for the patient's course, product and schedule, reported outcomes, limitations, acknowledgements, funding and conflict declaration.

A reported association, difference or mechanism is not automatically a clinical benefit. Null findings, outcome type, study design and precision all matter.

Interpretation limits

Cautions and applicability

Design and reporting cautions

One uncontrolled case with suspected rather than biopsy-confirmed IgG4-related disease, numerous prior and concomitant treatments, severe infection and no way to attribute improvement to H₂. The commercial capsule was purchased from HoHo Biotech; the authors declared no conflicts. Taiwanese public/institutional grants supported the work.

Applies directly to

Describes one critically ill patient and cannot establish effectiveness, safety or a generalizable dose for PF-ILD.

Preliminary appraisal framework

Not reported in this record.

Preliminary risk-of-bias status

Not reported in this record.

Appraisal rationale

Not reported in this record.

No single-study GRADE certainty rating is assigned. Certainty is assessed by important outcome across a complete eligible evidence set, not by attaching a final grade to one source.

Provenance

Sources and record status

Identifiers

PMID: 38688598 · DOI: 10.21873/invivo.13600

Publisher access

Free full article in PubMed Central.

Extraction basis

Complete PMC article and PubMed metadata; full-text extraction checked 9 August 2026.

Record revision

2026-08-10