Non-thermal argon plasma therapy alleviates atopic dermatitis by reducing keratinocyte oxidative stress
Authors:
- Young Joon ParkYPYoung Joon Park
- Mei HuangMHMei Huang
- Yun Sang LeeYLYun Sang Lee
- Han-Seul KimHKHan-Seul Kim
- Hee Young KangHKHee Young Kang
- Chul-Ho KimCKChul-Ho Kim
Open Access
- 2 November 2026
- journal article
- Published by Springer Nature in Molecular Biomedicine
- Vol. 7 (1)
Abstract
Atopic dermatitis (AD) is a prevalent inflammatory skin disorder associated with a considerable disease burden. Despite the advent of biologics a substantial unmet need remains for effective treatment. We aimed to evaluate the effects of non-thermal argon plasma (NAP) in patients with mild-to-moderate AD. The Eczema Area Severity Index (EASI), Numeric Rating Scale (NRS), and Dermatology Life Quality Index (DLQI) were evaluated following AD treatment. 16 S rRNA sequencing was used to assess alterations in the skin microbiome. A mouse model of house dust mite (HDM)-induced AD was used to evaluate the effects of NAP on AD-like lesions, immune cell recruitment, and cytokine expression. Oxidative stress parameters and related molecular markers were analyzed after NAP treatment. NAP treatment led to a significant reduction in EASI, NRS, and DLQI scores compared with the sham group, reflecting an alleviation of AD symptoms and an enhancement in the quality of life. Microbiome analysis revealed significant alterations in the microbial diversity after NAP treatment. NAP ameliorated HDM-induced AD in mice, showing a decrease in epidermal thickness, immune cell recruitment, and the expression of key cytokines, particularly interleukin (IL)− 33, in keratinocytes. Furthermore, NAP treatment downregulated oxidative stress markers, corroborating the reduced IL-33 expression and underscoring the role of oxidative stress in AD pathology. Our study suggests the therapeutic potential of nonthermal plasma in the management of mild-to-moderate AD. Further extensive clinical trials are warranted to validate these findings and understand their long-term effects and implications. Trial registration : CRIS, KCT0008949, retrospectively registered on October 10, 2023, at https://cris.nih.go.kr/cris/search/detailSearch.do?seq=25713 .Keywords
Funding Information
- Korea Health Industry Development Institute (HR21C1003)
- Korea Health Industry Development Institute (RS-2024-00407544)
- Korea Health Industry Development Institute (RS-2024-00406579)
- Ministry of Environment (2021003350001)
- Ministry of Science, ICT and Future Planning (2023R1A2C3002835)
This publication has 28 references indexed in Scilit:
- Global, regional, and national burden of asthma and atopic dermatitis, 1990–2021, and projections to 2050: a systematic analysis of the Global Burden of Disease Study 2021The Lancet Respiratory Medicine, 2025
- Tralokinumab treatment improves the skin microbiota by increasing the microbial diversity in adults with moderate-to-severe atopic dermatitis: Analysis of microbial diversity in ECZTRA 1, a randomized controlled trialJournal of the American Academy of Dermatology, 2022
- Phase 2 randomized clinical trial of astegolimab in patients with moderate to severe atopic dermatitisJournal of Allergy and Clinical Immunology, 2022
- Efficacy and Safety of Dupilumab in Adolescents With Uncontrolled Moderate to Severe Atopic DermatitisJAMA Dermatology, 2020
- IL-33 stimulates human mast cell release of CCL5 and CCL2 via MAPK and NF-κB, inhibited by methoxyluteolinEuropean Journal of Pharmacology, 2019
- IL-33–Induced Atopic Dermatitis–Like Inflammation in Mice Is Mediated by Group 2 Innate Lymphoid Cells in Concert with BasophilsJournal of Investigative Dermatology, 2019
- Non-thermal plasma inhibits mast cell activation and ameliorates allergic skin inflammatory diseases in NC/Nga miceScientific Reports, 2019
- Association of Disease Severity With Skin Microbiome and Filaggrin Gene Mutations in Adult Atopic DermatitisJAMA Dermatology, 2018
- Long-term management of moderate-to-severe atopic dermatitis with dupilumab and concomitant topical corticosteroids (LIBERTY AD CHRONOS): a 1-year, randomised, double-blinded, placebo-controlled, phase 3 trialThe Lancet, 2017
- IL-33 and ST2 in Atopic Dermatitis: Expression Profiles and Modulation by Triggering FactorsJournal of Investigative Dermatology, 2012