Abstract |
Phototherapy with 311-nm narrowband-UVB (NBUVB) is an effective adjuvant treatment modality for atopic dermatitis (AD). In this study, we evaluated the therapeutic effect of the newly developed gain-switched 311-nm Ti: Sapphire laser device using a NC/Nga mouse AD model. A total number of 50 mice were used in this study. Atopic dermatitis (AD) was induced in mice by exposure to Dermatophagoides farina. These, NC/Nga mice were then treated with conventional 311-nm NBUVB or the newly developed gain-switched 311-nm Ti: Sapphire laser. The clinical features, dermatitis severity scores, and scratching behavior were assessed. In addition, serologic analyses including inflammatory cytokines and histological analyses were performed. Gain-switched 311-nm Ti: Sapphire laser improved the AD-like skin lesions, severity, and symptoms of AD in the NC/Nga mouse model. This new laser also modulated the immune response found in the AD model, including hyper- IgE, upregulated Th2 cytokines, and the Th2-mediated allergic inflammatory reaction. Gain-switched 311-nm Ti: Sapphire laser shows therapeutic promise via an immune-modulation mechanism in an AD mouse model. These data suggest that gain-switched 311-nm Ti: Sapphire laser may be useful as a targeted phototherapy modality for AD.
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Authors | Sun Young Choi, Chang Taek Oh, Tae-Rin Kwon, Hyun Jung Kwon, Eun Ja Choi, Yu-Jin Jang, Hye Sung Kim, Hong Chu, Seog Kyun Mun, Myeung Nam Kim, Beom Joon Kim |
Journal | Lasers in medical science
(Lasers Med Sci)
Vol. 31
Issue 7
Pg. 1437-45
(Sep 2016)
ISSN: 1435-604X [Electronic] England |
PMID | 27394442
(Publication Type: Journal Article)
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Chemical References |
- Cytokines
- Inflammation Mediators
- Immunoglobulin E
- Aluminum Oxide
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Topics |
- Aluminum Oxide
(chemistry)
- Animals
- Cytokines
(biosynthesis)
- Dermatitis, Atopic
(radiotherapy)
- Disease Models, Animal
- Hypersensitivity
(immunology, pathology)
- Immunoglobulin E
(biosynthesis)
- Inflammation
(immunology, pathology)
- Inflammation Mediators
(metabolism)
- Laser Therapy
- Mice
- Skin
(pathology, radiation effects)
- Th2 Cells
(immunology)
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