Biological effects of a new ultraviolet A(1)prototype based on light-emitting diodes on the treatment of localized scleroderma

Arndt, Stephanie and Lissner, Clara and Unger, Petra and Baeumler, Wolfgang and Berneburg, Mark and Karrer, Sigrid (2020) Biological effects of a new ultraviolet A(1)prototype based on light-emitting diodes on the treatment of localized scleroderma. EXPERIMENTAL DERMATOLOGY, 29 (12). pp. 1199-1208. ISSN 0906-6705, 1600-0625

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Abstract

Ultraviolet A(1)(UVA(1)) phototherapy (spectral range 340-400 nm) is a well-established treatment option for various skin diseases such as localized scleroderma. Recent improvements of conventional UVA(1)light sources (metal-halide or fluorescent lamps) have brought attention to a new light-emitting diode (LED) technology with remarkable advantages in handling and clinical routine. This study provides a preclinical histological and molecular evaluation of an LED-based UVA(1)prototype with a narrower spectral range (360-400 nm) for treating localized scleroderma. Scleroderma mouse models and fibroblasts in vitro were exposed to LED-based UVA(1)phototherapy or to irradiation with a commercially available metal-halide lamp emitting low-dose (20, 40 J/cm(2)), medium-dose (60 J/cm(2)) and high-dose (80, 100 J/cm(2)) UVA(1)light. Both UVA(1)light sources affected inflammatory genes (IL-1 alpha and IL-6) and growth factors (TGFss-1 and TGFss-2). Increased collagen type 1 was reduced after UVA(1)phototherapy. Matrix metalloproteinase-1 was more enhanced after a medium dose of LED-based UVA(1)phototherapy than after conventional treatment. In vivo, dermal thickness and the amount of collagen were reduced after both treatment methods. Remarkably, myofibroblasts were more effectively reduced by a medium dose of LED-based UVA(1)phototherapy. The study indicates that LED-based UVA(1)phototherapy yields similar or even better results than conventional treatment. In terms of biosafety and patient comfort, LED-based UVA(1)phototherapy offers clear advantages over conventional treatment because of the use of a narrower and less harmful UVA(1)spectrum, less heat generation and shorter treatment times at the same irradiation intensity. Clinical studies are required to confirm these results in patients with localized scleroderma.

Item Type: Article
Uncontrolled Keywords: GROWTH-FACTOR-BETA; HUMAN DERMAL FIBROBLASTS; BLEOMYCIN-INDUCED SCLERODERMA; UVA(1) RADIATION-THERAPY; SMOOTH MUSCLE ACTIN; A1 PHOTOTHERAPY; SINGLET OXYGEN; ANIMAL-MODEL; TGF-BETA; MATRIX METALLOPROTEINASE-1; extracellular matrix; fibroblasts; LED-based UVA(1); localized scleroderma; phototherapy
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Dermatologie und Venerologie
Depositing User: Dr. Gernot Deinzer
Date Deposited: 18 Mar 2021 07:42
Last Modified: 18 Mar 2021 07:42
URI: https://pred.uni-regensburg.de/id/eprint/44194

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