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Adipose-derived stem cell exosomes for treatment of dupilumab-related facial redness in patients with atopic dermatitisopen access

Authors
Han, Hye SungKoh, Young GueHong, Jun KiRoh, Yoon JinSeo, Seong JunPark, Kui Young
Issue Date
Dec-2023
Publisher
TAYLOR & FRANCIS LTD
Keywords
Atopic dermatitis; dupilumab; dupilumab facial redness; exosome; filaggrin; inflammation
Citation
JOURNAL OF DERMATOLOGICAL TREATMENT, v.34, no.1
Journal Title
JOURNAL OF DERMATOLOGICAL TREATMENT
Volume
34
Number
1
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/71678
DOI
10.1080/09546634.2023.2220444
ISSN
0954-6634
1471-1753
Abstract
Background Dupilumab facial redness (DFR) is a side effect of dupilumab treatment that has only been recently reported. We previously reported on two patients with DFR who were successfully treated with a topical formulation containing human adipose tissue-derived mesenchymal stem cell-derived exosomes (ASCEs). Objectives The study aimed to evaluate the efficacy and safety of ASCEs in DFR. Participants and methods We performed 12-week prospective study at single center. Twenty adult atopic dermatitis patients diagnosed with DFR were enrolled. They were treated with a topical application of the exosome formulation every week for five consecutive weeks. Results After exosome treatment, both the average investigator global assessment score and clinical erythema assessment scale scores decreased. 19 patients (95%) were satisfied with the treatment. Compared to baseline, erythema index at week 4 were decreased by 31, 27, 13, and 25 units on the forehead, chin, right and left cheek respectively. The analysis of stratum corneum samples revealed the expression of IL-1 alpha and human thymic stromal lymphopoietin was suppressed after exosome treatment, whereas filaggrin and vascular endothelial growth factor expression increased. Conclusions This study suggests topical formulation containing ASCEs can alleviate DFR by downregulating local inflammation and restoring skin barrier function.
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의과대학 (의학부(임상-서울))
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