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

J Dermatolog Treat. 2023 Dec;34(1):2220444. doi: 10.1080/09546634.2023.2220444.

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-1α 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.

Keywords: Atopic dermatitis; dupilumab; dupilumab facial redness; exosome; filaggrin; inflammation.

MeSH terms

  • Adult
  • Dermatitis, Atopic* / drug therapy
  • Dermatitis, Atopic* / metabolism
  • Double-Blind Method
  • Erythema
  • Exosomes* / metabolism
  • Humans
  • Prospective Studies
  • Severity of Illness Index
  • Stem Cells / metabolism
  • Treatment Outcome
  • Vascular Endothelial Growth Factor A

Substances

  • dupilumab
  • Vascular Endothelial Growth Factor A