Fabio D'Amico, Chiara Trovato, Evangelia Skarmoutsou, Giulio A Rossi, Mariagrazia Granata, Valentina Longo, Pietro Gangemi, Maurizio Pettinato, Maria Clorinda Mazzarino
Journal: Journal of dermatological science 2016;80(1):38-44
PMID: 26276441
BACKGROUND
Psoriasis is a chronic inflammatory skin disease. It is characterized by immune cell activation and altered epidermal differentiation. S100A7 (psoriasin) is overexpressed in psoriasis, suggesting a determinant role of this protein in inflammation and keratinocyte differentiation.
OBJECTIVE
The purpose of this study was to investigate the expression of S100A7 in the skin from psoriatic patients undergoing biological therapy with adalimumab, etanercept or ustekinumab.
METHODS
S100A7 expression and distribution were analyzed by immunohistochemistry.
RESULTS
S100A7, overexpressed in epidermal keratinocytes of psoriatic lesions, was downregulated, under the biological therapy with adalimumab, etanercept or ustekinumab, only in patients achieving a PASI score<15.
CONCLUSIONS
Dysregulation of S100A7 may represent a non-negligible player in the maintenance of psoriasis and the relative epidermal changes. Blockage of S100A7 may represent an additional therapeutic approach in the treatment of psoriasis.
Copyright © 2015 Japanese Society for Investigative Dermatology. Published by Elsevier Ireland Ltd. All rights reserved.
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