Volume 175, Issue 6 pp. 1243-1250
Translational Research

Impact of systemic alitretinoin treatment on skin barrier gene and protein expression in patients with chronic hand eczema

V. Kumari

V. Kumari

Department of Dermatology and Allergy, Allergy-Center-Charité, Charité – Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, Germany

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K. Timm

K. Timm

Department of Dermatology and Allergy, Allergy-Center-Charité, Charité – Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, Germany

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A.A. Kühl

A.A. Kühl

Department of Gastroenterology, Infection and Rheumatology/Research Centre ImmunoSciences (RCIS), Charité-Campus Benjamin Franklin, Charité – Universitätsmedizin, Berlin, Germany

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G. Heine

G. Heine

Department of Dermatology and Allergy, Allergy-Center-Charité, Charité – Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, Germany

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M. Worm

Corresponding Author

M. Worm

Department of Dermatology and Allergy, Allergy-Center-Charité, Charité – Universitätsmedizin Berlin, Charitéplatz 1, 10117 Berlin, Germany

Correspondence

Margitta Worm.

E-mail: [email protected]

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First published: 02 August 2016
Citations: 24
Funding sources This work was supported by a grant from Deutsche Forschungsgemeinschaft to Margitta Worm and Guido Heine (TRR130).
Conflicts of interest The authors state no conflicts of interest.
§
V.K. and K.T. contributed equally and share authorship.

Plain language summary available online

Summary

Background

Chronic hand eczema (CHE) is a common inflammatory skin disease that affects approximately 10% of the population. Systemic alitretinoin has been shown to be effective in patients with CHE who are refractory to topical corticosteroids.

Objectives

To analyse the impact of alitretinoin on the skin barrier genes and protein expression in the skin lesions of patients with CHE.

Materials and methods

Fifteen patients with CHE were treated with 30 mg daily of alitretinoin for up to 27 weeks. Disease severity was assessed using a clinical score. Skin biopsies from all the patients were evaluated before and after therapy for the expression of Ki-67, various skin barrier genes and thymic stromal lymphopoietin (TSLP) by real-time quantitative polymerase chain reaction and immunohistochemistry.

Results

After alitretinoin application, an improvement in the clinical severity of CHE was observed in the majority of patients. Analysis of skin biopsies before treatment showed a significant increase in Ki-67-positive cells in the suprabasal layer and a dysregulated expression of various skin barrier genes, such as claudin 1, loricrin, filaggrin and cytokeratin 10, which were normalized after treatment. TSLP was significantly upregulated in patients with CHE and also normalized after alitretinoin treatment and negatively correlated with filaggrin.

Conclusions

Our data indicate that the expression of barrier genes and proteins was normalized following treatment with alitretinoin in patients with CHE. The change in expression levels of these genes correlated with the clinical efficacy, suggesting that alitretinoin exhibits a disease-modifying activity. TSLP is upregulated in CHE and seems to counteract filaggrin expression in the skin.

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