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IL-36γ (IL-1F9) is a biomarker for psoriasis skin lesions.

Authors :
D'Erme AM
Wilsmann-Theis D
Wagenpfeil J
Hölzel M
Ferring-Schmitt S
Sternberg S
Wittmann M
Peters B
Bosio A
Bieber T
Wenzel J
Source :
The Journal of investigative dermatology [J Invest Dermatol] 2015 Apr; Vol. 135 (4), pp. 1025-1032. Date of Electronic Publication: 2014 Dec 19.
Publication Year :
2015

Abstract

In recent years, different genes and proteins have been highlighted as potential biomarkers for psoriasis, one of the most common inflammatory skin diseases worldwide. However, most of these markers are not only psoriasis-specific but also found in other inflammatory disorders. We performed an unsupervised cluster analysis of gene expression profiles in 150 psoriasis patients and other inflammatory skin diseases (atopic dermatitis, lichen planus, contact eczema, and healthy controls). We identified a cluster of IL-17/tumor necrosis factor-α (TNFα)-associated genes specifically expressed in psoriasis, among which IL-36γ was the most outstanding marker. In subsequent immunohistological analyses, IL-36γ was confirmed to be expressed in psoriasis lesions only. IL-36γ peripheral blood serum levels were found to be closely associated with disease activity, and they decreased after anti-TNFα-treatment. Furthermore, IL-36γ immunohistochemistry was found to be a helpful marker in the histological differential diagnosis between psoriasis and eczema in diagnostically challenging cases. These features highlight IL-36γ as a valuable biomarker in psoriasis patients, both for diagnostic purposes and measurement of disease activity during the clinical course. Furthermore, IL-36γ might also provide a future drug target, because of its potential amplifier role in TNFα- and IL-17 pathways in psoriatic skin inflammation.

Details

Language :
English
ISSN :
1523-1747
Volume :
135
Issue :
4
Database :
MEDLINE
Journal :
The Journal of investigative dermatology
Publication Type :
Academic Journal
Accession number :
25525775
Full Text :
https://doi.org/10.1038/jid.2014.532