Kinetics and differential expression of the skin-related chemokines CCL27 and CCL17 in psoriasis, atopic dermatitis and allergic contact dermatitis

被引:58
作者
Riis, Jette L. [1 ]
Johansen, Claus [1 ]
Vestergaard, Christian [1 ]
Bech, Rikke [1 ]
Kragballe, Knud [1 ]
Iversen, Lars [1 ]
机构
[1] Aarhus Sygehus, Dept Dermatol, DK-8000 Aarhus, Denmark
关键词
CCL27; CCL17; CCR10; CCR4; inflammatory skin diseases; T-CELLS; TOPICAL APPLICATION; RECEPTOR CCR4; IN-VITRO; INFLAMMATION; ELICITATION; RECRUITMENT; PATHOGENESIS; TRAFFICKING; OXAZOLONE;
D O I
10.1111/j.1600-0625.2011.01323.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
CCL27 and CCL17 are chemokines believed to be involved in the process of establishing the inflammatory infiltrate, characteristic for the various inflammatory skin diseases. The skin-specific CCL27 binds the chemokine receptor-10 (CCR10), and CCL17 is a chemokine receptor-4 (CCR4) ligand. The purpose of our study was to characterize the expression of CCL27 and CCL17 in the inflammatory skin diseases: psoriasis, atopic dermatitis (AD) and acute allergic contact dermatitis (ACD) induced in nickel-sensitive individuals. Surprisingly, our studies revealed a markedly decreased CCL27 mRNA and protein expression in psoriatic lesions compared with non-lesional psoriatic skin. A minor CCL17 mRNA increase was measured in lesional psoriatic skin. No alterations were found in AD. In ACD, we found a pronounced (90-fold) raise in CCL17 mRNA and a 50-fold increase in CCL17 protein compared with normal skin. A kinetic ACD study of CCL17 expression showed the highest mean value 24 h after hapten application. Furthermore, we found the mRNA levels of CCR10 and CCR4 paralleling the results of their corresponding ligands. Overall, our principal findings were a distinct decrease in CCL27 in lesional psoriatic skin and a marked upregulation of CCL17 in ACD. These findings underscore the differential cutaneous T-cell recruitment in different inflammatory diseases.
引用
收藏
页码:789 / 794
页数:6
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