Involvement of CCL27-CCR10 interactions in drug-induced cutaneous reactions - 25/08/11

Madrid and Málaga, Spain
Abstract |
Background |
Drug-induced skin reactions, including toxic epidermal necrolysis and Stevens-Johnson syndrome, are severe bullous cutaneous diseases of uncertain etiology, although cytotoxic T cells seem to be involved. Cutaneous T cell–attracting chemokine (CTACK/CCL27) is selectively expressed in skin and attracts CCR10-expressing cells. Exclusive CTACK expression by keratinocytes suggests its involvement in inflammatory skin diseases.
Objective |
We addressed whether CTACK/CCL27 production by the epidermis and CCR10+ lymphocytes are involved in toxic epidermal necrolysis and Stevens-Johnson syndrome.
Methods |
We measured CTACK expression by epidermal cells in 2 patients with drug-induced bullous skin reactions and compared it to lesional skin from several drug-induced exanthemas. In parallel we measured CCR10 mRNA in peripheral blood mononuclear cells from the patients during the course of the disease and in lymphocytes infiltrating the skin.
Results |
CTACK expression levels in skin biopsies from the 2 patients with drug-induced bullous reactions were higher than those found in healthy subjects or in other drug-induced exanthemas. CCR10 mRNA levels were also elevated in peripheral blood lymphocytes and in lesional skin during the acute phase of the disease. Moreover, resolution was associated with a return to baseline of both CTACK and CCR10 receptor expression.
Conclusion |
CTACK-CCR10 interactions may be involved in the selective recruitment to the skin of cytotoxic lymphocytes in toxic epidermal necrolysis and Stevens-Johnson syndrome, as well as in less severe drug-induced cutaneous diseases.
Le texte complet de cet article est disponible en PDF.Keywords : Stevens-Johnson syndrome, toxic epidermal necrolysis, drug allergy, chemokine, CTACK, CCL27, CCR10, exanthema
Abbreviations : CLA, CTACK, GPR-2, ILC, PBMC, PCR, RT-PCR, SJS, TEN, TNF
Plan
| This work was supported by grants FIS PI02/1027, FIS 01401, and CAM 08.3/0020/20031. |
Vol 114 - N° 2
P. 335-340 - août 2004 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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