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CCL27-CCR10相互作用在药物性皮肤反应中的作用

Involvement of CCL27-CCR10 interactions in drug-induced cutaneous reactions.

作者信息

Tapia Beatriz, Padial Antonia, Sánchez-Sabaté Elena, Alvarez-Ferreira Javier, Morel Esther, Blanca Miguel, Bellón Teresa

机构信息

Research Unit, Hospital Universitario La Paz, Hospital Carlos Haya, Madrid, Spain.

出版信息

J Allergy Clin Immunol. 2004 Aug;114(2):335-40. doi: 10.1016/j.jaci.2004.04.034.

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.

摘要

背景

药物性皮肤反应,包括中毒性表皮坏死松解症和史蒂文斯-约翰逊综合征,是病因不明的严重大疱性皮肤病,尽管细胞毒性T细胞似乎参与其中。皮肤T细胞趋化因子(CTACK/CCL27)在皮肤中选择性表达,并吸引表达CCR10的细胞。角质形成细胞特异性表达CTACK表明其参与炎症性皮肤病。

目的

我们探讨表皮产生的CTACK/CCL27和CCR10+淋巴细胞是否参与中毒性表皮坏死松解症和史蒂文斯-约翰逊综合征。

方法

我们检测了2例药物性大疱性皮肤反应患者表皮细胞的CTACK表达,并将其与几种药物性皮疹的皮损进行比较。同时,我们检测了疾病过程中患者外周血单核细胞以及浸润皮肤的淋巴细胞中的CCR10 mRNA。

结果

2例药物性大疱性反应患者皮肤活检中的CTACK表达水平高于健康受试者或其他药物性皮疹。在疾病急性期,外周血淋巴细胞和皮损中的CCR10 mRNA水平也升高。此外,病情缓解与CTACK和CCR10受体表达恢复至基线相关。

结论

CTACK-CCR10相互作用可能参与中毒性表皮坏死松解症和史蒂文斯-约翰逊综合征中细胞毒性淋巴细胞向皮肤的选择性募集,以及不太严重的药物性皮肤病。

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