Teraki Yuichi, Shiohara Tetsuo
Department of Dermatology, Kyorin University School of Medicine, Tokyo, Japan.
Dermatology. 2004;209(1):29-32. doi: 10.1159/000078583.
Fixed drug eruption (FDE) is a distinct type of drug-induced eruption, in which intraepidermal CD8+ T cells in the lesional skin are the final effector cells in the epidermal injury of FDE. Desensitization is a unique approach for the management of drug eruption, which has been reported to be effective in treating FDE. However, the mechanisms underlying desensitization to FDE are quite unknown.
We reported a case of successful desensitization to allopurinol-induced FDE. To clarify the mechanisms underlying desensitization to FDE, we examined the phenotype of T cells in the epidermis of FDE lesions before and after desensitization using flow cytometry.
The overwhelming majority of intraepidermal T cells in the FDE lesion before desensitization consisted of CD8+ T cells, whereas a significant number of CD25+CD4+ T cells were present in the epidermis of FDE lesions after desensitization.
The presence of CD25+CD4+ T cells in the epidermis of FDE lesions may be involved in the induction of desensitization to FDE.
固定性药疹(FDE)是一种独特的药物性皮疹,其中皮损部位的表皮内CD8 + T细胞是FDE表皮损伤的最终效应细胞。脱敏是治疗药疹的一种独特方法,据报道对治疗FDE有效。然而,FDE脱敏的潜在机制尚不清楚。
我们报告了1例成功脱敏治疗别嘌醇诱发的FDE的病例。为阐明FDE脱敏的潜在机制,我们使用流式细胞术检测了脱敏前后FDE皮损表皮中T细胞的表型。
脱敏前FDE皮损中绝大多数表皮内T细胞由CD8 + T细胞组成,而脱敏后FDE皮损表皮中存在大量CD25 + CD4 + T细胞。
FDE皮损表皮中CD25 + CD4 + T细胞的存在可能与FDE脱敏的诱导有关。