Charité- Universitätsmedizin Berlin, Department of Dermatology and Allergology, Berlin, Germany.
Allergy. 2010 Sep;65(9):1158-65. doi: 10.1111/j.1398-9995.2010.02341.x. Epub 2010 Mar 10.
The complex pathogenesis of atopic dermatitis (AD) is guided by cell surface receptor-mediated signal transduction regulated in lipid rafts. Miltefosine is a raft-modulating molecule targeting cell membranes. With this controlled clinical study, the clinical and immunomodulatory efficacy of miltefosine was investigated in patients with AD in comparison with a topical corticosteroid treatment.
Sixteen patients with AD were treated topically with miltefosine and hydrocortisone localized on representative AD target lesions for 3 weeks. To assess the clinical efficacy, the three item severity (TIS) score was evaluated before, during and after treatment as well as after 4-week-follow-up period. To study the anti-inflammatory effect of miltefosine on the cellular T cell pattern, skin biopsies were analysed before and after treatment.
The TIS score dropped in both groups significantly after treatment. A carry-over effect was exclusively seen for miltefosine after discontinuing the treatment. These findings were substantiated by thermographic imaging with a significant decrease in the maximum temperature (T(max)) after miltefosine application (P = 0.034, DeltaT(max) = 1.7 degrees C [2.1-3.9]). Immunohistochemically, a reduction in lesional CD4(+)-infiltrating T cells was observed in both treatments. Moreover, increased FoxP3(+) cells were present in the skin after miltefosine treatment (before 5.4% [1.9-9.8], after 6.2% [3.5-9.5]).
We demonstrate that miltefosine is locally active in patients with AD and led to a sustained clinical improvement in local skin inflammation. Moreover, the increased frequency of FoxP3(+) cells in the skin of patients with AD suggests its immunomodulatory properties.
特应性皮炎(AD)的复杂发病机制由细胞表面受体介导的信号转导调控,受脂筏调节。米替福新是一种靶向细胞膜的筏调节分子。通过这项对照临床试验,研究了米替福新在 AD 患者中的临床和免疫调节疗效,并与局部皮质类固醇治疗进行了比较。
16 例 AD 患者局部应用米替福新和氢化可的松治疗代表性 AD 靶皮损,治疗 3 周。为评估临床疗效,在治疗前、治疗中、治疗后及 4 周随访期间评估 TIS 评分。为研究米替福新对细胞 T 细胞模式的抗炎作用,分析治疗前后的皮肤活检。
两组 TIS 评分在治疗后均显著下降。仅在停止治疗后米替福新组出现持续效应。热成像显示,米替福新治疗后最大温度(Tmax)显著降低(P=0.034,DeltaTmax=1.7°C[2.1-3.9]),这一发现得到了证实。免疫组化显示,两种治疗方法均可减少皮损中 CD4+浸润 T 细胞。此外,米替福新治疗后皮肤中 FoxP3+细胞增加(治疗前 5.4%[1.9-9.8],治疗后 6.2%[3.5-9.5])。
我们证明米替福新在 AD 患者中具有局部活性,可持续改善局部皮肤炎症。此外,AD 患者皮肤中 FoxP3+细胞的增加提示其具有免疫调节特性。