Saripalli Yamini V, Gadzia Joseph E, Belsito Donald V
Division of Dermatology, University of Kansas Medical Center, Kansas City 66160-7319, USA.
J Am Acad Dermatol. 2003 Sep;49(3):477-82. doi: 10.1067/s0190-9622(03)01826-7.
Tacrolimus is a macrolactam that prevents the transcription of messenger RNA for various inflammatory cytokines in both helper T cells (types 1 and 2) (T(H)1 and T(H)2). It is currently approved for the treatment of moderate to severe atopic dermatitis, a Th2-mediated disease, in children and adults.
We sought to evaluate the safety and efficacy of tacrolimus ointment 0.1% in the treatment of nickel-induced allergic contact dermatitis, a T(H)1-mediated disease.
This was a double-blind, randomized, vehicle-controlled, bilateral paired comparison study to assess the safety and efficacy of topical tacrolimus (Protopic, Fujisawa Healthcare Inc, Deerfield, Ill) ointment 0.1% in the treatment of allergic contact dermatitis induced by nickel sulfate. Volunteers were individuals with known hypersensitivity to nickel. Reactivity to nickel was graded both as the investigator's global assessment and total signs and symptoms, which consisted of the cumulative grade from 0 to 4 for each of the following parameters: erythema, induration, vesiculation, and pruritus (range of scores: 0-16). Reactivity was assessed in the per-protocol group at 1 and 2 weeks after beginning treatment with study drug and control. Adverse events were assessed in the intent-to-treat population.
Of the 19 volunteers who completed the study (per protocol), 18 had an improvement in total signs and symptoms with tacrolimus versus 10 patients with the vehicle. Of patients, 80% had an improvement in the investigator's global assessment score on the tacrolimus-treated site versus 30% of patients on the placebo-treated site. Overall, tacrolimus was more effective than placebo in ameliorating the nickel reaction. Although the tacrolimus treated site was clear or almost clear in a greater number of individuals at week 1, this difference did not become significant until the second week of the study. Other than application site burning in 25% of volunteers, no significant adverse events were noted in the intent-to-treat population.
Topical tacrolimus (Protopic, Fujisawa Healthcare Inc) ointment 0.1% may be an option for the treatment of allergic contact dermatitis induced by nickel.
他克莫司是一种大环内酯类药物,可阻止辅助性T细胞(1型和2型)(T(H)1和T(H)2)中各种炎性细胞因子的信使核糖核酸转录。它目前已被批准用于治疗儿童和成人的中度至重度特应性皮炎,这是一种由Th2介导的疾病。
我们试图评估0.1%他克莫司软膏治疗镍诱导的过敏性接触性皮炎(一种由T(H)1介导的疾病)的安全性和有效性。
这是一项双盲、随机、赋形剂对照、双侧配对比较研究,旨在评估局部应用0.1%他克莫司软膏(普特彼,藤泽医疗保健公司,伊利诺伊州迪尔菲尔德)治疗硫酸镍诱导的过敏性接触性皮炎的安全性和有效性。志愿者为已知对镍过敏的个体。对镍的反应性通过研究者整体评估和总体征及症状进行分级,总体征及症状由以下各项参数的累积分级组成:红斑、硬结、水疱形成和瘙痒(评分范围:0至16)。在按方案治疗组中,在开始使用研究药物和对照治疗1周和2周后评估反应性。在意向性治疗人群中评估不良事件。
在完成研究的19名志愿者(按方案)中,18名使用他克莫司的患者总体征及症状有所改善,而使用赋形剂的患者有10名。在患者中,80%使用他克莫司治疗部位的研究者整体评估评分有所改善,而安慰剂治疗部位的患者为30%。总体而言,他克莫司在改善镍反应方面比安慰剂更有效。虽然在第1周时,使用他克莫司治疗的部位在更多个体中变得清晰或几乎清晰,但这种差异直到研究的第二周才变得显著。在意向性治疗人群中,除了25%的志愿者出现用药部位烧灼感外,未观察到显著的不良事件。
0.1%局部用他克莫司软膏(普特彼,藤泽医疗保健公司)可能是治疗镍诱导的过敏性接触性皮炎的一种选择。