Type I Pityriasis Rubra Pilaris: Upregulation of Tumor Necrosis Factor α and Response to Adalimumab Therapy

被引:22
作者
Zhang, Yao-Hua
Zhou, Youwen
Ball, Nigel
Su, Ming-Wan
Xu, Jin-Hua
Zheng, Zhi-Zhong
机构
[1] Univ British Columbia, Dept Dermatol, Vancouver, BC V5Z 1M9, Canada
[2] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC V5Z 1M9, Canada
[3] Fudan Univ, Huashan Hosp, Dept Dermatol, Shanghai 200433, Peoples R China
[4] Anhui Med Univ, Dept Dermatol, Hefei, Peoples R China
[5] Univ British Columbia, Dept Skin Sci, Vancouver, BC V5Z 1M9, Canada
关键词
PSORIATIC-ARTHRITIS; INFLIXIMAB; ETANERCEPT; TRIAL;
D O I
10.2310/7750.2010.09023
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Pityriasis rubra pilaris (PAP) has unknown etiology and is often refractory to conventional therapies. Objective: To document a PRP patient's response to adalimumab therapy and to highlight the potential role of tumor necrosis factor (TNF) in the development of PAP skin lesions. Methods: A patient received adalimumab therapy at standard dosing intervals. In addition, the messenger ribonucleic acid (mRNA) of TNF in the lesional and perilesional normal skin was quantified in two patients with PAP. Results: The patient responded to adalimumab therapy and achieved clinical remission by 4 months. There was a significant elevation of TNF mRNA in the lesional skin of PAP. Conclusion: TNF upregulation is detected in PRP lesional skin, consistent with the observed clinical efficacy of TNF blockade for the treatment of PRP.
引用
收藏
页码:185 / 188
页数:4
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