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生物疗法(肿瘤坏死因子-α拮抗剂)诱发的银屑病:肿瘤坏死因子-α与干扰素-α之间的细胞因子失衡?

Biologic therapy (TNF-alpha antagonists)-induced psoriasis: a cytokine imbalance between TNF-alpha and IFN-alpha?

作者信息

Cuchacovich Raquel, Espinoza Carmen G, Virk Zia, Espinoza Luis R

机构信息

Section of Rheumatology, Departments of Internal Medicine and Pathology, LSU Health Sciences Center at New Orleans, New Orleans, LA 70115, USA.

出版信息

J Clin Rheumatol. 2008 Dec;14(6):353-6. doi: 10.1097/RHU.0b013e318190dd88.

DOI:10.1097/RHU.0b013e318190dd88
PMID:19033869
Abstract

We report 3 patients with psoriatic arthritis and 2 with rheumatoid arthritis who developed worsening, and/or de novo psoriasis, and/or psoriasiform rash, while on tumor necrosis factor antagonist therapy. All 5 patients initially presented with active skin, and/or joint inflammatory involvement, and exhibited significant clinical response to tumor necrosis factor antagonist therapy. Within approximately 6 months, however, psoriatic and/or psoriasiform rash developed de novo in 2 rheumatoid arthritis patient and exacerbated in the other 3 patients. Biopsy findings revealed histologic and immunohistochemical changes indistinguishable from psoriasis.Psoriatic rash improved after discontinuation of biologic therapy and/or initiation of a short course of oral prednisone. One patient with psoriatic arthritis was rechallenged with infliximab due to exacerbation of both psoriasis and psoriatic arthritis, and this was followed by prompt improvement of both conditions. At 6 months follow-up, this patient remains under excellent control. To date, there have been over 50 cases of this type of dermatologic complication described. Interferon alpha seems to play an important role in the pathogenesis of this complication. This type of complication has been described with all 3 available tumor necrosis factor inhibitors, and most patients improve after discontinuation of biologic therapy.

摘要

我们报告了3例银屑病关节炎患者和2例类风湿关节炎患者,他们在接受肿瘤坏死因子拮抗剂治疗期间出现病情恶化,和/或新发银屑病,和/或银屑病样皮疹。所有5例患者最初均表现为皮肤和/或关节的活动性炎症受累,并且对肿瘤坏死因子拮抗剂治疗表现出显著的临床反应。然而,在大约6个月内,2例类风湿关节炎患者新发了银屑病和/或银屑病样皮疹,另外3例患者病情加重。活检结果显示组织学和免疫组化变化与银屑病难以区分。停用生物治疗和/或开始短期口服泼尼松后,银屑病皮疹有所改善。1例银屑病关节炎患者因银屑病和银屑病关节炎病情加重而再次接受英夫利昔单抗治疗,随后两种病情均迅速改善。在6个月的随访中,该患者病情仍得到良好控制。迄今为止,已描述了50多例这种类型的皮肤并发症。干扰素α似乎在这种并发症的发病机制中起重要作用。所有3种可用的肿瘤坏死因子抑制剂都出现过这种类型的并发症,大多数患者在停用生物治疗后病情改善。

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