Phenotypic Shift during Treatment of Plaque Psoriasis with Ixekizumab.

Q2 Medicine
Caroline Sulich-Moore, David Altman
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引用次数: 0

Abstract

We present a case of a patient with longstanding psoriasis vulgaris who developed an atopic dermatitis-like eruption following long-term IL-17A inhibitor therapy. Following many years of excellent disease control with secukinumab and later ixekizumab, he developed a de novo eczematous eruption, which showed spongiotic dermatitis upon biopsy. The patient was successfully treated for both psoriasis and atopic dermatitis with upadacitinib, a Janus kinase inhibitor. This case suggests an interplay between Th1/Th17 and IL-4/IL-13 immune axes during prolonged biologic therapy, potentially due to upregulation of IL-4 following IL-17 blockade. It highlights the complex immune interactions in inflammatory skin diseases and demonstrates the utility of broader cytokine inhibition in managing evolving presentations.

Ixekizumab治疗斑块型银屑病期间的表型转移。
我们提出了一个病例的患者长期银屑病寻常谁开发一个特应性皮炎样爆发后,长期IL-17A抑制剂治疗。在使用secukinumab和后来的ixekizumab进行多年的良好疾病控制后,他出现了新发湿疹疹,活检显示为海绵状皮炎。患者成功治疗牛皮癣和特应性皮炎与upadacitinib,一种Janus激酶抑制剂。该病例表明,在长期生物治疗期间,Th1/Th17和IL-4/IL-13免疫轴之间存在相互作用,可能是由于IL-17阻断后IL-4的上调。它强调了炎症性皮肤病中复杂的免疫相互作用,并证明了更广泛的细胞因子抑制在管理进化表现中的效用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.60
自引率
0.00%
发文量
104
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