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银屑病患者接受司库奇尤单抗治疗期间原有白癜风的进展

Progression of Pre-Existing Vitiligo during Secukinumab Treatment for Psoriasis.

作者信息

Kim Jin Cheol, Lee Eun-So

机构信息

Department of Dermatology, Ajou University School of Medicine, Suwon, Korea.

出版信息

Ann Dermatol. 2023 May;35(Suppl 1):S117-S121. doi: 10.5021/ad.21.078.

Abstract

Vitiligo has been considered an unexplained paradoxical phenomenon during biologics use. Herein, we report an adult case of progression of pre-existing vitiligo during secukinumab treatment for psoriasis, and we also examined the immunohistochemical changes in relation to biologics use. He was being administered monthly secukinumab of 300 mg dose for 2 years, and all psoriatic lesions were cleared, but pre-existing hypopigmented lesions became more distinct and larger than before unlike when using adalimumab. A skin biopsy of the hypopigmented lesion showed loss of epidermal melanocytes and absence of gp100 immune activities, and he was finally diagnosed with progression of pre-existing vitiligo. Immunohistochemical staining of vitiligo lesion showed decrease in interleukin-17 and tumor necrosis factor-α and increase in CD8+ T cells, interferon-γ, and CXCL10 after the use of secukinumab. In this study, we suggest that biologics-induced cytokine imbalance play a critical role in vitiligo progression in patients with chronic inflammatory diseases, including psoriasis.

摘要

白癜风在使用生物制剂期间一直被视为一种无法解释的矛盾现象。在此,我们报告一例成年患者,在使用司库奇尤单抗治疗银屑病期间,原有白癜风病情进展,并且我们还研究了与使用生物制剂相关的免疫组化变化。他接受每月一次300毫克剂量的司库奇尤单抗治疗2年,所有银屑病皮损均已清除,但原有色素减退性皮损变得比使用阿达木单抗时更明显、更大。对色素减退性皮损进行皮肤活检显示表皮黑素细胞缺失且gp100免疫活性缺乏,最终他被诊断为原有白癜风病情进展。白癜风皮损的免疫组化染色显示,使用司库奇尤单抗后白细胞介素-17和肿瘤坏死因子-α减少,CD8+T细胞、干扰素-γ和CXCL10增加。在本研究中,我们认为生物制剂诱导的细胞因子失衡在包括银屑病在内的慢性炎症性疾病患者的白癜风进展中起关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7f3/10608358/b5bc97f2c58b/ad-35-S117-g001.jpg

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