Shao Xinyi, Chen Tingqiao, Pan Xingyu, Chen Shuang, Chen Yangmei, Chen Jin
Department of Dermatology, the First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Front Immunol. 2024 Dec 17;15:1455050. doi: 10.3389/fimmu.2024.1455050. eCollection 2024.
Biological drugs are extensively used to treat various inflammatory diseases, including psoriasis, atopic dermatitis (AD), and rheumatoid arthritis. While generally effective and safe, these therapies have been increasingly associated with secondary development of vitiligo, especially with anti-TNF α and anti-IL17 drugs. Dupilumab, an IL-4 receptor alpha antagonist used in moderate to severe AD, rarely induces vitiligo. This study reports two cases of new-onset vitiligo following dupilumab treatment for AD. The first case involves an 80-year-old male who developed vitiligo patches appeared on the chest, back, and lower limbs after 2 months of dupilumab therapy. Despite discontinuation of dupilumab, the vitiligo did not regress. The second case describes a 14-year-old female who experienced depigmentation on her forehead one month into dupilumab treatment, with partial improvement of vitiligo lesions over time despite continued therapy. This phenomenon may be due to dupilumab blocking type 2 inflammation, disrupting normal skin homeostasis, and exacerbating type 1 inflammation. These cases, supplemented with a literature review, highlight the potential for biologic drug-induced vitiligo and underscore the need for awareness of such adverse events in clinical practice. The mechanisms underlying this phenomenon likely involve disruption of the Th1/Th2/Th17 cytokine balance, suggesting that targeted therapies may inadvertently exacerbate type 1 inflammation, leading to vitiligo. With the rising use of biologics, clinicians should carefully consider the risk of vitiligo when prescribing these treatments.
生物药物被广泛用于治疗各种炎症性疾病,包括银屑病、特应性皮炎(AD)和类风湿性关节炎。虽然这些疗法总体上有效且安全,但它们与白癜风的继发发展越来越相关,尤其是与抗TNFα和抗IL17药物。度普利尤单抗是一种用于中重度AD的IL-4受体α拮抗剂,很少诱发白癜风。本研究报告了两例度普利尤单抗治疗AD后新发白癜风的病例。第一例涉及一名80岁男性,在度普利尤单抗治疗2个月后,胸部、背部和下肢出现白癜风斑块。尽管停用了度普利尤单抗,但白癜风并未消退。第二例描述了一名14岁女性,在度普利尤单抗治疗1个月后前额出现色素脱失,尽管继续治疗,白癜风皮损随时间部分改善。这种现象可能是由于度普利尤单抗阻断2型炎症,破坏正常皮肤稳态,并加剧1型炎症。这些病例结合文献综述,突出了生物药物诱发白癜风的可能性,并强调在临床实践中需要认识到此类不良事件。这种现象的潜在机制可能涉及Th1/Th2/Th17细胞因子平衡的破坏,这表明靶向治疗可能会无意中加剧1型炎症,导致白癜风。随着生物制剂使用的增加,临床医生在开这些治疗药物时应仔细考虑白癜风的风险。