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Updated: Feb 15, 2026

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在患有性结肠炎的患者治疗mirikizumab期间,皮肤自身免疫性水泡性疾病:一种新的潜在触发因素?
Lucia Centanni1,2, Fabrizio Fanizzi1,2, Ferdinando D'amico1
1Gastroenterology and Endoscopy, IRCCS San Raffaele Hospital, Milan, Italy.
Journal of Crohn's & colitis
|February 14, 2026
概括
像mirikizumab这样的IN-23 (IL-23) 抑制剂很少会在性结肠炎 (UC) 患者中引发自身免疫性水泡性疾病 (AIBD). 对于易受感染的个体来说,迅速识别和管理至关重要.
科学领域:
- 皮肤病学 皮肤病学
- 胃肠病学 胃肠病学
- 免疫学 免疫学 免疫学
背景情况:
- 自身免疫性水泡性疾病 (AIBD) 是众所周知的各种疗法的不良影响,包括生物药物.
- 在性结肠炎 (UC) 患者中,IL-23抑制剂和AIBD之间的关联存在有限的数据.
研究的目的:
- 报告患有UC的患者在mirikizumab治疗后发生的AIBD病例.
- 要突出IL-23抑制剂触发AIBDs的潜力.
主要方法:
- 一个59岁的男性UC患者的病例报告.
- 在mirikizumab输注后,皮肤上出现的皮球的临床观察.
- 组织病理学检查和直接免疫光检查.
- 评估对mirikizumab停用和皮质类固醇治疗的反应.
主要成果:
- 患者在mirikizumab输注后的几天内出现了AIBD症状.
- 组织病理学和免疫光学证实了AIBD.
- 病变在mirikizumab停止和皮质类固醇治疗后得到改善,这表明存在联系.
结论:
- 在易受UC患者中,Mirikizumab可能是AIBD的潜在触发因素.
- 临床医生应该对这种罕见的并发症保持警.
- 及时识别和管理至关重要.
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