Cutaneous autoimmune blistering disease during mirikizumab therapy in a patient with ulcerative colitis: a new potential trigger?

Autoimmune blistering diseases (AIBDs) may occur as adverse effects of various therapies, including biologics. Data on their association with IL-23 inhibitors in ulcerative colitis (UC) remain limited. We report the case of a 59-year-old man with UC who developed pruritic cutaneous bullae emerging within days following mirikizumab infusion. Histopathological examination and direct immunofluorescence demonstrated findings consistent with an AIBD. Following the withdrawal of mirikizumab, the residual cutaneous lesions progressively improved under corticosteroid therapy, suggesting a temporal association with the biologic exposure. This case highlights that mirikizumab may represent a potential trigger of an AIBD in susceptible individuals with UC. Clinicians should be aware of this rare but relevant complication to ensure timely recognition and management.

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Publication Details

Journal
Journal of Crohn s and Colitis
Published
2026-02-01
DOI
https://doi.org/10.1093/ecco-jcc/jjaf235
Citations
1
Primary Topic
Autoimmune Bullous Skin Diseases
Type
article
Field-Weighted Citation Impact
36.00
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article

Cutaneous autoimmune blistering disease during mirikizumab therapy in a patient with ulcerative colitis: a new potential trigger?

Lucia Centanni, Fabrizio Fanizzi, Ferdinando D’amico, Silvio Danese
1 citations
Journal of Crohn s and Colitis
Autoimmune Bullous Skin Diseases
36.00
article

Cutaneous autoimmune blistering disease during mirikizumab therapy in a patient with ulcerative colitis: a new potential trigger?

Lucia Centanni, Fabrizio Fanizzi, Ferdinando D’amico, Silvio Danese
article en
1 citations

Abstract

Autoimmune blistering diseases (AIBDs) may occur as adverse effects of various therapies, including biologics. Data on their association with IL-23 inhibitors in ulcerative colitis (UC) remain limited. We report the case of a 59-year-old man with UC who developed pruritic cutaneous bullae emerging within days following mirikizumab infusion. Histopathological examination and direct immunofluorescence demonstrated findings consistent with an AIBD. Following the withdrawal of mirikizumab, the residual cutaneous lesions progressively improved under corticosteroid therapy, suggesting a temporal association with the biologic exposure. This case highlights that mirikizumab may represent a potential trigger of an AIBD in susceptible individuals with UC. Clinicians should be aware of this rare but relevant complication to ensure timely recognition and management.

Journal of Crohn s and ColitisVol. 20(2)
Vita-Salute San Raffaele University (IT), IRCCS Ospedale San Raffaele (IT)
Good health and well-being
Openalex Percentile: Top 1%
Autoimmune Bullous Skin Diseases
36.00
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Cutaneous autoimmune blistering disease during mirikizumab therapy in a patient with ulcerative colitis: a new potential trigger? — Lucia Centanni, Fabrizio Fanizzi, et al. · Journal of Crohn s and Colitis (2026) | TGRS Research Map | TGRS