Deucravacitinib Improved Interstitial Pneumonia Along with KL-6 Reduction in a Patient with Psoriasis: A Case Report

Yoshihito Mima,1,2 Tsutomu Ohtsuka,2 Norimichi Akiyama,3 Yuta Norimatsu4 1Department of Dermatology, Tokyo Metropolitan Police Hospital, Tokyo, Japan; 2Department of Dermatology, International University of Health and Welfare Hospital, Tochigi, Japan; 3Department of Respiratory Medicine, Fujieda Mun...

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Main Authors: Mima Y, Ohtsuka T, Akiyama N, Norimatsu Y
Format: Article
Language:English
Published: Dove Medical Press 2025-07-01
Series:Clinical, Cosmetic and Investigational Dermatology
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Online Access:https://www.dovepress.com/deucravacitinib-improved-interstitial-pneumonia-along-with-kl-6-reduct-peer-reviewed-fulltext-article-CCID
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Summary:Yoshihito Mima,1,2 Tsutomu Ohtsuka,2 Norimichi Akiyama,3 Yuta Norimatsu4 1Department of Dermatology, Tokyo Metropolitan Police Hospital, Tokyo, Japan; 2Department of Dermatology, International University of Health and Welfare Hospital, Tochigi, Japan; 3Department of Respiratory Medicine, Fujieda Municipal General Hospital, Shizuoka, Japan; 4Department of Dermatology, International University of Health and Welfare Narita Hospital, Chiba, JapanCorrespondence: Yoshihito Mima, Department of Dermatology, Tokyo Metropolitan Police Hospital, 4-22-1 Nakano, Nakano-ku Tokyo, 164-8541, Japan, Tel +81-03-5343-5611, Fax +81-03-5343-5612, Email yoshihito11.mima@gmail.comAbstract: This case report describes a patient with psoriasis and interstitial pneumonia (IP) presenting with linear opacities who was treated with deucravacitinib, aiming to highlight the potential role of deucravacitinib in improving IP. Psoriasis is a chronic immune-mediated skin disease involving T helper (Th) 17 cells, often accompanied by systemic comorbidities. Deucravacitinib, a selective oral tyrosine kinase 2 (TYK2) inhibitor targeting interleukin (IL)-23 and type I interferons, has shown strong efficacy and safety in psoriasis treatment. Interstitial pneumonia (IP) is a group of lung diseases characterized by inflammation, fibrosis, and progressive respiratory decline. Cytokines play key roles in its pathogenesis. Emerging evidence suggests that psoriasis has higher risks of IP, possibly due to shared IL-23/IL-17 pathway. The patient showed marked improvement in skin and lung findings, along with KL-6 levels after deucravacitinib treatment. TYK2 mediates downstream signaling of key pro-fibrotic and pro-inflammatory cytokines involved in IP. Therefore, we consider that deucravacitinib may have contributed to the improvement of IP by blocking these signaling pathways, thereby suppressing chronic T cell–driven inflammation and fibrosis. Further accumulation of cases and continued research will be essential in advancing discussions on the clinical utility of TYK2 inhibitors in IP management.Keywords: interleukin, KL-6, deucravacitinib, T helper cells, tyrosine kinase 2
ISSN:1178-7015