已发表论文

斯佩索利单抗治疗泛发性脓疱型银屑病:IL-36RN 突变及合并斑块状银屑病的影响

 

Authors Li W, Liang J, Luo Y, Chen S, Xia M, Ye H , Yang B, Luo Q

Received 17 April 2025

Accepted for publication 17 July 2025

Published 9 August 2025 Volume 2025:18 Pages 1931—1935

DOI https://doi.org/10.2147/CCID.S533564

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 3

Editor who approved publication: Dr Michela Starace

Wei Li,1– 3,* Jingyao Liang,2,* Yuwu Luo,2 Shuting Chen,2 Manqi Xia,2 Hui Ye,2 Bin Yang,1,3 Quan Luo2 

1Department of Dermatology, First Affiliated Hospital of Jinan University, Guangzhou, 510630, People’s Republic of China; 2Department of Dermatology, Guangzhou Dermatology Hospital, Guangzhou, 510095, People’s Republic of China; 3Department of Dermatology, Dermatology Hospital of Southern Medical University, Guangzhou, People’s Republic of China

*These authors contributed equally to this work

Correspondence: Bin Yang, Email yangbin1@smu.edu.cn Quan Luo, Email luoquan666@126.com

Abstract: We present a case series involving five patients with generalized pustular psoriasis (GPP) who received a single intravenous dose of 900 mg spesolimab in our department from September 2023 to January 2024. Spesolimab was effective in three patients, regardless of their IL-36RN gene mutation status. Two patients with concomitant plaque psoriasis, despite initially poor responses to spesolimab, achieved resolution of pustules after switching their therapy to ixekizumab or secukinumab. This study highlights the potential of spesolimab in managing GPP, especially in genetically distinct groups, and emphasizes the importance of tailored therapeutic approaches. These findings suggest that spesolimab can effectively treat GPP, regardless of IL-36RN gene mutation status. However, its therapeutic efficacy may be suboptimal in patients with concomitant plaque psoriasis, indicating the need for further investigation to optimize treatment outcomes in this subgroup.

Keywords: spesolimab, generalized pustular psoriasis, IL-36RN mutations