ORIGINAL RESEARCH article
Front. Immunol.
Sec. Inflammation
Volume 16 - 2025 | doi: 10.3389/fimmu.2025.1648830
A murine model of prurigo nodularis-like skin lesions induced by persistent scratching under type 2 inflammatory conditions
Provisionally accepted- 1Shenzhen Hospital, Peking University, Shenzhen, China
- 2Shenzhen Peking University-The Hong Kong University of Science and Technology Medical Center, Shenzhen, China
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Introduction:Prurigo nodularis (PN) is a chronic inflammatory dermatosis characterized by robust pruritus and highly keratinizing nodules sympathetically distributed on the trunk and extensor sides of the limbs with an impact on quality of life and socioeconomic burden. To investigate the pathogenesis and develop novel therapeutic approaches, a preclinical animal model recapitulating the PN phenotypes is needed. Methods:We constructed a novel PN-like mouse model by applying repetitive mechanical scratching in the context of type 2 inflammation. We utilized 6-8-week-old C57BL/6 mice for a 28 - day modeling study. The modeling protocol consisted of daily MC903 treatment plus 100 cell scraper scratches for the first 14 days, followed by alternate-day MC903 with continued daily scratching for the subsequent 14 days, with bandaging applied to prevent spontaneous scratching. Results: Histological analysis of lesions revealed aberrant epidermal hyperplasia and differentiation, dermal fibrosis, inflammatory infiltration, angiogenesis, increased intraepidermal nerve fiber density, and enhanced nerve fiber sprouting. Immunological characterization revealed a mixed Th1/Th2/Th17/Th22 profile with a skewing toward Th17/Th22 polarization. Conclusion: This optimized model faithfully recapitulates the key clinicopathological features of PN patients, providing a robust preclinical platform for investigating disease mechanisms and evaluating potential therapeutics.
Keywords: prurigo nodularis, preclinical model, type 2 inflammation, Th17/Th22 skewing, Dermal fibrosis
Received: 17 Jun 2025; Accepted: 13 Oct 2025.
Copyright: © 2025 Wu, Li, Huang, Tang, Zhang, Yan, Chen and Dou. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Xiaofan Chen, littlecanva@163.com
Xia Dou, drdouxia@163.com
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