Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/32459
Title: Mesenchymal stromal cells as rescue therapy in biologic-refractory psoriasis: insights from a case series
Authors: Lwin, SM
Solanky, S
Scottà, C
Giacomini, C
Azrielant, S
Tosi, I
Al-Haddabi, A
Duarte-Williamson, E
Dawe, H
Walsh, S
McGrath, JA
Lombardi, G
Dazzi, F
Di Meglio, P
Griffiths, CEM
Keywords: psoriasis;multiple biologic-refractory;mesenchymal stromal cells;immunomodulatory;regulatory T cells;monocytes
Issue Date: 3-Sep-2025
Publisher: Frontiers Media
Citation: Lwin, S.M. et al. (2025) 'Mesenchymal stromal cells as rescue therapy in biologic-refractory psoriasis: insights from a case series', Frontiers in Immunology, 16, 1656724, pp. 1 - 9. doi: 10.3389/fimmu.2025.1656724
Abstract: Cytokine-targeted biologics have revolutionized the management of moderate-to-severe psoriasis; however, all available therapies have failed a growing number of patients. Mesenchymal stromal cells (MSCs), with their immunomodulatory properties, offer a novel therapeutic option. Here, we report the cases of three adult female patients with long-standing, severe plaque psoriasis who were refractory to multiple biologic therapies, and were consequently treated with two intravenous infusions of allogeneic umbilical cord-derived MSCs (UC-MSCs; 1.96 – 3.00 × 10<sup>6</sup> cells/kg) 1 week (W) apart. Two patients received UC-MSCs as monotherapy; one received them alongside etanercept. Upon relapse, two patients resumed their last failed biologic at W9, while one switched to a new biologic at W24. UC-MSCs were well-tolerated and yielded variable clinical benefits. The best responder to MSCs experienced an 87% reduction in the Psoriasis Area and Severity Index (PASI 87) by W4. Two patients showed improved responses to previously failed biologics (absolute PASI of 0–2), sustained for over 2 years following reinitiation. Multi-parameter flow cytometry revealed increased frequencies of CD4<sup>+</sup> and CD8<sup>+</sup> skin-homing (CLA<sup>+</sup>CD103<sup>−</sup>) and skin-recirculating (CLA<sup>+</sup>CD103<sup>+</sup>) memory T cells, CD25<sup>Hi</sup>CD127<sup>Lo</sup>FoxP3<sup>+</sup> regulatory T cells, and non-classical (CD14<sup>Lo</sup>CD16<sup>+</sup>) monocytes, associated with clinical improvements. These findings suggest that UC-MSCs may potentially provide direct benefits for biologic-refractory psoriasis and restore responsiveness to previously ineffective biologics, possibly by resetting the immune response. Further investigation in larger cohorts is warranted.
Description: Data availability statement: The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
Supplementary material: The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2025.1656724/full#supplementary-material
Generative AI statement: The author(s) declare that Generative AI was used in the creation of this manuscript. ChatGPT 4.0 was used to improve the readability of the manuscript. Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.
URI: https://bura.brunel.ac.uk/handle/2438/32459
DOI: https://doi.org/10.3389/fimmu.2025.1656724
Other Identifiers: ORCiD: Cristiano Scottà https://orcid.org/0000-0003-3942-5201
Article number: 1656724
Appears in Collections:Dept of Life Sciences Research Papers

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