Mesenchymal stromal cells as rescue therapy in biologic-refractory psoriasis: insights from a case series
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 <b><sup>-</sup></b> ) 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.
Authors
- Shir Azrielant (ORCID: https://orcid.org/0000-0002-1094-7113)
- Sarah Walsh (ORCID: https://orcid.org/0000-0002-8279-0506)
- Chiara Giacomini
- Su M. Lwin (ORCID: https://orcid.org/0000-0002-3325-3675)
- Francesco Dazzi (ORCID: https://orcid.org/0000-0003-2407-236X)
- Cristiano Scottà (ORCID: https://orcid.org/0000-0003-3942-5201)
- Christopher E.M. Griffiths (ORCID: https://orcid.org/0000-0001-5371-4427)
- Isabella Tosi (ORCID: https://orcid.org/0000-0002-2638-8539)
- Shane Solanky
- Hannah Dawe
- John A. McGrath (ORCID: https://orcid.org/0000-0002-3708-9964)
- Giovanna Lombardi (ORCID: https://orcid.org/0000-0003-4496-3215)
- Paola Di Meglio
- Atheer Al-Haddabi
- Emelia Duarte-Williamson
Institutions
- King's College London (GB)
- Guy's and St Thomas' NHS Foundation Trust (GB)
- Tel Aviv Sourasky Medical Center (IL)
- Kings Health Partners (GB)
- King's College School (GB)
- King's College Hospital (GB)
- Brunel University of London (GB)
Publication Details
- Journal
- Frontiers in Immunology
- Published
- 2025-09-03
- DOI
- https://doi.org/10.3389/fimmu.2025.1656724
- Primary Topic
- Mesenchymal stem cell research
- Type
- article
- Field-Weighted Citation Impact
- 0.00