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

Institutions

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
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Mesenchymal stromal cells as rescue therapy in biologic-refractory psoriasis: insights from a case series

Shir Azrielant, Sarah Walsh, Chiara Giacomini, Su M. Lwin et al.
Frontiers in Immunology
Mesenchymal stem cell research
article

Mesenchymal stromal cells as rescue therapy in biologic-refractory psoriasis: insights from a case series

Shir Azrielant, Sarah Walsh, Chiara Giacomini, Su M. Lwin, Francesco Dazzi, Cristiano Scottà, Christopher E.M. Griffiths, Isabella Tosi, Shane Solanky, Hannah Dawe, John A. McGrath, Giovanna Lombardi, Paola Di Meglio, Atheer Al-Haddabi, Emelia Duarte-Williamson
article en

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 <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.

Frontiers in ImmunologyVol. 16
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)
Openalex Percentile: Top 68%
Mesenchymal stem cell research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.