4.6 Article

Treatment of chronicGvHDwith mesenchymal stromal cells induces durable responses: A phaseIIstudy

Journal

STEM CELLS TRANSLATIONAL MEDICINE
Volume 9, Issue 10, Pages 1190-1202

Publisher

WILEY
DOI: 10.1002/sctm.20-0099

Keywords

cellular therapy; clinical trials; hematopoietic stem cell transplantation; mesenchymal stem cells; thymus

Funding

  1. Karolinska Institutet
  2. Tobias Foundation
  3. Swedish Society of Medicine
  4. Cancerforeningen i Stockholm
  5. Stockholms Lans Landsting [20110152]
  6. VINNOVA [2010-00501]
  7. Swedish Research Council [K2011-??X-20742-046]
  8. Cancerfonden [11 0315]

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Steroid-refractory chronic graft-vs-host disease (cGvHD) contributes to morbidity after allogeneic hematopoietic stem cell transplantation. Here, we report on 11 patients with severe, refractory cGvHD treated with repeated infusions of allogeneic bone marrow-derived mesenchymal stromal cells (MSC) over a 6- to 12-month period. Six patients responded to MSC treatment following National Institutes of Health response criteria, accompanied by improvement in GvHD-related symptoms and quality of life. This response was durable, with systemic immunosuppressive therapy withdrawn from two responders, and a further two free from steroids and tapering calcineurin inhibitors. All responders displayed a distinct immune phenotype characterized by higher levels of naive T cells and B cells before treatment compared with the nonresponders, and a significantly higher fraction of CD31+ naive CD4+ T cells. MSC treatment was associated with significant increases in naive T cells, B cells, and Tregs 7 days after each infusion. Skin biopsies showed resolution of epidermal pathology. CXCL9 and CXCL10 showed differential responses in responder and nonresponder patients. Our data support the use of MSC infusions as treatment for steroid-refractory cGvHD with durable responses. We propose CXCL9 and CXCL10 as early biomarkers for responsiveness to MSC treatment. Our results highlight the importance of the MSC recipient immune phenotype in promoting treatment response. This trial was registered at as #NCT01522716.

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