Treatment of chronic GvHD with mesenchymal stromal cells induces durable responses: A phase II study

Abstract
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 This response was durable, with systemic immunosuppressive therapy withdrawn from two responders, and a further two free from steroids and tapering calcineurin inhibitors.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 naïve T cells and B cells before treatment compared with the nonresponders, and a significantly higher fraction of CD31+ naïve CD4+ T cells. MSC treatment was associated with significant increases in naïve 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 www.ClinicalTrials.gov as #NCT01522716.
Funding Information
  • Karolinska Institutet
  • Tobias Foundation
  • Swedish Society of Medicine
  • Cancerföreningen i Stockholm
  • Stockholms Läns Landsting (20110152)
  • VINNOVA (2010-00501)
  • Swedish Research Council (K2011-??X-20742-04-6)
  • Cancerfonden (11 0315)
  • Karolinska Institutet
  • Svenska Läkaresällskapet
  • Cancerföreningen i Stockholm
  • Stockholms Läns Landsting (20110152)
  • VINNOVA (2010‐00501)
  • Vetenskapsrådet (K2011‐??X‐20742‐04‐6)
  • Cancerfonden (11 0315)