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

被引:55
作者
Boberg, Erik [1 ,2 ]
von Bahr, Lena [1 ]
Afram, Gabriel [2 ,3 ]
Lindstrom, Carina [4 ]
Ljungman, Per [3 ,4 ]
Heldring, Nina [1 ]
Petzelbauer, Peter [5 ]
Legert, Karin Garming [6 ]
Kadri, Nadir [1 ]
Le Blanc, Katarina [1 ,4 ]
机构
[1] Karolinska Inst, Dept Lab Med, Stockholm, Sweden
[2] Karolinska Univ Hosp, Dept Hematol, Stockholm, Sweden
[3] Karolinska Inst, Dept Med, Stockholm, Sweden
[4] Karolinska Univ Hosp Huddinge, Dept Cellular Therapy & Allogene Stem Cell Transp, Stockholm, Sweden
[5] Med Univ Vienna, Dept Dermatol, Skin & Endothelial Res Div, Vienna, Austria
[6] Karolinska Inst, Dept Dent Med, Stockholm, Sweden
基金
瑞典研究理事会;
关键词
cellular therapy; clinical trials; hematopoietic stem cell transplantation; mesenchymal stem cells; thymus; VERSUS-HOST-DISEASE; CONSENSUS DEVELOPMENT PROJECT; REGULATORY T-CELLS; STEM-CELLS; CLINICAL-TRIALS; EXTRACORPOREAL PHOTOPHERESIS; CRITERIA; HEALTH; RECOVERY; TRANSPLANTATION;
D O I
10.1002/sctm.20-0099
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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 This response was durable, with systemic immunosuppressive therapy withdrawn from two responders, and a further two free from steroids and tapering calcineurin inhibitors.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.
引用
收藏
页码:1190 / 1202
页数:13
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