Efficacy of Bone Marrow-Derived Mesenchymal Stem Cells in the Treatment of Sclerodermatous Chronic Graft-versus-Host Disease: Clinical Report

被引:142
作者
Zhou, Hong [1 ,2 ,3 ]
Guo, Mei [4 ]
Bian, Chunjing [1 ,2 ,3 ]
Sun, Zhao [1 ,2 ,3 ]
Yang, Zhuo [1 ,2 ,3 ]
Zeng, Yang [1 ,2 ,3 ]
Ai, HuiSheng [4 ]
Zhao, Robert Chunhua [1 ,2 ,3 ]
机构
[1] Chinese Acad Med Sci, Inst Basic Med Sci, Ctr Excellence Tissue Engn, Beijing 100005, Peoples R China
[2] Chinese Acad Med Sci, Sch Basic Med, Ctr Excellence Tissue Engn, Beijing 100005, Peoples R China
[3] Peking Union Med Coll, Beijing 100005, Peoples R China
[4] Acad Mil Med Sci, Affiliated Hosp, Dept Hematol & Transplantat, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Bone marrow-derived mesenchymal stem cell; Chronic graft-versus-host disease; Sclerodermatous chronic graft-versus-host disease; Allogeneic hematopoietic cell transplantation; CHRONIC GVHD; HIGH-RISK; IN-VITRO; COTRANSPLANTATION; DIFFERENTIATION; FEASIBILITY; LYMPHOCYTE; INFUSION; CRITERIA; THERAPY;
D O I
10.1016/j.bbmt.2009.11.006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The success of treatment for sclerodermatous chronic graft-versus-host disease (ScGVHD) remains disappointing. The immunomodulatory ability of bone marrow (BM) derived mesenchymal stem cells (MSCs) shows promise in treating GVHD, especially given its previous success in treating patients with acute GVHD (aGVHD). The potential efficacy and safety issues for treating cGVHD, particularly ScGVHD, remain to be clarified, however. Here, we report 4 patients with ScGVHD who received MSCs expanded ex vivo from unrelated donors by intra-BM injection. After MSC infusion, the ratio of helper T lymphocyte (Th) 1 cells to Th2 cells was dramatically reversed, with an increase in Th 1 and a decrease in Th2 achieving a new balance. Correspondingly, symptoms gradually improved in all 4 patients. During the course of MSC treatment, the patients' vital signs and laboratory results remained normal. At the time of this report, none of the 4 patients had experienced recurrence of leukemia. Although this study alone cannot guarantee the application of MSCs in ScGVHD, our findings strongly suggest that this treatment is therapeutically practicable, with no detectable side effects. This approach may provide new insight into the clinical treatment of ScGVHD, with the aim of greatly increasing the survival rate in patients with leukemia who undergo allogeneic BM transplantation (BMT). Biol Blood Marrow Transplant 16: 403-412 (2010) (C) 2010 American Society fir Blood and Marrow Transplantation
引用
收藏
页码:403 / 412
页数:10
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