Improvement in Poor Graft Function After Allogeneic Hematopoietic Stem Cell Transplantation Upon Administration of Mesenchymal Stem Cells From Third-Party Donors: A Pilot Prospective Study

被引:65
作者
Liu, Xiaodan [1 ,2 ]
Wu, Meiqing [1 ]
Peng, Yanwen [3 ]
Chen, Xiaoyong [3 ]
Sun, Jing [1 ]
Huang, Fen [1 ]
Fan, Zhiping [1 ]
Zhou, Hongsheng [1 ]
Wu, Xiuli [1 ]
Yu, Guopan [1 ]
Zhang, Xian [1 ]
Li, Yonghua [4 ]
Xiao, Yang [4 ]
Song, Chaoyang [5 ]
Xiang, Andy Peng [3 ]
Liu, Qifa [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Hematol, Guangzhou 510515, Guangdong, Peoples R China
[2] Qingdao Univ, Affiliated Hosp, Dept Hematol, Qingdao 266071, Peoples R China
[3] Sun Yat Sen Univ, Minist Educ, Ctr Stem Cell Biol & Tissue Engn, Key Lab Stem Cells & Tissue Engn, Guangzhou 510275, Guangdong, Peoples R China
[4] Guangzhou Mil Command, Guangzhou Gen Hosp, Dept Hematol, Guangzhou, Guangdong, Peoples R China
[5] Southern Med Univ, Zhujiang Hosp, Dept Hematol, Guangzhou 510515, Guangdong, Peoples R China
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
Poor graft function (PGF); Mesenchymal stem cells (MSCs); Allogeneic hematopoietic stem cell transplantation (allo-HSCT); Third-party donors; EPSTEIN-BARR-VIRUS; INFLUENCING HEMATOLOGICAL RECOVERY; VERSUS-HOST DISEASE; STROMAL CELLS; BONE-MARROW; CYTOMEGALOVIRUS-INFECTIONS; ENHANCE ENGRAFTMENT; COTRANSPLANTATION; RISK; RECURRENCE;
D O I
10.3727/096368912X661319
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Poor graft function (PGF) is a refractory complication that occurs after allogeneic hematopoietic stem cell transplantation (allo-HSCT). In the present study, we prospectively evaluated the efficacy and safety of mesenchymal stem cells (MSCs) expanded from the bone marrow of a third-party donor to patients with PGF after allo-HSCT. Twenty patients with PGF (7 with primary and 13 with secondary PGF) received MSCs (1 x 10(6)/kg) one to three times at 28-day intervals. Seventeen patients were responsive to MSCs, whereas three were not. Within the first 100 days after MSC treatment, 13 patients developed 20 episodes of infection. Moreover, five patients experienced cytomegalovirus-DNA viremia, and seven experienced Epstein-Barr virus (EBV)-DNA viremia within the first 100 days after MSC treatment; three of the latter developed EBV-associated posttransplant lymphoproliferative disorders (PTLD) within the follow-up period. Grade II acute graft-versus-host disease (GVHD) occurred in one patient, and local chronic GVHD occurred in two patients after receiving MSC treatment, including one acute GVHD and one chronic GVHD, respectively, after accepting donor lymphocyte infusions due to PTLD. After a follow-up period of an average of 508 days (range 166-904 days) posttransplantation, 11 patients died. No short-term toxic side effects were observed after MSC treatment. Two patients experienced leukemic relapse. With the exception of three patients with PTLD, no secondary tumors occurred. These results indicate that MSCs derived from the bone marrow of a third-party donor are beneficial in the treatment of both primary and secondary PGF that develops after allo-HSCT. However, additional studies will be needed to determine whether such treatment might increase the risk of EBV infection and reactivation or the development of EBV-associated PTLD.
引用
收藏
页码:1087 / 1098
页数:12
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