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首页> 外文期刊>Cell transplantation >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
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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

机译:异体造血干细胞移植后,第三方供体间充质干细胞给药后移植功能差的改善:一项前瞻性前瞻性研究

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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 × 106/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.
机译:移植物功能不良(PGF)是一种难治性并发症,发生于同种异体造血干细胞移植(allo-HSCT)之后。在本研究中,我们前瞻性评估了异体造血干细胞移植后从第三方供体的骨髓向PGF患者扩增的间充质干细胞(MSC)的疗效和安全性。 20例PGF患者(7例为原发性PGF,13例为继发性PGF),每隔28天接受MSC(1×106 / kg)1-3次。 17名患者对MSC有反应,而3名则没有。在MSC治疗后的前100天内,有13位患者发生了20次感染。此外,在MSC治疗后的前100天内,有5名患者经历了巨细胞病毒-DNA病毒血症,而7名经历了爱泼斯坦-巴尔病毒(EBV)-DNA病毒血症。后者中有3名在随访期内发生了与EBV相关的移植后淋巴组织增生性疾病(PTLD)。接受MSC治疗的两名患者在接受MSC治疗后发生了II级急性移植物抗宿主病(GVHD),局部慢性GVHD发生在两名患者中,包括分别接受了PTLD的供体淋巴细胞输注后的一种急性GVHD和一种慢性GVHD。移植后平均508天(166-904天)的随访期后,有11例患者死亡。 MSC治疗后未观察到短期毒性副作用。两名患者发生白血病复发。除三名PTLD患者外,未发生继发性肿瘤。这些结果表明,来自第三方供体的骨髓间充质干细胞对异基因造血干细胞移植后发生的原发性和继发性PGF均有治疗作用。但是,还需要进行其他研究来确定这种治疗是否会增加EBV感染和再激活的风险,或者是否会增加与EBV相关的PTLD的发生。

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