Department of Hematology, First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu Province, China.
Int J Lab Hematol. 2010 Apr;32(2):256-64. doi: 10.1111/j.1751-553X.2009.01181.x. Epub 2009 Jul 28.
Mesenchymal stem cells (MSCs) may be employed to support hematopoietic reconstitution and mitigate graft-vs.-host disease (GVHD) in transplantation of hematopoietic stem cells (HSCs). The aim of this study was to explore the feasibility and safety of cotransplantation culture-expanded MSCs and HSCs from the same human leukocyte antigen (HLA)-identical sibling donor in Chinese patients with hematologic diseases. Bone marrow mononuclear cells from healthy donors were cultured and expanded ex vivo. Immunophenotype, adipogenic and osteogenic differentiation potential, and karyotype of the harvested MSCs were detected on those who had been cotransplanted with HSCs and MSCs from the same donor. Hematopoietic reconstitutions, complications, and clinical outcomes were observed after cotransplantation in these patients. (1.77 +/- 0.40) x 10(6)/kg (donor's weight) MSCs were successfully expanded from 23.6 +/- 5.96 ml of bone marrow samples. They had normal karyotypes with bi-lineages differentiation potential, and were CD73, CD90, and CD105 positive. Twelve patients underwent cotransplantation with no observable adverse response during and after the infusion of MSCs. Hematopoietic reconstitutions were rapid. Two patients developed grade II-IV acute GVHD, and two extensive chronic GVHD. Four patients suffered from cytomegalovirus infection but were cured eventually. Up to now, seven patients have been followed as long as 29-57 months and five patients died. It is concluded that MSCs can be expanded effectively by culture and it is safe and feasible to cotransplant patients with allogenic culture-expanded MSCs and HSCs.
间充质干细胞(MSCs)可用于支持造血重建,并减轻同种异体造血干细胞(HSCs)移植中的移植物抗宿主病(GVHD)。本研究旨在探讨共输注来自同一人类白细胞抗原(HLA)匹配供者的培养扩增间充质干细胞(MSCs)和 HSCs 在中国血液病患者中的可行性和安全性。从健康供者的骨髓单核细胞进行体外培养和扩增。对共输注来自同一供者的 HSCs 和 MSCs 的患者进行检测,以检测收获的 MSCs 的免疫表型、成脂和成骨分化潜能和核型。观察这些患者共移植后的造血重建、并发症和临床结果。从 23.6 +/- 5.96 ml 的骨髓样本中成功扩增了(1.77 +/- 0.40)x 10(6)/kg(供者体重)的 MSCs。它们具有正常核型和双系分化潜能,CD73、CD90 和 CD105 阳性。12 例患者共输注,在输注 MSCs 期间和之后无观察到不良反应。造血重建迅速。2 例患者发生 II-IV 级急性 GVHD,2 例广泛慢性 GVHD。4 例患者发生巨细胞病毒感染,但最终治愈。迄今为止,7 例患者随访时间长达 29-57 个月,5 例患者死亡。结论是,MSCs 可以通过培养有效扩增,共输注同种异体培养扩增的 MSCs 和 HSCs 是安全可行的。