首页> 外文期刊>Stem Cells and Development >Infusion of Mesenchymal Stromal Cells can Aid Hematopoietic Recovery Following Allogeneic Hematopoietic Stem Cell Myeloablative Transplant: A Pilot Study
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Infusion of Mesenchymal Stromal Cells can Aid Hematopoietic Recovery Following Allogeneic Hematopoietic Stem Cell Myeloablative Transplant: A Pilot Study

机译:间充质基质细胞的输注可帮助异基因造血干细胞骨髓移植后造血恢复:一项初步研究。

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摘要

Mesenchymal stromal cells (MSCs) are important in the support of hematopoiesis. In this pilot study, we evaluated the safety and efficiency of donor-expanded MSC infusion after allogeneic hematopoietic stem cell transplantation (HSCT) in six patients with poor hematopoietic recovery. MSCs were infused without HSC and without conditioning at a dose of 1 × 106/kg weight. Two patients displayed rapid hematopoietic recovery (days 12 and 21), and four patients showed no response. The two patients who showed hematopoietic recovery were in first complete remission (CR1) compared to the other heavily pretreated patients. There were no toxic side effects linked to MSC infusion. One patient developed cytomegalovirus (CMV) reactivation 12 days following the MSC infusion and died from CMV disease. We found that infusion of MSCs without HSC co-infusion can restore medullary function in some patients with poor hematopoietic recovery. Our data suggest that patients with a less damaged stroma could benefit from this approach.
机译:间充质基质细胞(MSC)在支持造血过程中很重要。在这项前瞻性研究中,我们评估了六名造血恢复较差的异基因造血干细胞移植(HSCT)后供体扩大的MSC输注的安全性和有效性。在无HSC且无条件的情况下以1×10 6 / kg体重的剂量注入MSC。 2名患者表现出快速的造血功能恢复(第12和21天),而4名患者则无反应。与其他经过严格治疗的患者相比,显示出造血功能恢复的两名患者首次完全缓解(CR1)。没有与MSC输注相关的毒性副作用。一名患者在MSC输注后12天出现巨细胞病毒(CMV)活化,并死于CMV疾病。我们发现,在没有造血干细胞共注入的情况下输注MSC可以在造血恢复较差的某些患者中恢复髓质功能。我们的数据表明,基质受损程度较小的患者可以从这种方法中受益。

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  • 来源
    《Stem Cells and Development》 |2009年第9期|1247-1252|共6页
  • 作者单位

    Department of Clinical and Experimental Hematology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.;

    Department of Clinical and Experimental Hematology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.;

    Department of Clinical and Experimental Hematology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.;

    Department of Clinical and Experimental Hematology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.;

    Department of Microbiology and Infectious Diseases, Université Libre de Bruxelles, Brussels, Belgium.;

    Department of Clinical and Experimental Hematology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.;

    Department of Clinical and Experimental Hematology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.;

    Department of Clinical and Experimental Hematology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.;

    Department of Clinical and Experimental Hematology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.;

    Department of Clinical and Experimental Hematology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.;

    Department of Clinical and Experimental Hematology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.;

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