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人间充质干细胞支持无关供体造血干细胞并抑制T细胞活化。

Human mesenchymal stem cells support unrelated donor hematopoietic stem cells and suppress T-cell activation.

作者信息

Maitra B, Szekely E, Gjini K, Laughlin M J, Dennis J, Haynesworth S E, Koç O N

机构信息

Comprehensive Cancer Center, Case Western Reserve University, University Hospitals of Cleveland, Cleveland, OH 44106, USA.

出版信息

Bone Marrow Transplant. 2004 Mar;33(6):597-604. doi: 10.1038/sj.bmt.1704400.

Abstract

Bone marrow-derived mesenchymal stem cells (MSCs) are known to interact with hematopoietic stem cells (HSCs) and immune cells, and represent potential cellular therapy to enhance allogeneic hematopoietic engraftment and prevent graft-versus-host disease (GVHD). We investigated the role of human MSCs in NOD-SCID mice repopulation by unrelated human hematopoietic cells and studied the immune interactions between human MSCs and unrelated donor blood cells in vitro. When hematopoietic stem cell numbers were limited, human engraftment of NOD-SCID mice was observed only after coinfusion of unrelated human MSCs, but not with coinfusion of mouse mesenchymal cell line. Unrelated human MSCs did not elicit T-cell activation in vitro and suppressed T-cell activation by Tuberculin and unrelated allogeneic lymphocytes in a dose-dependent manner. Cell-free MSC culture supernatant, mouse stromal cells and human dermal fibroblasts did not elicit this effect. These preclinical data suggest that unrelated, human bone marrow-derived, culture-expanded MSCs may improve the outcome of allogeneic transplantation by promoting hematopoietic engraftment and limiting GVHD and their therapeutic potential should be tested in clinic.

摘要

已知骨髓来源的间充质干细胞(MSC)可与造血干细胞(HSC)及免疫细胞相互作用,是增强异基因造血植入及预防移植物抗宿主病(GVHD)的潜在细胞疗法。我们研究了人MSC在非肥胖糖尿病-严重联合免疫缺陷(NOD-SCID)小鼠被无关人造血细胞再植入过程中的作用,并在体外研究了人MSC与无关供体血细胞之间的免疫相互作用。当造血干细胞数量有限时,仅在同时输注无关人MSC后才观察到NOD-SCID小鼠的人源植入,而同时输注小鼠间充质细胞系则未观察到。无关人MSC在体外不会引发T细胞活化,且能以剂量依赖方式抑制结核菌素和无关异基因淋巴细胞引起的T细胞活化。无细胞的MSC培养上清液、小鼠基质细胞和人皮肤成纤维细胞不会产生这种效应。这些临床前数据表明,无关的、人骨髓来源的、经培养扩增的MSC可能通过促进造血植入和限制GVHD来改善异基因移植的结果,其治疗潜力应在临床上进行测试。

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