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Use of mesenchymal cells to modulate immune suppression and immune reconstruction in a patient with aplastic anemia complicated by invasive sino-orbital aspergillosis.应用间充质细胞调节再生障碍性贫血合并侵袭性鼻窦眶部曲霉菌病患者的免疫抑制和免疫重建。
Turk J Haematol. 2014 Jun;31(2):181-3. doi: 10.4274/tjh.2013.0041. Epub 2014 Jun 10.
2
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Bone marrow mesenchymal stem cells from patients with aplastic anemia maintain functional and immune properties and do not contribute to the pathogenesis of the disease.再生障碍性贫血患者的骨髓间充质干细胞保持功能和免疫特性,且不参与该疾病的发病机制。
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Blood. 2006 Sep 15;108(6):2114-20. doi: 10.1182/blood-2005-11-011650. Epub 2006 May 11.
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[Clinical application of mesenchymal stem cells for hematological diseases].间充质干细胞在血液系统疾病中的临床应用
Rinsho Ketsueki. 2018;59(10):2362-2372. doi: 10.11406/rinketsu.59.2362.
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Cotransplantation of bone marrow-derived mesenchymal stem cells in haploidentical hematopoietic stem cell transplantation in patients with severe aplastic anemia: an interim summary for a multicenter phase II trial results.骨髓间充质干细胞共移植用于重型再生障碍性贫血患者单倍体相合造血干细胞移植:一项多中心II期试验结果的中期总结
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Related HLA-mismatched/haploidentical hematopoietic stem cell transplantation without in vitro T-cell depletion: observations of a single Chinese center.无关供者HLA错配/单倍型相合非体外去除T细胞的造血干细胞移植:单中心中国经验
Clin Transpl. 2011:237-45.
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Hematopoietic stem cell transplantation with umbilical cord multipotent stromal cell infusion for the treatment of aplastic anemia--a single-center experience.脐带间充质干细胞输注联合造血干细胞移植治疗再生障碍性贫血的单中心经验。
Cytotherapy. 2013 Sep;15(9):1118-25. doi: 10.1016/j.jcyt.2013.04.007. Epub 2013 Jun 25.

引用本文的文献

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[Graft failure in allogeneic hematopoietic stem cell trans-plantation].[异基因造血干细胞移植中的移植物失败]
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2018 Dec 25;47(6):651-658. doi: 10.3785/j.issn.1008-9292.2018.12.14.
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Hematopoietic Stem Cell Transplantation in Adult Sickle Cell Disease: Problems and Solutions.成人镰状细胞病的造血干细胞移植:问题与解决方案
Turk J Haematol. 2015 Sep;32(3):195-205. doi: 10.4274/tjh.2014.0311.

本文引用的文献

1
Allogeneic stem cell transplant in a patient with aplastic anemia with bacteremia and candidemia.一名再生障碍性贫血合并菌血症和念珠菌血症患者的异基因干细胞移植。
Turk J Haematol. 2008 Dec 5;25(4):209-10.
2
Role of mesenchymal stem cells in immunological rejection of organ transplantation.间充质干细胞在器官移植免疫排斥中的作用。
Stem Cell Rev Rep. 2009 Dec;5(4):402-9. doi: 10.1007/s12015-009-9076-y. Epub 2009 Jun 19.
3
Infusion of mesenchymal stromal cells can aid hematopoietic recovery following allogeneic hematopoietic stem cell myeloablative transplant: a pilot study.间充质基质细胞输注可促进异基因造血干细胞清髓性移植后的造血恢复:一项初步研究。
Stem Cells Dev. 2009 Nov;18(9):1247-52. doi: 10.1089/scd.2009.0029.
4
Risk factors for invasive aspergillosis and related mortality in recipients of allogeneic SCT from alternative donors: an analysis of 306 patients.来自替代供体的异基因造血干细胞移植受者侵袭性曲霉病及相关死亡率的危险因素:306例患者分析
Bone Marrow Transplant. 2009 Sep;44(6):361-70. doi: 10.1038/bmt.2009.39. Epub 2009 Mar 23.
5
Mesenchymal stem cells for treatment of steroid-resistant, severe, acute graft-versus-host disease: a phase II study.间充质干细胞治疗类固醇难治性重度急性移植物抗宿主病:一项II期研究。
Lancet. 2008 May 10;371(9624):1579-86. doi: 10.1016/S0140-6736(08)60690-X.
6
Cotransplantation of ex vivo expanded mesenchymal stem cells accelerates lymphocyte recovery and may reduce the risk of graft failure in haploidentical hematopoietic stem-cell transplantation.体外扩增的间充质干细胞共移植可加速淋巴细胞恢复,并可能降低单倍体造血干细胞移植中移植物失败的风险。
Blood. 2007 Oct 1;110(7):2764-7. doi: 10.1182/blood-2007-04-087056. Epub 2007 Jul 16.
7
Transplantation of mesenchymal stem cells to enhance engraftment of hematopoietic stem cells.间充质干细胞移植以增强造血干细胞的植入。
Leukemia. 2007 Aug;21(8):1733-8. doi: 10.1038/sj.leu.2404777. Epub 2007 May 31.
8
Mesenchymal stem cells for treatment of therapy-resistant graft-versus-host disease.间充质干细胞用于治疗难治性移植物抗宿主病
Transplantation. 2006 May 27;81(10):1390-7. doi: 10.1097/01.tp.0000214462.63943.14.
9
The role of mesenchymal stem cells in haemopoiesis.间充质干细胞在造血过程中的作用。
Blood Rev. 2006 May;20(3):161-71. doi: 10.1016/j.blre.2005.11.002. Epub 2005 Dec 20.
10
Treatment of severe acute graft-versus-host disease with third party haploidentical mesenchymal stem cells.用第三方单倍体相合间充质干细胞治疗严重急性移植物抗宿主病
Lancet. 2004 May 1;363(9419):1439-41. doi: 10.1016/S0140-6736(04)16104-7.

应用间充质细胞调节再生障碍性贫血合并侵袭性鼻窦眶部曲霉菌病患者的免疫抑制和免疫重建。

Use of mesenchymal cells to modulate immune suppression and immune reconstruction in a patient with aplastic anemia complicated by invasive sino-orbital aspergillosis.

机构信息

Başkent University Adana Adult Bone Marrow Transplantation and Stem Cell Therapy Center, Department of Hematology, Adana, Turkey.

Başkent University Adana Adult Bone Marrow Transplantation and Stem Cell Therapy Center, Department of Hematology, Adana, Turkey ; Başkent University Adana Adult Bone Marrow Transplantation and Stem Cell Therapy Center, Department of Physiology, Ankara, Turkey.

出版信息

Turk J Haematol. 2014 Jun;31(2):181-3. doi: 10.4274/tjh.2013.0041. Epub 2014 Jun 10.

DOI:10.4274/tjh.2013.0041
PMID:25035677
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4102047/
Abstract

Cultured human bone marrow mesenchymal cells (MSCs) have immunomodulatory and tissue regenerative properties. This report summarizes the result of post-transplant treatment with MSCs of a 26-year-old patient with aplastic anemia complicated by invasive sino-orbital aspergillosis. The patient was treated with MSCs to benefit from the dual effects of MSCs in immune reconstitution: suppression against alloreactive T cells and facilitation of the re-engraftment process. The patient did not develop acute or chronic graft-versus-host disease. The aspergillus infection healed completely. The engraftment failure was also ended without any complications. During his last visit in his fourth year after transplantation, the patient was in hematological remission. Human bone marrow-derived MSCs seem to have an important role in preventing or overcoming immunological complications in patients who undergo stem cell transplantation.

摘要

培养的人骨髓间充质细胞(MSCs)具有免疫调节和组织再生特性。本报告总结了一名 26 岁再生障碍性贫血合并侵袭性鼻窦眼眶曲霉病患者接受 MSC 移植后治疗的结果。该患者接受 MSC 治疗,以受益于 MSC 在免疫重建中的双重作用:抑制同种反应性 T 细胞和促进再植入过程。患者未发生急性或慢性移植物抗宿主病。曲霉感染完全愈合。植入失败也没有任何并发症而结束。在移植后第四年的最后一次就诊时,患者处于血液学缓解状态。人骨髓来源的 MSC 似乎在预防或克服干细胞移植患者的免疫并发症方面具有重要作用。