成人间充质间质细胞与移植物抗宿主病的治疗。

IF 1.7 Q4 CELL BIOLOGY
Stem Cells and Cloning-Advances and Applications Pub Date : 2014-02-28 eCollection Date: 2014-01-01 DOI:10.2147/SCCAA.S37506
Richard P Herrmann, Marian J Sturm
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引用次数: 29

摘要

移植物抗宿主病是造血干细胞移植中一种困难且具有潜在致命性的并发症。它发生于轻微的人白细胞抗原(HLA)错配,通常用皮质类固醇和其他免疫抑制疗法治疗。当类固醇治疗难治性时,死亡率接近80%。间充质间质细胞是在骨髓和其他组织中发现的罕见细胞。它们可以在培养中扩增,具有复杂多样的免疫调节活性。此外,人间充质间质细胞携带低水平的1类HLA抗原,而没有2类HLA抗原,使其具有免疫特权,无需HLA匹配即可使用。2004年首次报道了它们在类固醇难治性移植物抗宿主病中的应用。随后,它们被成功地用于急性和慢性移植物抗宿主病的I期和II期试验。我们讨论了它们的作用方式,结果,它们的产生和潜在的危险,以期将来的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adult human mesenchymal stromal cells and the treatment of graft versus host disease.

Graft versus host disease is a difficult and potentially lethal complication of hematopoietic stem cell transplantation. It occurs with minor human leucocyte antigen (HLA) mismatch and is normally treated with corticosteroid and other immunosuppressive therapy. When it is refractory to steroid therapy, mortality approaches 80%. Mesenchymal stromal cells are rare cells found in bone marrow and other tissues. They can be expanded in culture and possess complex and diverse immunomodulatory activity. Moreover, human mesenchymal stromal cells carry low levels of class 1 and no class 2 HLA antigens, making them immunoprivileged and able to be used without HLA matching. Their use in steroid-refractory graft versus host disease was first described in 2004. Subsequently, they have been used in a number of Phase I and II trials in acute and chronic graft versus host disease trials with success. We discuss their mode of action, the results, their production, and potential dangers with a view to future application.

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来源期刊
CiteScore
6.50
自引率
0.00%
发文量
10
审稿时长
16 weeks
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