骨髓纤维化患者用同种异体干细胞移植替代造血系统可诱导骨髓纤维化快速消退。

Fibrogenesis & Tissue Repair Pub Date : 2012-06-06 eCollection Date: 2012-01-01 DOI:10.1186/1755-1536-5-S1-S25
Nicolaus Kröger, Michael Kvasnicka, Jürgen Thiele
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引用次数: 18

摘要

骨髓纤维化是原发性和后ET/PV骨髓纤维化的标志。为了研究同种异体干细胞移植替代骨髓纤维化患者的造血系统对骨髓纤维化的影响,我们研究了来自24名骨髓纤维化患者的骨髓样本在减少剂量后接受相关或非相关供体同种异体干细胞移植前后的骨髓纤维化情况。根据欧洲骨髓纤维化分级共识,在同种异体移植前,所有患者均为晚期纤维化MF-2 (n = 13)或MF-3 (n = 11)。移植后,骨髓纤维化完全(MF-0)或接近完全(MF-1)消退的患者在第100天为59%,第180天为90%,第360天为100%。急性移植物抗宿主病的发生与第180天纤维化消退无相关性。我们得出的结论是,剂量降低后进行同种异体干细胞移植,导致骨髓纤维化的快速消退,这表明骨髓纤维化患者的骨髓纤维化是一个高度动态的过程,而不是静态的过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Replacement of hematopoietic system by allogeneic stem cell transplantation in myelofibrosis patients induces rapid regression of bone marrow fibrosis.

Replacement of hematopoietic system by allogeneic stem cell transplantation in myelofibrosis patients induces rapid regression of bone marrow fibrosis.

Bone marrow fibrosis is a hallmark of primary and post ET/PV myelofibrosis. To investigated the impact of replacement of the hematopoietic system in myelofibrosis patients by allogeneic stem cell transplantation on bone marrow fibrosis, we studied bone marrow fibrosis on bone marrow samples from 24 patients with myelofibrosis before and after dose-reduced conditioning followed by allogeneic stem cell transplantation from related or unrelated donor. Using the European Consensus on Grading Bone Marrow Fibrosis, before allografting all patients had advanced fibrosis MF-2 (n = 13) or MF-3 (n = 11). After transplantation, a complete (MF-0) or nearly complete (MF-1) regression of bone marrow fibrosis was seen in 59 % at day +100, in 90 % at day +180, and in 100 % at day +360. No correlation between occurrence of acute graft-versus-host disease, and fibrosis regression on day +180 was seen. We conclude that dose-reduced conditioning, followed by allogeneic stem cell transplantation, resulted in a rapid resolution of bone-marrow fibrosis suggesting the bone marrow fibrogenesis is a highly dynamic rather than static process in patients with myelofibrosis.

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