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5q缺失的骨髓增生异常综合征中造血祖细胞/干细胞的分离与鉴定:造血干细胞水平受累的证据

Isolation and characterization of hematopoietic progenitor/stem cells in 5q-deleted myelodysplastic syndromes: evidence for involvement at the hematopoietic stem cell level.

作者信息

Nilsson L, Astrand-Grundström I, Arvidsson I, Jacobsson B, Hellström-Lindberg E, Hast R, Jacobsen S E

机构信息

Stem Cell Laboratory, Institute of Laboratory Medicine, and the Department of Hematology, Lund University Hospital, Lund, Sweden.

出版信息

Blood. 2000 Sep 15;96(6):2012-21.

PMID:10979941
Abstract

Myelodysplastic syndromes (MDS) are a heterogeneous group of clonal disorders characterized by ineffective hematopoiesis and frequent progression to acute myeloid leukemia. Within MDS, 5q- syndrome constitutes a distinct clinical entity characterized by an isolated deletion of the long arm of chromosome 5 (5q-), a relatively good prognosis, and infrequent transformation to acute leukemia. The cell of origin in 5q- syndrome as well as in other 5q-deleted MDS patients has not been established, but evidence for involvement of multiple myeloid (but not lymphoid) lineages has suggested that a myeloid-restricted progenitor rather than a pluripotent (lympho-myeloid) stem cell might be the primary target in most patients. Although in 9 patients no evidence of peripheral blood T-cell and only 1 case of B-cell involvement was found, the data herein support that 5q deletions occur in hematopoietic stem cells (HSCs) with a combined lympho-myeloid potential. First, in all investigated patients a minimum of 94% of cells in the minor CD34(+)CD38(-) HSC compartment were 5q deleted as determined by fluorescence in situ hybridization. Second, in 3 of 5 patients 5q aberrations were detected in a large fraction (25% to 90%) of purified CD34(+)CD19(+) pro-B cells. Furthermore, extensive functional characterization with regard to responsiveness to early-acting cytokines, long-term culture-initiating cells, and nonobese diabetic/severe combined immunodeficiency repopulating cells supported that MDS HSCs in 5q-deleted patients are CD34(+)CD38(-), but inefficient at reconstituting hematopoiesis.

摘要

骨髓增生异常综合征(MDS)是一组异质性克隆性疾病,其特征为造血无效以及频繁进展为急性髓系白血病。在MDS中,5q-综合征构成一种独特的临床实体,其特征为染色体5长臂(5q-)的孤立性缺失、相对较好的预后以及很少转化为急性白血病。5q-综合征以及其他5q缺失的MDS患者的起源细胞尚未明确,但多系髓系(而非淋巴系)受累的证据提示,在大多数患者中,髓系限制性祖细胞而非多能(淋巴-髓系)干细胞可能是主要靶点。尽管在9例患者中未发现外周血T细胞受累的证据,仅1例发现B细胞受累,但本文数据支持5q缺失发生在具有淋巴-髓系联合潜能的造血干细胞(HSC)中。首先,通过荧光原位杂交测定,在所有研究患者中,至少94%的小部分CD34(+)CD38(-) HSC区室细胞存在5q缺失。其次,在5例患者中的3例中,在大部分(25%至90%)纯化的CD34(+)CD19(+)前B细胞中检测到5q畸变。此外,关于对早期作用细胞因子的反应性、长期培养起始细胞和非肥胖糖尿病/严重联合免疫缺陷再植细胞的广泛功能特征支持,5q缺失患者的MDS HSC是CD34(+)CD38(-),但在重建造血方面效率低下。

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