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用于实体器官与骨髓联合移植的椎体骨髓中的造血祖细胞含量

Hematopoietic progenitor cell content of vertebral body marrow used for combined solid organ and bone marrow transplantation.

作者信息

Rybka W B, Fontes P A, Rao A S, Winkelstein A, Ricordi C, Ball E D, Starzl T E

机构信息

Bone Marrow Transplant Program, Pittsburgh Cancer Institute, USA.

出版信息

Transplantation. 1995 Mar 27;59(6):871-4. doi: 10.1097/00007890-199503270-00012.

Abstract

While cadaveric vertebral bodies (VB) have long been proposed as a suitable source of bone marrow (BM) for transplantation (BMT), they have rarely been used for this purpose. We have infused VB BM immediately following whole organ (WO) transplantation to augment donor cell chimerism. We quantified the hematopoietic progenitor cell (HPC) content of VB BM as well as BM obtained from the iliac crests (IC) of normal allogenic donors (ALLO) and from patients with malignancy undergoing autologous marrow harvest (AUTO). Patients undergoing WO/BM transplantation also had AUTO BM harvested in the event that subsequent lymphohematopoietic reconstitution was required. Twenty-four VB BM, 24 IC BM-ALLO, 31 IC AUTO, and 24 IC WO-AUTO were harvested. VB BM was tested 12 to 72 hr after procurement and infused after completion of WO grafting. IC BM was tested and then used or cryopreserved immediately. HPC were quantified by clonal assay measuring CFU-GM, BFU-E, and CFU-GEMM, and by flow cytometry for CD34+ progenitor cells. On an average, 9 VB were processed during each harvest, and despite an extended processing time the number of viable nucleated cells obtained was significantly higher than that from IC. Furthermore, by HPC content, VB BM was equivalent to IC BM, which is routinely used for BMT. We conclude that VB BM is a clinically valuable source of BM for allogeneic transplantation.

摘要

虽然长期以来一直有人提出将尸体椎体(VB)作为适合用于移植(BMT)的骨髓(BM)来源,但它们很少被用于此目的。我们在全器官(WO)移植后立即输注VB骨髓,以增强供体细胞嵌合。我们对VB骨髓以及从正常同种异体供体(ALLO)的髂嵴(IC)和接受自体骨髓采集(AUTO)的恶性肿瘤患者获得的骨髓中的造血祖细胞(HPC)含量进行了量化。接受WO/BM移植的患者也采集了AUTO骨髓,以备后续需要淋巴细胞造血重建时使用。共采集了24份VB骨髓、24份IC骨髓-ALLO、31份IC AUTO和24份IC WO-AUTO。VB骨髓在采集后12至72小时进行检测,并在WO移植完成后输注。IC骨髓进行检测后立即使用或冷冻保存。通过测量CFU-GM、BFU-E和CFU-GEMM的克隆分析以及对CD34+祖细胞进行流式细胞术来量化HPC。每次采集平均处理9个VB,尽管处理时间延长,但获得的活有核细胞数量显著高于IC骨髓。此外,就HPC含量而言,VB骨髓与常规用于BMT的IC骨髓相当。我们得出结论,VB骨髓是同种异体移植中具有临床价值的骨髓来源。

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