O'Flaherty E, Sparrow R, Szer J
Clinical Haematology and Bone Marrow Transplantation, Alfred Hospital, Prahran, Victoria, Australia.
Bone Marrow Transplant. 1995 Feb;15(2):207-12.
A two-stage long-term bone marrow culture (LTBMC) has been used to assess haemopoietic supporting ability from patients following allogeneic bone marrow transplantation (BMT). Irradiated confluent LTBMCs derived from recipients following BMT were recharged with flow cytometry sorted CD34+/CD38- cells from normal BM donors. The output of granulocyte/macrophage colony-forming cells (GM-CFC) in the non-adherent fraction of the cultures was monitored weekly until output ceased. Patient stromal cell function was determined by comparing the percentage of the total cumulative GM-CFC output to the output from normal control stroma. Neutrophil recovery was rapid and complete early in the post-transplant period. However, in contrast, GM-CFC recovery was significantly reduced in all patients up to 5 years after BMT. In 58% of patients studied following BMT the BM stroma is considerably compromised in its ability to support early uncommitted haemopoietic cells contained within the CD34+/CD38- cell fraction of normal BM. Bone marrow stroma from BMT recipients exhibited severe deficits in their abilities to support primitive haemopoietic cells and in some patients this effect lasted for several years. While the growth of stroma from patients following BMT was severely delayed and often incomplete, characterisation of cells types using APAAP techniques did not show significant differences in proportion when compared with normal cultures.(ABSTRACT TRUNCATED AT 250 WORDS)
两阶段长期骨髓培养(LTBMC)已被用于评估异基因骨髓移植(BMT)后患者的造血支持能力。对BMT后受者来源的经辐照的汇合LTBMC,用来自正常骨髓供体的经流式细胞术分选的CD34+/CD38-细胞进行再填充。每周监测培养物非贴壁部分中粒细胞/巨噬细胞集落形成细胞(GM-CFC)的产出,直至产出停止。通过比较总累积GM-CFC产出的百分比与正常对照基质的产出,来确定患者基质细胞功能。移植后早期中性粒细胞恢复迅速且完全。然而,相比之下,BMT后长达5年的所有患者中GM-CFC恢复均显著降低。在BMT后接受研究的患者中,58%的患者骨髓基质支持正常骨髓CD34+/CD38-细胞部分中早期未定向造血细胞的能力受到相当大的损害。BMT受者的骨髓基质在支持原始造血细胞方面表现出严重缺陷,在一些患者中这种影响持续数年。虽然BMT后患者的基质生长严重延迟且往往不完全,但与正常培养物相比,使用碱性磷酸酶抗碱性磷酸酶(APAAP)技术对细胞类型进行表征时,比例上未显示出显著差异。(摘要截短于250字)