期刊文献+

再生障碍性贫血患者骨髓祖细胞培养的临床意义 被引量:1

Clinical significance and culture of hematopoietic progenitor cells in aplastic anemia
下载PDF
导出
摘要 目的探讨再生障碍性贫血(AA)患者红细胞集落生成单位(CFU-E)、爆式红细胞集落生成单位(BFU-E)、粒细胞-单核细胞集落生成单位(CFU-GM)及巨核细胞集落生成单位(CFU-Meg)骨髓祖细胞培养情况。方法抽取39例AA患者骨髓分别作四类祖细胞培养,在7d、14d测定其集落数,与同期住院非血液病患者比较。结果39例再障患者四类集落数均值与对照组比较,差异有统计学意义(P<0.01或P<0.001)。集落数随着病情加重而逐步下降。治愈及进步者四类集落数接近对照组水平,治疗无效及进展者与治疗前比较差异无统计学意义。结论部分AA患者存在四类祖细胞培养集落数的降低,基本与患者的病情严重程度呈正比。动态监测AA患者骨髓四类祖细胞集落数的变化对辅助诊断、观察疗效及预后判断均有指导意义。 Objective To study hematopoietie progenitor cells(HPC) proliferation through detection of blast-forming-unit of erythyroeyte (BFU-E), colony forming-unit of erythroeyte ( CFU-E ), colony-forming-unit of granuloeyte-monoeyte ( CFU-GM ) and colony-forming-unit of megakayocyte(CFU-Meg) by HPC culture of bone marrow(BM) from aplastie anemia(AA). Methods Detecting BFU:E,CFU-E, CFU-GM and CFU-Meg at 7 d, 14 d after cellular culture from 39 eases with AA. Results The mean values of four different colonies in 39 patients were significandy lower than those of the control. The mean decrease of these colonies was positively correlated with the severity of the types of diseases.Conclusion A portion of eases with AA have lower quantities of BFU-E, CFU-E, CFU-GM and CFU-Meg, and the quantitative decrease in these color hies is positively correlated with severity of the disease. Testing the changes of BFU-E,CFU-E,CFU-GM and CFU-Meg by HPC culture has significance to the diagnosis, effect observeing and prognosis judging.
作者 李虎生
出处 《内科》 2008年第4期504-506,共3页 Internal Medicine
关键词 再生障碍性贫血 骨髓祖细胞 治疗 Aplastie anemia Hematopoietie progenitor cells Treatment
  • 相关文献

参考文献5

二级参考文献54

  • 1何广胜,邵宗鸿,和虹,刘鸿,付蓉,白洁,施均,曹燕然,涂梅峰,孙娟,贾海荣.重型再生障碍性贫血患者骨髓Ⅰ型树突细胞亚群的变化[J].中华血液学杂志,2004,25(11):649-652. 被引量:10
  • 2郑以州,邵宗鸿,储榆林.再生障碍性贫血造血干/祖细胞缺陷研究进展[J].中华血液学杂志,1996,17(4):219-222. 被引量:5
  • 3第四届全国再生障碍性贫血学术会议.再生障碍性贫血诊断标准[J].中华血液学杂志,1987,(8).
  • 4Kagan WA, Ascensao JL, Fialk MA, et al. Studies on the pathogenesis of aplastic anemia [J]. The American Journal of Medicine, 1979, 66(3): 444-449.
  • 5Rizzo S, Scopes J, Elebute MA, et al. Stem cell defect in aplastic anemia: reduced long term culture-initiating cells (LTC-IC) in CD34+ cells isolated from aplastic anemia patient bone marrow [J]. Hematol J, 2002, 3(5): 230-236.
  • 6Karakantza M, Cavenagh JD, Gordon-Smith EC, et al. Adhesion molecule expression on CD34+ progenitor cells from normal and aplastic anaemia bone marrow [J].Br J Haematol,1995,91(4): 800-803.
  • 7Novitzky N, Jacobs P. Immunosuppressive therapy in bone marrow aplasia: the stroma functions normally to support hematopoiesis [J]. Exp Hematol,1995, 23(14): 1472-1477.
  • 8Manz CY, Missen C, Wodnar-Filipowicz A. Deficiency of CD34+ c-kit+ and CD34+ 38- gematopoietic precursors in aplastic anemia after immunosuppressive treatment [J]. Am J Hematol,1996, 52(4): 264-274.
  • 9Goldenberg NA,Graham DK,Liang X,et al.Successful treatment of severe aplastic anemia in children using standardized immunosuppressive therapy with antithymocyte globulin and cyclosporine A.Pediatr Blood Cancer,2004,43:718-722.
  • 10Zeng W,Maciejewski JP,Chen G,et al.Limited heterogeneity of T cell receptor BV usage in aplastic anemia.J Clin Invest,2001,108:765 -773.

共引文献106

同被引文献12

引证文献1

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部