严重型再生障碍性贫血患者血清集落刺激活性的研究  被引量:2

Colony stimulating activities of serum from patients with severe aplastic anemia

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作  者:郑以州[1] 储榆林[1] 邵宗鸿[1] 汪永桂[1] 杨萍[1] 田征[1] 汤晓培[1] 张君奎[1] 

机构地区:[1]中国医学科学院中国协和医科大学血液学研究所

出  处:《中华血液学杂志》1997年第4期173-176,共4页Chinese Journal of Hematology

摘  要:目的:探讨严重型再生障碍性贫血(SAA)患者血清集落刺激活性与免疫抑制治疗(IST)疗效的关系。方法:采用造血祖细胞体外培养技术检测SAA患者IST前后和健康献血员血清体外红系爆式集落刺激活性(BPA)及粒-巨噬细胞系集落刺激活性(GM-CSA),并用酶联免疫法(ELISA)检测了本组患者IST前后和正常对照组血清红细胞生成素(Epo)水平。结果:初诊SAA患者血清BPA较正常对照显著增强(P<0.001);22例SAA患者中13例(59.0%)血清GM-CSA正常,9例(41.0%)较正常明显降低;IST后SAA患者血清BPA及GM-CSA均无明显变化;初诊时SAA患者血清GM-CSA水平高低与IST疗效密切相关,血清GM-CSA水平正常者IST疗效显著优于明显降低者(P<0.01);SAA患者IST前血清Epo水平显著高于正常对照(P<0.001),IST后有效者血清Epo水平明显下降,但仍显著高于正常对照者(P<0.001),而无效者血清Epo水平有进一步增高趋势。结论:初诊时SAA患者血清GM-CSA个体间差异较大,其血清GM-CSA高低与IST疗效密切相关;初诊SAA患者血清BPA及Epo水平较正?Objective:To investigate the correlation between colony stimulating activities of serum from patients with severe aplastic anemia (SAA) and their responses to immunosuppressive therapy (IST). Methods: In vitro effects of sera from SAA patients before and after IST and from normal subjects on human marrow colony growth were examined in a semisolid methylcellulose culture system for burst promoting activity (BPA) and granulocyte/macrophage colony stimulating activity (GM CSA).Serum erythropoietin (Epo) level was also measured by ELISA method before and after IST in SAA patients. Results: Serum BPAs in SAA patients at diagnosis were significantly higher than that in normal controls (P<0.001),but serum GM CSAs in 13 of 22 SAA patients were normal,and in 9 of 22 extremely low as compared with normal values.After IST, serum BPA and GM CSA in SAA patients had no changes. Serum Epo levels in SAA patients at diagnosis were significantly higher than that in normal controls (P<0.001).After IST,serum Epo levels declined in responded patients, while further increased in nonresponded . Conclusion: Serum GM CSA of SAA patients was a predictive factor for responsiveness to IST, and a normal value was associated with a good response.

关 键 词:再生障碍性贫血 集落刺激活性 

分 类 号:R556.502[医药卫生—血液循环系统疾病]

 

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