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再生障碍性贫血患者的血小板生成素血清水平:与血小板计数的相关性及缓解期的持续升高

Thrombopoietin serum levels in patients with aplastic anaemia: correlation with platelet count and persistent elevation in remission.

作者信息

Schrezenmeier H, Griesshammer M, Hornkohl A, Nichol J L, Hecht T, Heimpel H, Kubanek B, Raghavachar A

机构信息

Department of Internal Medicine III, University of Ulm, Germany.

出版信息

Br J Haematol. 1998 Mar;100(3):571-6. doi: 10.1046/j.1365-2141.1998.00590.x.

Abstract

In an attempt to evaluate the role of thrombopoietin (TPO) in the pathobiology of aplastic anaemia (AA), we have examined TPO levels in sera from 54 AA patients and 119 healthy controls. A total of 92 samples were collected from AA patients: 43 samples were harvested at diagnosis, 23 samples in the cytopenic period after treatment, and 26 samples when patients were in partial (n=10) or complete remission (n=16) following immunosuppressive treatment. TPO serum levels were assessed by a sandwich-antibody ELISA that utilized a polyclonal rabbit antiserum for both capture and signal. Serum samples from normal donors revealed a mean TPO level of 95.3 +/- 54.0 pg/ml (standard deviation). Mean TPO levels in AA sera collected at diagnosis and before onset of treatment were 2728 +/- 1074 pg/ml (P<0.001 compared to normal controls: mean platelet count at that time: 27x10(9)/l). TPO serum levels of AA patients in partial or complete remission after immunosuppressive treatment were significantly lower than TPO levels at diagnosis (P<0.001). However, despite normal platelet counts (mean 167x10(9)/l), TPO levels remained significantly elevated in complete remission (mean TPO 1009 +/- 590 pg/ml, P<0.001 compared to normal controls). There was a significant inverse correlation between serum TPO levels and platelet counts in AA patients who were not transfused for at least 2 weeks prior to sample collection (coefficient of correlation (r) = -0.70, P<0.0001). In summary, TPO levels were highly elevated in sera of patients with AA. Thus there is no evidence to suggest an impaired TPO response contributing to thrombocytopenia in AA. Thrombopoietin did not return to normal levels in remission, indicating a persisting haemopoietic defect in remission of AA. We hypothesize that elevated levels of TPO may be required to maintain normal or near normal platelet counts in remission of AA.

摘要

为了评估血小板生成素(TPO)在再生障碍性贫血(AA)病理生物学中的作用,我们检测了54例AA患者和119例健康对照者血清中的TPO水平。共从AA患者中采集了92份样本:43份样本在诊断时采集,23份样本在治疗后的血细胞减少期采集,26份样本在患者接受免疫抑制治疗后处于部分缓解(n = 10)或完全缓解(n = 16)时采集。采用双抗体夹心ELISA法评估TPO血清水平,该方法使用多克隆兔抗血清进行捕获和信号检测。正常供者的血清样本显示TPO平均水平为95.3±54.0 pg/ml(标准差)。诊断时及治疗开始前采集的AA血清中TPO平均水平为2728±1074 pg/ml(与正常对照相比,P<0.001;当时的平均血小板计数为27×10⁹/L)。免疫抑制治疗后处于部分或完全缓解的AA患者的TPO血清水平显著低于诊断时的水平(P<0.001)。然而,尽管血小板计数正常(平均167×10⁹/L),完全缓解时TPO水平仍显著升高(平均TPO为1009±590 pg/ml,与正常对照相比,P<0.001)。在样本采集前至少2周未输血的AA患者中,血清TPO水平与血小板计数之间存在显著的负相关(相关系数(r)=-0.70,P<0.0001)。总之,AA患者血清中TPO水平显著升高。因此,没有证据表明TPO反应受损导致AA患者血小板减少。血小板生成素在缓解期未恢复到正常水平,表明AA缓解期存在持续的造血缺陷。我们推测,AA缓解期可能需要升高的TPO水平来维持正常或接近正常的血小板计数。

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