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评价 ALL 患者骨髓移植前后循环中 CXCL1(Gro-α)、CXCL10(IP-10)和 CXCL12(SDF-1)的浓度。

Evaluation of circulating concentrations of CXCL1 (Gro-α), CXCL10 (IP-10) and CXCL12 (SDF-1) in ALL patients prior and post bone marrow transplantation.

机构信息

Department of Hematology-Oncology and BMT, Kerman University of Medical Sciences, Kerman, Iran.

出版信息

Pathol Res Pract. 2012 Oct 15;208(10):615-9. doi: 10.1016/j.prp.2012.06.009. Epub 2012 Sep 10.

Abstract

The immune system plays an important role in the development of leukemia. CXC chemokines, as the molecular members of this system, are involved in the immune responses. Therefore, this study was designed to examine and compare the levels of CXCL1 (Gro-α), CXCL10 (IP-10) and CXCL12 (SDF-1) in ALL patients prior to and post bone marrow transplantation (BMT). In this experimental study, samples were obtained from ALL patients and controls, and subjected to ELISA for detection of chemokines. Demographic data were also collected by a questionnaire. Data were analyzed using SPSS software. Our results showed that the serum levels of CXCL1 (Gro-α), CXCL10 (IP-10) and CXCL12 (SDF-1) were significantly increased in ALL patients compared to the controls. We also showed that the CXCL10 (IP-10) level was increased after BMT in ALL patients, while CXCL1 (Gro-α) and CXCL12 (SDF-1) were inversely decreased. Our results allow for the conclusion that CXCL1 (Gro-α), CXCL10 (IP-10) and CXCL12 (SDF-1) are important for the pathogenesis of ALL. Notably, these chemokines might be used as pivotal biological markers in the diagnosis of leukemia. Recombinant CXCL1 (Gro-α), CXCL10 (IP-10) and CXCL12 (SDF-1) may be applied as a therapeutic approach in the treatment of leukemia patients.

摘要

免疫系统在白血病的发展中起着重要作用。CXC 趋化因子作为该系统的分子成员,参与免疫反应。因此,本研究旨在检查和比较 ALL 患者骨髓移植(BMT)前后 CXCL1(Gro-α)、CXCL10(IP-10)和 CXCL12(SDF-1)的水平。在这项实验研究中,从 ALL 患者和对照组中采集样本,并通过 ELISA 检测趋化因子。还通过问卷收集人口统计学数据。使用 SPSS 软件分析数据。我们的结果表明,与对照组相比,ALL 患者血清中 CXCL1(Gro-α)、CXCL10(IP-10)和 CXCL12(SDF-1)的水平显著升高。我们还表明,ALL 患者 BMT 后 CXCL10(IP-10)水平升高,而 CXCL1(Gro-α)和 CXCL12(SDF-1)水平则相反下降。我们的结果表明,CXCL1(Gro-α)、CXCL10(IP-10)和 CXCL12(SDF-1)对 ALL 的发病机制很重要。值得注意的是,这些趋化因子可能被用作白血病诊断的关键生物学标志物。重组 CXCL1(Gro-α)、CXCL10(IP-10)和 CXCL12(SDF-1)可作为治疗白血病患者的一种治疗方法。

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