Medical Proteomics Research Center, KRIBB, Daejeon 305-333, Korea.
Exp Mol Med. 2010 Sep 30;42(9):651-61. doi: 10.3858/emm.2010.42.9.065.
Successful hematopoietic stem cell transplantation (HSCT) involves the restoration of hematopoietic function after engraftment, arising from the differentiation and proliferation of hematopoietic stem cells. Several factors could influence the course of allogeneic-HSCT (allo-HSCT). Therefore, knowledge of serum proteome changes during the allo-HSCT period might increase the efficacy of diagnosis and disease prevention efforts. This study conducted proteomic analyses to find proteins that were significantly altered in response to allo-HSCT. Sera from five representative patients who underwent allo-HSCT were analyzed by 2-dimensional gel electrophoresis and liquid chromatography tandem mass spectrometry, and were measured on a weekly basis before and after allo-HSCT in additional 78 patients. Fourteen protein spots showing changes in expression were further examined, and most proteins were identified as acute phase proteins (APPs). Studies of 78 additional patients confirmed that C-reactive protein (CRP) and haptoglobin undergo expression changes during allo-HSCT and thus may have the potential to serve as representative markers of clinical events after allo-HSCT. Maximal CRP level affected the development of major transplant-related complications (MTCs) and other problems such as fever of unknown origin. Particularly, an increase in CRP level 21 days after allo-HSCT was found to be an independent risk factor for MTC. Maximal haptoglobin and haptoglobin level 14 days after allo-HSCT were predictive of relapses in underlying hematologic disease. Our results indicated that CRP and haptoglobin were significantly expressed during allo-HSCT, and suggest that their level can be monitored after allo-HSCT to assess the risks of early transplant-related complications and relapse.
异基因造血干细胞移植(allo-HSCT)的成功涉及到植入后造血功能的恢复,这是由造血干细胞的分化和增殖引起的。有几个因素可能会影响 allo-HSCT 的过程。因此,了解 allo-HSCT 期间血清蛋白质组的变化可能会提高诊断和疾病预防的效果。本研究通过蛋白质组学分析寻找对 allo-HSCT 有明显反应的蛋白质。对 5 名接受 allo-HSCT 的代表性患者的血清进行二维凝胶电泳和液相色谱串联质谱分析,并在另外 78 名患者 allo-HSCT 前后每周进行测量。进一步检查了 14 个表达变化的蛋白质斑点,大多数蛋白质被鉴定为急性相蛋白(APPs)。对 78 名额外患者的研究证实,C 反应蛋白(CRP)和触珠蛋白在 allo-HSCT 期间发生表达变化,因此可能有潜力作为 allo-HSCT 后临床事件的代表性标志物。最大 CRP 水平影响主要移植相关并发症(MTCs)和其他问题的发展,如不明原因发热。特别是,发现 allo-HSCT 后 21 天 CRP 水平的增加是 MTC 的一个独立危险因素。allo-HSCT 后 14 天最大的触珠蛋白和触珠蛋白水平可预测基础血液病的复发。我们的结果表明,CRP 和触珠蛋白在 allo-HSCT 期间明显表达,并表明可以在 allo-HSCT 后监测其水平,以评估早期移植相关并发症和复发的风险。