Angiogenic Factors Are Associated with Development of Acute Graft-Versus-Host Disease after Allogeneic Hematopoietic Stem Cell Transplantation

被引:0
|
作者
聂第敏 [1 ]
吴秋玲 [1 ]
朱夏夏 [1 ]
张然 [1 ]
郑鹏 [1 ]
方俊 [1 ]
游泳 [1 ]
仲照东 [1 ]
夏凌辉 [1 ]
洪梅 [1 ]
机构
[1] Institute of Hematology,Union Hospital,Tongji Medical College,Huazhong University of Science and Technology
基金
中国国家自然科学基金;
关键词
allogeneic hematopoietic stem cell transplantation; acute graft-versus-host disease; angiogenic factors; endothelial damage;
D O I
暂无
中图分类号
R457.7 [骨髓移植];
学科分类号
100215 ;
摘要
Acute graft-versus-host disease(a GVHD) is a serious complication after allogeneic hematopoietic stem cell transplantation(allo-HSCT). However,the mechanisms of a GVHD are not well understood. We aim to investigate the roles of the three angiogenic factors: angiopoietin-1(Ang-1),Ang-2 and vascular endothelial growth factor(VEGF) in the development of a GVHD. Twenty-one patients who underwent allo-HSCT were included in our study. The dynamic changes of Ang-1,Ang-2 and VEGF were monitored in patients before and after allo-HSCT. In vitro,endothelial cells(ECs) were treated with TNF-α in the presence or absence of Ang-1,and then the Ang-2 level in the cell culture medium and the tubule formation by ECs were evaluated. After allo-HSCT,Ang-1,Ang-2 and VEGF all exhibited significant variation,suggesting these factors might be involved in the endothelial damage in transplantation. Patients with a GVHD had lower Ang-1 level at day 7 but higher Ang-2 level at day 21 than those without a GVHD,implying that Ang-1 may play a protective role in early phase yet Ang-2 is a promotion factor to a GVHD. In vitro,TNF-α promoted the release of Ang-2 by ECs and impaired tubule formation of ECs,which were both weakened by Ang-1,suggesting that Ang-1 may play a protective role in a GVHD by influencing the secretion of Ang-2,consistent with our in vivo tests. It is concluded that monitoring changes of these factors following allo-HSCT might help to identify patients at a high risk for a GVHD.
引用
收藏
页码:694 / 699
页数:6
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