期刊文献+

自体外周血干细胞移植对乙肝相关终末期肝病患者免疫功能的调节作用 被引量:6

Immunoregulation of autologous peripheral blood stem cell transplantation in patients with hepatitis B-related end-stage liver disease
下载PDF
导出
摘要 目的探讨自体外周血干细胞移植对乙型肝炎病毒(HBV)相关终末期肝病患者外周血中T淋巴细胞亚群和细胞因子的免疫调节作用。方法采用流式细胞术检测患者外周血中Th1、Th2、调节性T细胞(Treg)的百分比,ELISA检测血浆IFN-γ、IL-6、IL-10水平。结果自体外周血干细胞移植能明显改善HBV相关终末期肝病患者肝功能,同时上调患者外周血中Th2、Treg的百分比,下调血浆IL-6和IL-10水平(P<0.05),而对Th1细胞及其细胞因子IFN-γ影响无统计学意义。结论自体外周血干细胞移植可能是通过调节机体免疫微环境,抑制肝脏炎症反应,从而改善HBV相关终末期肝病患者肝功能。 Objective To investigate the immunoregulatory effect of autologous peripheral blood stem cells (PBSCs) transplantation on T lymphocytes and cytokines in patients with HBV-related end-stage liver disease. Methods Row cytometry was used to measure the percentages of ThI, Th2 and regulatory T cells (Treg) in peripheral blood. Enzyme-linked immunosor- bent assay (ELISA) was performed to analyze the levels of serum IFN-γ, IL-6 and IL-10. Results Patients with HBV-related end-stage liver disease displayed significantly improved liver function after PBSCs transplantation. Statistically, after PBSCs transplantation, the percentages of Th2 and Treg in peripheral blood markedly increased, but serum IL-6 and IL-10 declined significantly. No significant differences were observed in the changes of Th1 and its cytokine, IFN-γ after transplantation. ConclusionAutologous PBSCs transplantation can depress inflammation in liver by regulating immune microenvironment, which at least in part delineates the mechanism of stem cells-mediated therapeutic benefit on end-stage liver disease.
出处 《细胞与分子免疫学杂志》 CAS CSCD 北大核心 2013年第4期407-410,共4页 Chinese Journal of Cellular and Molecular Immunology
基金 国家高技术研究发展计划(863)资助(2011AA020111)
关键词 HBV 终末期肝病 外周血干细胞 T淋巴细胞 细胞因子 HBV end-stage liver disease peripheral blood stem cells T lymphocyte cytokine
  • 相关文献

参考文献13

  • 1Liu J, Fan D. Hepatitis B in China [ J]. Lancet, 2007, 369 (9573) : 1582 - 1583.
  • 2Han Y, Yan L, Han G, et al. Controlled trials in hepatitis B virus- related deeompensate liver cirrhosis: peripheral blood monoeytetransplant versus granulocyte-colony-stimulating factor mobilization therapy[J]. Cytotherapy, 2008, 10(4): 390-396.
  • 3Pal M, Spalding D, Xi F, et al. Antologous bone marww stem cells in the treatment of chronic liver disease [ J/OA ]. Int J Hepatol, 2012, 2012: 307165.
  • 4Hao L, Sun H, Wang J, et al. Mesenchymal stromal cells for cell therapy: besides supporting hematopoiesis [ J ]. Int J Hematol, 2012, 95(1) : 34 -46.
  • 5Gala S, Smedile A, Omede P, et al. Feasibility and safety of G- CSF administration to induce bone marrow-derived cells mobiliza- tion in patients with end stage liver disease[J]. J Hepatol, 2006, 45(1) : 13 -19.
  • 6Saldanha-Aranjo F, Ferreira FI, Palma PV, et al. Mesenchymal stromal cells up-regulate CD39 and increase adenosine production to suppress activated T-lymphocytes[ J]. Stem Cell Res, 2011, 7 (1) : 66 -74.
  • 7Del PB, Sportoletti P, Cecchini D, et al. Notchl modulates mesen- chymal stem cells mediated regulatory T-cell induction [ J ]. Eur J Immunol, 2013, 43 ( 1 ) : 182 - 187.
  • 8Ohshima M, Yamahara K, Ishikane S, et al. Systemic transplanta- tion of allogenic fetal membrane-derived mesenchymal stem cells suppresses Thl and Thl7 T cell responses in experimental autoim- mune myocarditis[ J]. J Mol Cell Cardiol, 2012, 53(3) : 420 - 428.
  • 9Suh YG, Kim JK, Byun JS, et al. CDllb: Grl : bone marrow cells ameliorate liver fibrosis by producing interleukin-10 in mice [ J ]. Hepatology, 2012, 56(5): 1902- 1912.
  • 10Wynn TA. Common and unique mechanisms regulate fibrosis in various fibroproliferative diseases [ J ]. J Clin Invest, 2007, 117 (3) : 524 -529.

同被引文献62

引证文献6

二级引证文献24

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部