期刊文献+

Immunological tolerance of human hepatocyte xenograft induced by adenovirus vector-mediated CTLA4Ig gene transfer 被引量:2

Immunological tolerance of human hepatocyte xenograft induced by adenovirus vector-mediated CTLA4Ig gene transfer
下载PDF
导出
摘要 BACKGROUND:Systemic administration of CTLA4Ig has been applied in inducing immunological tolerance of hepatocyte implants,but has potential for systemic immune inhibition.This study was designed to induce hepatocyte immunological tolerance by locally expressing CTLA4Ig in an attempt to improve the effectiveness of cell transplantation.METHODS:A normal human liver cell line(L02) was transfected with adenovirus vector containing the CTLA4Ig gene(Ad-CTLA4Ig-EGFP) in vitro,and the expression of CTLA4Ig by transfected cells was assessed by fluorescent imaging and immunocytochemical staining.Transfected cells then were injected into the spleen of Sprague-Dawley rats,the survival of cells was determined by immunohistochemistry,and the immune status was examined through CD4 + and CD69 + T cellcounts and ELISA detection of IL-2 in peripheral blood.RESULTS:L02 cells expressed CTLA4Ig in the cytoplasm for >4 weeks.Surviving L02 cells were observed in the experimental group at 3 and 4 weeks post-transplantation,while none was detected in the control group.Furthermore,the percentages of CD4 + and CD4 + CD69 + T cells in the CTLA4-transfected group were 24.5% and 45.1%,markedly lower than those in the control group at 4 weeks post-transplantation(P<0.01).Furthermore,the IL-2 level was also lower in the CTLA4transfected group than in the control group.CONCLUSION:Adenovirus-mediated CTLA4Ig gene transfer into human hepatocytes has the potential to become an effective method of inducing immunological tolerance in hepatocyte transplantation. BACKGROUND:Systemic administration of CTLA4Ig has been applied in inducing immunological tolerance of hepatocyte implants,but has potential for systemic immune inhibition.This study was designed to induce hepatocyte immunological tolerance by locally expressing CTLA4Ig in an attempt to improve the effectiveness of cell transplantation.METHODS:A normal human liver cell line(L02) was transfected with adenovirus vector containing the CTLA4Ig gene(Ad-CTLA4Ig-EGFP) in vitro,and the expression of CTLA4Ig by transfected cells was assessed by fluorescent imaging and immunocytochemical staining.Transfected cells then were injected into the spleen of Sprague-Dawley rats,the survival of cells was determined by immunohistochemistry,and the immune status was examined through CD4 + and CD69 + T cellcounts and ELISA detection of IL-2 in peripheral blood.RESULTS:L02 cells expressed CTLA4Ig in the cytoplasm for >4 weeks.Surviving L02 cells were observed in the experimental group at 3 and 4 weeks post-transplantation,while none was detected in the control group.Furthermore,the percentages of CD4 + and CD4 + CD69 + T cells in the CTLA4-transfected group were 24.5% and 45.1%,markedly lower than those in the control group at 4 weeks post-transplantation(P<0.01).Furthermore,the IL-2 level was also lower in the CTLA4transfected group than in the control group.CONCLUSION:Adenovirus-mediated CTLA4Ig gene transfer into human hepatocytes has the potential to become an effective method of inducing immunological tolerance in hepatocyte transplantation.
出处 《Hepatobiliary & Pancreatic Diseases International》 SCIE CAS 2012年第2期148-153,共6页 国际肝胆胰疾病杂志(英文版)
基金 supported by a grant from the National Basic Research of China(973 Program 2007CB512903)
关键词 CTLA4IG adenovirus vectors hepatocyte transplantation immune tolerance graft rejection CTLA4Ig adenovirus vectors hepatocyte transplantation immune tolerance graft rejection
  • 相关文献

参考文献28

  • 1Alegre ML,Fallarino F.Mechanisms of CTLA-4-Ig in tolerance induction. Current Pharmaceutical Design . 2006 被引量:1
  • 2Collins AV,Brodie DW,Gilbert RJ,Iaboni A,Manso-SanchoR,Walse B,et al.The interaction properties of costimulatory molecules revisited. Immunity . 2002 被引量:1
  • 3Ikemizu S,Gilbert RJ,Fennelly JA,Collins AV,Harlos K,Jones EY,et al.Structure and dimerization of a soluble formof B7-1. Immunity . 2000 被引量:1
  • 4Potiron N,Chagneau C,Boeffard F,Soulillou JP,Anegon I,Le Mauff B.Adenovirus-mediated CTLA4Ig or CD40Ig gene transfer delays pancreatic islet rejection in a rat-to-mouse xenotransplantation model after systemic but not local expression. Cell Transplantation . 2005 被引量:1
  • 5Gause W C,Halvorson M J,Lu P,et al.The function of costimulatory molecules and the development of IL-4-producing T cells. Immunology Today . 1997 被引量:1
  • 6Linsley P S;Wallace P M;Johnson J.Immunosuppression in vivo by a soluble form of the CTLA-4 T cell activation molecule,1992(5071). 被引量:1
  • 7Guha C,Deb N J,Sappal B S,et al.Amplification of engrafted hepatocytes by preparative manipulation of the host liver. Artificial Organs . 2001 被引量:1
  • 8Hirakawa E,Yasunami Y,Nakano M,et al.Amelioration of hyperglycemia in streptozotocin-induced diabetic mice with fetal pancreatic allografts: prevention of rejection by donor specific transfusion in conjunction with CTLA4Ig. Pancreas . 2004 被引量:1
  • 9Harper K,Balzano C,Rouvier E,et al.CTLA-4 and CD28 activated lymphocyte molecules are closely related in both mouse and human as to sequence, message expression, gene structure, and chromosomal location. Journal of Immunology . 1991 被引量:1
  • 10Stamper C C,Zhang Y,Tobin J F,et al.Crystal structure of the B7-1/CTLA-4 complex that inhibits human immune responses. Nature . 2001 被引量:1

共引文献2

同被引文献6

引证文献2

二级引证文献5

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