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Strong additive effect of calcitriol and cyclosporine A on lymphocyte proliferation in vitro and rat liver allotransplantations in vivo 被引量:6

Strong additive effect of calcitriol and cyclosporine A on lymphocyte proliferation in vitro and rat liver allotransplantations in vivo
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摘要 Background Vitamin D3 and its metabolites have been found to exert immunosuppressive effects both in vivo and in vitro. We investigated the synergistic effect of calcitriol and cyclosporine A (CsA) on lymphocyte proliferation in vitro and graft rejection following rat liver allotransplantations in vivo. Methods Alloantigen driven, human peripheral mononuclear cells' proliferation and cytokine production capacity were tested in the presence or absence of various concentrations of calcitriol or CsA. In vivo, liver allografts were transplanted in a high responder strain combination (SD to Wistar) rats and combination of subtherapeutical dose of CsA and calcitriol was administered in recipients, whereas the control recipients received single or no immunosuppressant. Proliferation of splenocyte from recipient was tested with mixed lymphocyte reaction. Serum intedeukin-2 (IL-2) and interferon gamma (IFN-γ) concentrations were measured with enzyme linked immunosorbent assay. Results Combined medication of 10^-9 mol/L calcitriol and 100 ng/ml CsA inhibited human peripheral mononuclear cells' proliferation to alloantigen and the production of IL-2 and IFN-γ but promoted that of IL-4 and IL-10. Similarly, combination of 250 ng · kg^-1·-d^-1 calcitriol and 1.0 mg · kg^-1·-d^-1 CsA showed an additive effect in liver transplant model. It restrained splenocyte proliferation to alloantigen from donor and significantly reduced serum concentration of IL-2 and IFN-γ in recipients. Consequently, aUograft rejection in combined medication group was minor (median William's grade was 1.0 vs 3.0 in combined medication group and in the control group, P〈0.05) and the recipients' survival was evidently prolonged [(93.7±5.8) days vs (12.6±1.4) days in combined medication group and in the control group, P〈0.01 ]. Conclusion A combination of calcitriol and CsA has an additive effect on limiting lymphocyte proliferation and prolonging liver graft survival. With its additional immunomodulating property, calcitriol is a potent immunosuppressant that can extend the therapeutic window of classical immunomodulators in prevention and treatment of liver graft rejection. Background Vitamin D3 and its metabolites have been found to exert immunosuppressive effects both in vivo and in vitro. We investigated the synergistic effect of calcitriol and cyclosporine A (CsA) on lymphocyte proliferation in vitro and graft rejection following rat liver allotransplantations in vivo. Methods Alloantigen driven, human peripheral mononuclear cells' proliferation and cytokine production capacity were tested in the presence or absence of various concentrations of calcitriol or CsA. In vivo, liver allografts were transplanted in a high responder strain combination (SD to Wistar) rats and combination of subtherapeutical dose of CsA and calcitriol was administered in recipients, whereas the control recipients received single or no immunosuppressant. Proliferation of splenocyte from recipient was tested with mixed lymphocyte reaction. Serum intedeukin-2 (IL-2) and interferon gamma (IFN-γ) concentrations were measured with enzyme linked immunosorbent assay. Results Combined medication of 10^-9 mol/L calcitriol and 100 ng/ml CsA inhibited human peripheral mononuclear cells' proliferation to alloantigen and the production of IL-2 and IFN-γ but promoted that of IL-4 and IL-10. Similarly, combination of 250 ng · kg^-1·-d^-1 calcitriol and 1.0 mg · kg^-1·-d^-1 CsA showed an additive effect in liver transplant model. It restrained splenocyte proliferation to alloantigen from donor and significantly reduced serum concentration of IL-2 and IFN-γ in recipients. Consequently, aUograft rejection in combined medication group was minor (median William's grade was 1.0 vs 3.0 in combined medication group and in the control group, P〈0.05) and the recipients' survival was evidently prolonged [(93.7±5.8) days vs (12.6±1.4) days in combined medication group and in the control group, P〈0.01 ]. Conclusion A combination of calcitriol and CsA has an additive effect on limiting lymphocyte proliferation and prolonging liver graft survival. With its additional immunomodulating property, calcitriol is a potent immunosuppressant that can extend the therapeutic window of classical immunomodulators in prevention and treatment of liver graft rejection.
出处 《Chinese Medical Journal》 SCIE CAS CSCD 2006年第24期2090-2095,共6页 中华医学杂志(英文版)
基金 ThestudywassupportedbyagrantfromtheNationalBasicResearchProgram(973Program)ofChina(2003CB515501).
关键词 liver transplantation vitamin D CYCLOSPORINE CYTOKINE LYMPHOCYTE graft rejection liver transplantation vitamin D cyclosporine cytokine lymphocyte graft rejection
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  • 1Kiani A,Garcia-Cozar FJ,Habermann I,Laforsch S,Aebischer T,Ehninger G,et al.Regulation of interferon-gamma gene expression by nuclear factor of activated T cells[].Blood.2001
  • 2Jiang S,Herrera O,Lechler RI.New spectrum of allorecognition pathways: implications for graft rejection and transplantation tolerance[].Current Opinion in Immunology.2004
  • 3Williams JW,Peters TG,Vera SR,Britt LG,van Voorst SJ,Haggitt RC.Biopsy directed immunosuppression following hepatic transplantation[].Transplantation.1985
  • 4Serfling E,Berberich-Siebelt F,Avots A,Chuvpilo S,Klein-Hessling S,Jha MK,et al.NFAT and NF-kappaB factors-the distant relatives[].International Journal of Biochemistry Cell Biology The.2004
  • 5Takeuchi A,Reddy GS,Kobayashi T,Okano T,Park J,Sharma S.Nuclear factor of activated T cells (NFAT) as a molecular target for 1alpha,25-dihydroxyvitamin D3-mediated effects[].J Immunol.1998
  • 6Matsuda S,Koyasu S.Mechanisms of action of cyclosporine[].Immunopharmacology.2000
  • 7Venkatesh N,Feng Y,DeDecker B,Yacono P,Golan D,Mitchison T,et al.Chemical genetics to identify NFAT inhibitors: potential of targeting calcium mobilization in immunosuppression[].Proceedings of the National Academy of Sciences of the United States of America.2004
  • 8Hullett DA,Laeseke PF,Malin G,Nessel R,Sollinger HW,Becker BN.Prevention of chronic allograft nephropathy with vitamin D[].Transplant International.2005
  • 9Penna G,Roncari A,Amuchastegui S,Daniel KC,Berti E,Colonna M,et al.Expression of the inhibitory receptor ILT3 on dendritic cells is dispensable for induction of CD4+Foxp3+ regulatory T cells by 1,25-dihydroxyvitamin D3[].Blood.2005
  • 10Giarratana N,Penna G,Amuchastegui S,Mariani R,Daniel KC,Adorini L.A vitamin D analog down-regulates proinflammatory chemokine production by pancreatic islets inhibiting T cell recruitment and type 1 diabetes development[].J Immunol.2004

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