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Am J Transplant ; 6(5 Pt 1): 959-66, 2006 May.
Article in English | MEDLINE | ID: mdl-16611331

ABSTRACT

Late loss of allograft function is primarily attributed to chronic rejection (CR). There are no effective treatments for CR and the underlying cause of the disease is unknown. This study compared events that occurred within cardiac allografts placed in mice that received either anti-CD4 therapy and develop CR or anti-CD40L therapy and do not develop CR. Both TGFbeta and connective tissue growth factor (CTGF), which is induced by TGFbeta, were expressed in grafts with CR but were not expressed in grafts without CR. TGFbeta transfection of allografts in anti-CD40L-treated recipients resulted in CTGF expression and CR. However, TGFbeta transfection of syngeneic grafts did not result in CTGF expression or CR. These data indicate that TGFbeta alone is insufficient to induce CR and that CTGF is required. Further, antigenic stimulation is required for TGFbeta induction of CTGF. Thus, CTGF may serve as a therapeutic target for CR.


Subject(s)
Graft Rejection/pathology , Heart Transplantation/immunology , Immediate-Early Proteins/physiology , Intercellular Signaling Peptides and Proteins/physiology , Transforming Growth Factor beta/physiology , Animals , CD40 Ligand/immunology , Connective Tissue Growth Factor , Female , Heart Transplantation/pathology , Immediate-Early Proteins/genetics , Immediate-Early Proteins/immunology , Immunohistochemistry , Intercellular Signaling Peptides and Proteins/genetics , Intercellular Signaling Peptides and Proteins/immunology , Male , Mice , Mice, Inbred BALB C , Mice, Inbred C57BL , Transfection , Transforming Growth Factor beta/immunology , Transplantation, Homologous , Transplantation, Isogeneic
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