Csencsits K, Wood S C, Lu G, Faust S M, Brigstock D, Eichwald E J, Orosz C G, Bishop D K
Section of General Surgery, Department of Surgery, University of Michigan School of Medicine, Ann Arbor, MI 48109, USA.
Am J Transplant. 2006 May;6(5 Pt 1):959-66. doi: 10.1111/j.1600-6143.2006.01292.x.
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.
移植器官功能的晚期丧失主要归因于慢性排斥反应(CR)。目前尚无针对CR的有效治疗方法,且该疾病的潜在病因尚不清楚。本研究比较了接受抗CD4治疗并发生CR的小鼠与接受抗CD40L治疗且未发生CR的小鼠体内心脏移植器官内发生的事件。转化生长因子β(TGFβ)和由TGFβ诱导产生的结缔组织生长因子(CTGF)在发生CR的移植器官中均有表达,但在未发生CR的移植器官中不表达。在接受抗CD40L治疗的受体中,对移植器官进行TGFβ转染会导致CTGF表达及CR。然而,对同基因移植器官进行TGFβ转染并不会导致CTGF表达或CR。这些数据表明,单独的TGFβ不足以诱导CR,CTGF是必需的。此外,TGFβ诱导CTGF需要抗原刺激。因此,CTGF可能成为CR的治疗靶点。