Gaweco A S, Wiesner R H, Yong S, Krom R, Porayko M, Chejfec G, McClatchey K D, Van Thiel D H
Liver Transplant Program, Loyola University Medical Center, Maywood, IL 60153, USA.
Liver Transpl Surg. 1999 Jan;5(1):1-7. doi: 10.1002/lt.500050108.
The CD40-CD40L (CD154) interaction plays a pivotal role in the effector mechanisms of allograft rejection. Blockade of the CD40/CD40L costimulatory pathway prevents the development of chronic allograft rejection in several animal transplant models. The relevance of in situ CD40 and CD40L expression in human liver allografts was assessed by immunohistochemistry during ductopenic chronic rejection (CR). In CR allograft specimens (n = 8), marked CD40L expression was detected on Kupffer cells (KCs) and sinusoidal macrophages with a unique centrilobular distribution (P <.001). The CD40L+ KCs and macrophages were shown to be CD68+ after immunohistochemical analysis of serial sections with anti-CD68 monoclonal antibody. Moderate staining of vascular and sinusoidal endothelial cells and mononuclear infiltrates was observed in some CR cases. These findings were in contrast to the absence of CD40L expression in controls (n = 11) consisting of stable liver allograft and normal liver tissue specimens. Only occasional CD40 expression in some cases of CR and controls was observed. In CR, CD40L (CD154) expression is manifested on KCs and macrophages. The present novel data show another important cellular source of CD40L expression and suggest a potential role of KCs/macrophages and CD40/CD40L costimulatory interactions in the pathogenesis of chronic rejection ductopenic liver allograft.
CD40-CD40L(CD154)相互作用在同种异体移植排斥反应的效应机制中起关键作用。在多种动物移植模型中,阻断CD40/CD40L共刺激途径可预防慢性同种异体移植排斥反应的发生。通过免疫组织化学方法评估了在胆管缺失性慢性排斥反应(CR)期间人肝同种异体移植中原位CD40和CD40L的表达情况。在CR同种异体移植标本(n = 8)中,在库普弗细胞(KC)和具有独特小叶中心分布的窦状巨噬细胞上检测到明显的CD40L表达(P <.001)。在用抗CD68单克隆抗体对连续切片进行免疫组织化学分析后,显示CD40L+ KC和巨噬细胞为CD68+。在一些CR病例中观察到血管和窦状内皮细胞及单核浸润的中度染色。这些发现与由稳定肝同种异体移植和正常肝组织标本组成的对照组(n = 11)中缺乏CD40L表达形成对比。在CR和对照组的一些病例中仅偶尔观察到CD40表达。在CR中,CD40L(CD154)表达表现在KC和巨噬细胞上。目前的新数据显示了CD40L表达的另一个重要细胞来源,并提示KC/巨噬细胞和CD40/CD40L共刺激相互作用在慢性排斥性胆管缺失性肝同种异体移植发病机制中的潜在作用。