IMED AB, 171 65 Solna, Sweden.
Transplantation. 2011 May 15;91(9):946-51. doi: 10.1097/TP.0b013e318212c833.
Graft-versus-host disease (GVHD) is an important complication occurring after hematopoietic stem-cell transplantation (HSCT). Animal model studies have shown the involvement of the Fas (APO-1/CD95)/Fas-Ligand pathway in GVHD pathogenesis, but its association with cutaneous GVHD in human remains to be established.
In the present study, Fas involvement in skin damage was assessed using a human skin explant model of GVHD. Fas and FasL expression were measured by immunohistochemistry and blockade of Fas pathway was investigated using an antagonistic anti-human Fas monoclonal antibody. In addition, levels of soluble Fas (sFas) were determined in the serum of patients receiving allogeneic HSCT with and without GVHD.
The results showed that Fas up-regulation in the epithelium of human skin explants correlated with graft-versus-host reaction (GVHR) in the skin explant model (P<0.001). Decreased GVHR grades were observed by using a Fas blocking monoclonal antibody. Levels of sFas were increased post-HSCT (P<0.001) but rather than being associated with the severity of GVHD, sFas levels differed with the conditioning treatments the patients received before the HSCT.
Higher GVHR grades were associated with increased Fas expression in the epithelium of the skin explants. In addition, by blocking Fas-mediated apoptosis, the GVHR grades were decreased. Our study thus shows the involvement of Fas in cutaneous GVHD damage, and supports the potential use of Fas as a therapeutic target.
移植物抗宿主病(GVHD)是造血干细胞移植(HSCT)后发生的一种重要并发症。动物模型研究表明,Fas(APO-1/CD95)/Fas 配体途径参与 GVHD 的发病机制,但在人类中与皮肤 GVHD 的关联尚未确定。
在本研究中,使用人皮肤 GVHD 体外模型评估 Fas 在皮肤损伤中的作用。通过免疫组织化学测定 Fas 和 FasL 的表达,并使用拮抗抗人 Fas 单克隆抗体研究 Fas 途径的阻断。此外,还测定了接受异基因 HSCT 且有或无 GVHD 的患者血清中的可溶性 Fas(sFas)水平。
结果表明,人皮肤外植体中 Fas 的上调与皮肤外植体模型中的移植物抗宿主反应(GVHR)相关(P<0.001)。使用 Fas 阻断单克隆抗体观察到 GVHR 分级降低。HSCT 后 sFas 水平升高(P<0.001),但与 GVHD 的严重程度无关,sFas 水平因患者在 HSCT 前接受的调理治疗而异。
较高的 GVHR 分级与皮肤外植体上皮中 Fas 表达增加相关。此外,通过阻断 Fas 介导的细胞凋亡,GVHR 分级降低。因此,我们的研究表明 Fas 参与皮肤 GVHD 损伤,并支持 Fas 作为治疗靶点的潜力。