Maruyama Takahiro, Jaramillo Andrés, Narayanan Kishore, Higuchi Toru, Mohanakumar T
Department of Surgery, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Am J Transplant. 2005 Sep;5(9):2126-34. doi: 10.1111/j.1600-6143.2005.00999.x.
Anti-HLA class I Abs are associated with the development of bronchiolitis obliterans syndrome (BOS) after lung transplantation. BOS is characterized histologically by fibrosis and airway epithelial cell apoptosis. We have previously shown that anti-HLA class I Abs induce proliferation, growth factor production and apoptosis in airway epithelial cells in vitro. Thus, this study was designed to determine whether anti-HLA class I Abs alone could induce obliterative airway disease (OAD) in heterotopic murine tracheal allografts. Toward this, HLA-A*0201-transgenic tracheal allografts were transplanted into Rag1-deficient mice treated with the W6/32 anti-HLA class I mAb. Allografts were harvested at days +30, +45, +60 and +90. Allografts displayed epithelial metaplasia by day +45, epithelial destruction and mild cellular infiltration by day +60 and complete lumen obliteration and moderate cellular infiltration by day +90. Anti-HLA class I Abs induced the production of several growth factors and growth factor receptors and apoptosis of parenchymal cells in the allograft. In addition, anti-HLA class I Abs induced macrophages and granulocytes infiltration. The results from this study demonstrate that anti-HLA class I Abs play an important role in the pathogenesis of OAD by inducing growth factor production, apoptosis and chemotaxis of inflammatory cells.
抗HLA I类抗体与肺移植后闭塞性细支气管炎综合征(BOS)的发生有关。BOS的组织学特征为纤维化和气道上皮细胞凋亡。我们之前已经表明,抗HLA I类抗体在体外可诱导气道上皮细胞增殖、生长因子产生和凋亡。因此,本研究旨在确定单独的抗HLA I类抗体是否能在异位小鼠气管同种异体移植中诱导闭塞性气道疾病(OAD)。为此,将HLA-A*0201转基因气管同种异体移植物移植到用W6/32抗HLA I类单克隆抗体处理的Rag1缺陷小鼠体内。在第30天、第45天、第60天和第90天收获同种异体移植物。到第45天时,同种异体移植物出现上皮化生,到第60天时出现上皮破坏和轻度细胞浸润,到第90天时出现管腔完全闭塞和中度细胞浸润。抗HLA I类抗体诱导同种异体移植物中几种生长因子和生长因子受体的产生以及实质细胞的凋亡。此外,抗HLA I类抗体诱导巨噬细胞和粒细胞浸润。本研究结果表明,抗HLA I类抗体通过诱导生长因子产生、细胞凋亡和炎性细胞趋化作用在OAD的发病机制中起重要作用。