Delbosc B, Fellmann D, Piquot X, Montard M, Royer J
Clinique ophtalmologique, CHU Jean-Minjoz, Besançon.
J Fr Ophtalmol. 1990;13(11-12):535-41.
Fresh human corneas and corneal buttons were studied for expression of HLA antigens. Using monoclonal antibodies in an indirect immunofluorescence assay, corneal layers were examined for class I (HLA-A, B, C) and class II (HLA-DR) histocompatibility antigens. Twenty-one human corneas were studied, 6 normal and 15 pathological: 4 buttons of allograft rejection, 9 buttons of pseudophakic bullous keratopathy. In fresh control corneas, HLA-A, B, C antigens were localized on corneal epithelium and on stromal keratocytes but were never found on endothelial cells. HLA-DR antigens were not detected on corneal epithelium, stroma or endothelium but were detected on Langerhans cells within epithelium and anterior stroma. At the corneal limbus, HLA class I-II antigens were expressed on vascular endothelium. HLA antigen distribution was modified in pathological corneas. Antigens HLA-A, B, C were induced on endothelial cells of rejected corneal allografts. Antigens HLA-DR were detected on epithelial cells, cells in the stroma of pseudophakic bullous keratopathy and also on endothelial cells of rejected corneal allografts. These results suggest that induction of class I and II antigen expression by inflammatory factors may occur in vivo. In rejected corneal allografts induction of HLA-DR antigen on corneal layers would intensify the process of rejection. This study and others have demonstrated the ability of modulation of HLA antigen expression on human corneal cells in vivo.
对新鲜的人角膜和角膜植片进行了HLA抗原表达的研究。在间接免疫荧光测定中使用单克隆抗体,检测角膜各层的I类(HLA - A、B、C)和II类(HLA - DR)组织相容性抗原。共研究了21个人角膜,其中6个正常角膜和15个病理角膜:4个同种异体移植排斥的植片,9个假晶状体大泡性角膜病变的植片。在新鲜对照角膜中,HLA - A、B、C抗原定位于角膜上皮和基质角膜细胞,但从未在内皮细胞中发现。在角膜上皮、基质或内皮细胞上未检测到HLA - DR抗原,但在上皮和前基质内的朗格汉斯细胞上检测到。在角膜缘,HLA I - II类抗原在血管内皮上表达。在病理角膜中HLA抗原分布发生改变。在排斥的角膜同种异体移植的内皮细胞上诱导出HLA - A、B、C抗原。在假晶状体大泡性角膜病变的上皮细胞、基质细胞以及排斥的角膜同种异体移植的内皮细胞上检测到HLA - DR抗原。这些结果表明炎症因子可能在体内诱导I类和II类抗原表达。在排斥的角膜同种异体移植中,角膜各层上HLA - DR抗原的诱导会加剧排斥过程。本研究及其他研究已证明在体内可调节人角膜细胞上HLA抗原的表达。