Grus Franz H, Joachim Stephanie C, Hoffmann Esther M, Pfeiffer Norbert
Universitaets-Augenklinik, Department of Ophthalmology, University of Mainz, Mainz, Germany.
Mol Vis. 2004 Feb 25;10:132-7.
Glaucoma is one of the leading causes for blindness in the world. It is characterized by a progressive loss of retinal ganglion cells. An elevated intraocular pressure cannot explain the disease in all subjects. Autoimmune mechanisms maybe involvemed in the pathogenesis of the disease. The aim of our study was to analyze the IgG autoantibody repertoires in sera of glaucomatous subjects against optic nerve antigens.
Ninety-four subjects were included in this comparative cross-sectional study of healthy (CTRL), primary-open-angle-glaucoma (POAG), ocular-hypertension (OHT), and normal-tension-glaucoma (NTG) volunteers. Sera of subjects were tested against western blots of optic nerve antigens. For each western blot, a densitograph was built by digital image analysis and subsequently a multivariate analysis of discriminance was performed.
Complex IgG autoantibody repertoires could be found in all subjects, even in healthy subjects. The multivariate analysis of discriminance can test for statistical differences between the groups using the whole complex staining pattern for the calculation. A significant difference between all groups against optic nerve antigens was found. The NTG group had the highest variance from controls (p<0.01).
This study demonstrates immunological effects in POAG and NTG and may provide further evidence for an involvement of autoantibodies in the pathogenesis of both NTG and POAG. Using the techniques presented in this study, the differences in the complex autoantibody repertoires were assessed by means of statistical analysis. Further studies are needed to determine whether these changes in autoantibodies could be helpful in the diagnosis of glaucoma.
青光眼是全球主要致盲原因之一。其特征为视网膜神经节细胞进行性丧失。眼内压升高并不能解释所有患者的病情。自身免疫机制可能参与了该疾病的发病过程。我们研究的目的是分析青光眼患者血清中针对视神经抗原的IgG自身抗体谱。
本比较性横断面研究纳入了94名健康(CTRL)、原发性开角型青光眼(POAG)、高眼压症(OHT)和正常眼压性青光眼(NTG)志愿者。检测受试者血清对视神经抗原的免疫印迹反应。对于每次免疫印迹,通过数字图像分析构建密度图,随后进行判别多元分析。
在所有受试者中,甚至在健康受试者中,均可发现复杂的IgG自身抗体谱。判别多元分析可利用整个复杂染色模式进行计算,以检测各组之间的统计学差异。发现所有组对视神经抗原均存在显著差异。NTG组与对照组的差异最大(p<0.01)。
本研究证明了POAG和NTG中的免疫效应,并可能为自身抗体参与NTG和POAG发病机制提供进一步证据。利用本研究中介绍的技术,通过统计分析评估了复杂自身抗体谱的差异。需要进一步研究以确定这些自身抗体的变化是否有助于青光眼的诊断。