Pumphrey Stephanie A, Pizzirani Stefano, Pirie Christopher G, Anwer M Sawkat, Logvinenko Tanya
Department of Clinical Sciences, Cummings School of Veterinary Medicine, Tufts University, North Grafton, MA 01536, USA.
Am J Vet Res. 2013 Apr;74(4):621-8. doi: 10.2460/ajvr.74.4.621.
To investigate whether differences existed between clinically normal dogs and dogs with goniodysgenesis-related glaucoma (GDRG) in serum autoantibodies against optic nerve antigens.
16 dogs with GDRG, 17 healthy dogs with unremarkable pectinate ligament and iridocorneal angle morphology, and 13 euthanized dogs with no major ocular abnormalities or underlying diseases.
Western blotting was performed with optic nerve extracts from the euthanized dogs as an antigen source and serum from clinically normal dogs and dogs with GDRG as a primary antibody (autoantibody) source. Blots were evaluated for presence and density of bands.
Multiple bands were identified on western blots from all dogs with GDRG and all clinically normal dogs, with a high degree of variability among individual dogs. Dogs with GDRG were significantly more likely than healthy dogs to have bands present at 38, 40, and 68 kDa. Dogs with GDRG had significant increases in autoreactivity at 40 and 53 kDa and a significant decrease in autoreactivity at 48 kDa.
Significant differences in serum autoantibodies against optic nerve antigens were found in dogs with versus without GDRG. Although it remains unclear whether these differences were part of the pathogenesis of disease or were sequelae to glaucomatous changes, these findings provide support for the hypothesis that immune-mediated mechanisms play a role in the development or progression of GDRG. However, the high degree of variability among individual dogs and the considerable overlap between groups suggest that the clinical usefulness of this technique for distinguishing dogs with GDRG from clinically normal dogs is likely limited.
研究临床正常犬与患有与前房角发育异常相关青光眼(GDRG)的犬在针对视神经抗原的血清自身抗体方面是否存在差异。
16只患有GDRG的犬、17只梳状韧带和虹膜角膜角形态正常的健康犬以及13只无主要眼部异常或潜在疾病的安乐死犬。
以安乐死犬的视神经提取物作为抗原来源,以临床正常犬和患有GDRG的犬的血清作为一抗(自身抗体)来源进行蛋白质印迹法检测。评估印迹上条带的存在情况和密度。
在所有患有GDRG的犬和所有临床正常犬的蛋白质印迹上均鉴定出多条条带,个体犬之间存在高度变异性。患有GDRG的犬比健康犬更有可能在38 kDa、40 kDa和68 kDa处出现条带。患有GDRG的犬在40 kDa和53 kDa处的自身反应性显著增加,在48 kDa处的自身反应性显著降低。
在患有和未患有GDRG的犬中发现了针对视神经抗原的血清自身抗体存在显著差异。尽管尚不清楚这些差异是疾病发病机制的一部分还是青光眼性改变的后遗症,但这些发现为免疫介导机制在GDRG的发生或发展中起作用这一假说提供了支持。然而,个体犬之间的高度变异性以及组间相当大的重叠表明,该技术用于区分患有GDRG的犬与临床正常犬的临床实用性可能有限。