青光眼
神经退行性变
免疫学
医学
视网膜神经节细胞
正常眼压性青光眼
发病机制
热休克蛋白
自身免疫性疾病
疾病
眼压
视网膜
视网膜
眼科
生物
病理
抗体
开角型青光眼
神经科学
遗传学
基因
标识
DOI:10.1016/j.autrev.2020.102535
摘要
Glaucoma is characterized by retinal ganglion cell (RGC) neurodegeneration. Elevated intraocular pressure (IOP) is a major risk factor however, mechanisms independent of IOP play a role in RGC pathology. Both antibodies and CD4 T-cells as well as microbiota take part in the pathogenesis of both glaucoma and rheumatoid arteritis (RA).Heat shock proteins (HSPs) which originate in bacteria cross-react with RCG epitopes and were involved in rat model of retinal injury. Enhanced expression of HSPs in the retina was associated with glaucoma-like neuropathology and previous studies have also suggested a pathogenic role for HSPs in RA. In view of these data we suggest that glaucoma should be included in the spectrum of autoimmune diseases and that proven medications for RA should be adopted as an innovative IOP -independent therapeutic strategy for glaucoma.
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