Department of Ophthalmology, Peking University Third Hospital, Beijing Key Laboratory of Restoration of Damaged Ocular Nerve, Peking University Third Hospital, Haidian District, Beijing, China.
State Key Laboratory of Virology, CAS Center for Excellence in Brain Science and Intelligence Technology, Center for Biosafety Mega-Science, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
Invest Ophthalmol Vis Sci. 2021 Oct 4;62(13):22. doi: 10.1167/iovs.62.13.22.
Considering the difficulty of obtaining adequate biological tissue in clinical practice, we established an animal model of cytomegalovirus (CMV) keratouveitis in rats and investigated the viral infection sites and corresponding imaging and histopathological features.
Subconjunctival injection and topical use of dexamethasone were used to induce ocular immunosuppression in rats followed by intracameral inoculation of murine cytomegalovirus (MCMV). The clinical manifestations, intraocular pressure (IOP) and imaging changes were observed. Infected eyes were further examined by immunofluorescence, light microscopy, and electron microscopy. MCMV RNA was detected by reverse transcription-polymerase chain reaction.
Typical keratouveitis occurred in the experimental rats and was characterized by corneal edema, keratic precipitates, and iridocyclitis with increased IOP. Corneal endothelial lesions displayed as "black holes," enlarged intercellular gaps, and high-intensity cellular infiltration by confocal microscopy, consistent with the pathological changes of "ballooning degeneration," endothelial cell detachment, and inflammatory cell infiltration. Mitochondrial edema was the most prominent organelle lesion in endothelial cells. Trabeculitis, mechanical obstruction of Schlemm's canal, and anterior chamber angle stenosis accounted for elevated IOP. Inflammation of the iris and ciliary body tended to transform into a chronic form. Immunofluorescence revealed that corneal endothelial cells, iris cells, trabecular meshwork cells, and monocytes could be infected by MCMV. MCMV RNA was found in the anterior segments after infection.
CMV can widely infect anterior segment tissue, including the corneal endothelium, iris, and trabecular meshwork, in vivo, inducing the corresponding clinical manifestations. Corneal endotheliitis and hypertensive anterior uveitis could be the specific stage of anterior segment infection of CMV.
考虑到在临床实践中获取足够的生物组织较为困难,我们建立了大鼠巨细胞病毒(CMV)角膜炎动物模型,并研究了病毒感染部位及相应的影像学和组织病理学特征。
通过结膜下注射和局部使用地塞米松诱导大鼠眼免疫抑制,然后向眼内接种鼠巨细胞病毒(MCMV)。观察临床症状、眼内压(IOP)和影像学变化。通过免疫荧光、光镜和电镜进一步检查受感染的眼睛。通过反转录-聚合酶链反应检测 MCMV RNA。
实验大鼠出现典型的角膜炎症,表现为角膜水肿、角膜后沉淀物和虹膜睫状体炎,伴有 IOP 升高。角膜内皮病变表现为“黑洞”、细胞间间隙扩大和高细胞浸润,共焦显微镜检查与“气球样变性”、内皮细胞脱落和炎症细胞浸润的病理变化一致。内皮细胞中最突出的细胞器病变是线粒体水肿。小梁炎、施莱姆氏管机械阻塞和前房角狭窄导致 IOP 升高。虹膜和睫状体的炎症倾向于转变为慢性形式。免疫荧光显示 MCMV 可感染角膜内皮细胞、虹膜细胞、小梁网细胞和单核细胞。感染后在前节发现 MCMV RNA。
CMV 可广泛感染包括角膜内皮、虹膜和小梁网在内的眼前节组织,引起相应的临床表现。角膜内皮炎和高眼压性前葡萄膜炎可能是 CMV 前节感染的特定阶段。