Rodrigo Maria J, Subías Manuel, Montolío Alberto, Martínez-Rincón Teresa, Aragón-Navas Alba, Bravo-Osuna Irene, Pablo Luis E, Cegoñino Jose, Herrero-Vanrell Rocío, Garcia-Martin Elena, Pérez Del Palomar Amaya
Department of Ophthalmology, Miguel Servet University Hospital, 50009 Zaragoza, Spain.
Miguel Servet Ophthalmology Research Group (GIMSO), Aragon Health Research Institute (IIS Aragon), University of Zaragoza, 50009 Zaragoza, Spain.
Biomedicines. 2024 Mar 13;12(3):633. doi: 10.3390/biomedicines12030633.
Glaucoma is a multifactorial pathology involving the immune system. The subclinical immune response plays a homeostatic role in healthy situations, but in pathological situations, it produces imbalances. Optical coherence tomography detects immune cells in the vitreous as hyperreflective opacities and these are subsequently characterised by computational analysis. This study monitors the changes in immunity in the vitreous in two steroid-induced glaucoma (SIG) animal models created with drug delivery systems (microspheres loaded with dexamethasone and dexamethasone/fibronectin), comparing both sexes and healthy controls over six months. SIG eyes tended to present greater intensity and a higher number of vitreous opacities ( < 0.05), with dynamic fluctuations in the percentage of isolated cells (10 µm), non-activated cells (10-50 µm), activated cells (50-250 µm) and cell complexes (>250 µm). Both SIG models presented an anti-inflammatory profile, with non-activated cells being the largest population in this study. However, smaller opacities (isolated cells) seemed to be the first responder to noxa since they were the most rounded (recruitment), coinciding with peak intraocular pressure increase, and showed the highest mean Intensity (intracellular machinery), even in the contralateral eye, and a major change in orientation (motility). Studying the features of hyperreflective opacities in the vitreous using OCT could be a useful biomarker of glaucoma.
青光眼是一种涉及免疫系统的多因素病理学疾病。亚临床免疫反应在健康状态下发挥着稳态作用,但在病理状态下,它会导致失衡。光学相干断层扫描将玻璃体中的免疫细胞检测为高反射性混浊物,随后通过计算分析对这些混浊物进行表征。本研究监测了两种使用药物递送系统(载有地塞米松和地塞米松/纤连蛋白的微球)创建的类固醇诱导性青光眼(SIG)动物模型中玻璃体免疫的变化,比较了六个月内的两性和健康对照。SIG眼往往呈现出更高的强度和更多的玻璃体混浊物(<0.05),分离细胞(10 µm)、未激活细胞(10 - 50 µm)、激活细胞(50 - 250 µm)和细胞复合体(>250 µm)的百分比存在动态波动。两种SIG模型均呈现出抗炎特征,未激活细胞是本研究中数量最多的群体。然而,较小的混浊物(分离细胞)似乎是对损伤的第一反应者,因为它们最圆润(募集),这与眼内压升高的峰值同时出现,并且即使在对侧眼中也显示出最高的平均强度(细胞内机制)以及方向的重大变化(运动性)。使用光学相干断层扫描研究玻璃体中高反射性混浊物的特征可能是青光眼的一种有用生物标志物。