Role of immune inflammation regulated by macrophage in the pathogenesis of age-related macular degeneration

被引:1
|
作者
Zhao, Qin [1 ]
Lai, Kunbei [1 ]
机构
[1] Sun Yat Sen Univ, Guangdong Prov Key Lab Ophthalmol & Visual Sci, Guangdong Prov Clin Res Ctr Ocular Dis, State Key Lab Ophthalmol,Zhongshan Ophthalm Ctr, 7 Jinsui Rd, Guangzhou 510060, Peoples R China
基金
中国国家自然科学基金;
关键词
Macrophage; Immune; Inflammation; Age-related macular degeneration; RETINAL-PIGMENT EPITHELIUM; ENDOTHELIAL PROGENITOR CELLS; BRUCHS MEMBRANE IMPLICATIONS; CHOROIDAL NEOVASCULARIZATION; COMPLEMENT ACTIVATION; OXIDATIVE STRESS; GROWTH-FACTOR; RPE CELLS; SUBRETINAL MICROGLIA; GEOGRAPHIC ATROPHY;
D O I
10.1016/j.exer.2023.109770
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Age-related macular degeneration (AMD) can lead to irreversible impairment of visual function, and the number of patients with AMD has been increasing globally. The immunoinflammatory theory is an important pathogenic mechanism of AMD, with macrophages serving as the primary inflammatory infiltrating cells in AMD lesions. Its powerful immunoinflammatory regulatory function has attracted considerable attention. Herein, we provide an overview of the involvement of macrophage-regulated immunoinflammation in different stages of AMD. Additionally, we summarize novel therapeutic approaches for AMD, focusing on targeting macrophages, such as macrophage/microglia modulators, reduction of macrophage aggregation in the subretinal space, modulation of macrophage effector function, macrophage phenotypic alterations, and novel biomimetic nanocomposites development based on macrophage-associated functional properties. We aimed to provide a basis and reference for the further exploration of AMD pathogenesis, developmental influences, and new therapeutic approaches.
引用
收藏
页数:17
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