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Published on: June 17, 2020
Relationship between choroidal thickness changes and macrophage polarization in high myopia
Zhou Zhou1, Wen Long2, Bingru Zheng2
1The Second Clinical Medical College of Jinan University, Shenzhen Eye Hospital, Shenzhen, China.
Frontiers in Medicine
|May 8, 2026
Summary
High myopia causes blindness through progressive choroidal thinning. This thinning involves immune cells, specifically macrophages, driving destructive remodeling, suggesting new therapeutic targets for myopia.
Area of Science:
- Ophthalmology
- Immunology
- Pathology
Background:
- High myopia is a leading cause of global blindness, characterized by progressive choroidal thinning.
- Traditional theories attribute choroidal thinning to mechanical stretch or reduced blood flow.
- Emerging evidence points to active immune-inflammatory processes in the choroid.
Purpose of the Study:
- To review recent findings in myopia and immunology.
- To propose a pathological framework for high myopia involving immune-inflammatory remodeling.
- To explore the role of macrophage polarization in choroidal degeneration.
Main Methods:
- Systematic review of myopia and immunology literature.
- Integration of clinical imaging, intraocular fluid analysis, and animal experimental data.
- Focus on the sequence: mechanical stretch/hypoxia-immune imbalance-macrophage polarization-choroidal remodeling.
Main Results:
- Proposed framework: mechanical stretch/hypoxia induces immune imbalance, leading to macrophage polarization and destructive choroidal remodeling.
- Macrophages, upon sensing stress, contribute to choroidal degeneration via cytokine release, matrix metabolism changes, and vascular regression.
- Identified gaps in human tissue data and macrophage subset-specific interventions.
Conclusions:
- Immune-inflammatory processes, particularly macrophage polarization, are central to high myopia pathogenesis.
- Understanding these mechanisms offers potential for novel prevention and treatment strategies.
- Future research should focus on human data, specific macrophage interventions, spatial transcriptomics, and immune modulation.