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年龄相关性黄斑变性的免疫学。

Immunology of age-related macular degeneration.

机构信息

Department of Ophthalmology and Visual Sciences, University of Kentucky, Lexington, Kentucky 40506, USA.

出版信息

Nat Rev Immunol. 2013 Jun;13(6):438-51. doi: 10.1038/nri3459.

DOI:10.1038/nri3459
PMID:23702979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3941009/
Abstract

Age-related macular degeneration (AMD) is a leading cause of blindness in aged individuals. Recent advances have highlighted the essential role of immune processes in the development, progression and treatment of AMD. In this Review we discuss recent discoveries related to the immunological aspects of AMD pathogenesis. We outline the diverse immune cell types, inflammatory activators and pathways that are involved. Finally, we discuss the future of inflammation-directed therapeutics to treat AMD in the growing aged population.

摘要

年龄相关性黄斑变性(AMD)是老年人致盲的主要原因。最近的研究进展强调了免疫过程在 AMD 发病机制中的发展、进展和治疗中的重要作用。在这篇综述中,我们讨论了与 AMD 发病机制的免疫学方面相关的最新发现。我们概述了涉及的不同免疫细胞类型、炎症激活物和途径。最后,我们讨论了针对 AMD 进行炎症靶向治疗的未来,以满足不断增长的老年人口的需求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c8a/3941009/ad4fd52f049d/nihms555676f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c8a/3941009/1683ca652dbb/nihms555676f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c8a/3941009/ad4fd52f049d/nihms555676f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c8a/3941009/1683ca652dbb/nihms555676f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c8a/3941009/ad4fd52f049d/nihms555676f2.jpg

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Targeted intraceptor nanoparticle therapy reduces angiogenesis and fibrosis in primate and murine macular degeneration.靶向内受体纳米颗粒疗法可减少灵长类动物和鼠类黄斑变性中的血管生成和纤维化。
ACS Nano. 2013 Apr 23;7(4):3264-75. doi: 10.1021/nn305958y. Epub 2013 Mar 20.
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Inflammatory mediators induced by amyloid-beta in the retina and RPE in vivo: implications for inflammasome activation in age-related macular degeneration.在体视网膜和 RPE 中由淀粉样蛋白-β诱导的炎症介质:对年龄相关性黄斑变性中炎症小体激活的影响。
Invest Ophthalmol Vis Sci. 2013 Mar 1;54(3):2225-37. doi: 10.1167/iovs.12-10849.
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Seven new loci associated with age-related macular degeneration.
美国成年人中有机磷农药暴露与年龄相关性黄斑变性风险之间的关联:来自可解释机器学习方法的分析
Int J Ophthalmol. 2025 Jul 18;18(7):1214-1230. doi: 10.18240/ijo.2025.07.04. eCollection 2025.
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Repurposing Dimethyl Fumarate Targeting Nrf2 to Slow Down the Growth of Areas of Geographic Atrophy.重新利用富马酸二甲酯靶向Nrf2以减缓地图样萎缩区域的生长。
Int J Mol Sci. 2025 Jun 25;26(13):6112. doi: 10.3390/ijms26136112.
5
Factor-H-related protein 1 (FHR1), a promotor of para-inflammation in age-related macular degeneration.补体因子H相关蛋白1(FHR1),年龄相关性黄斑变性中旁炎症的促进因子。
J Neuroinflammation. 2025 Jul 3;22(1):173. doi: 10.1186/s12974-025-03499-z.
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Integrating explainable machine learning and transcriptomics data reveals cell-type specific immune signatures underlying macular degeneration.整合可解释的机器学习和转录组学数据揭示了黄斑变性潜在的细胞类型特异性免疫特征。
NPJ Genom Med. 2025 Jun 14;10(1):48. doi: 10.1038/s41525-025-00507-2.
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