Suppr超能文献

年龄相关性黄斑变性中巨噬细胞和白细胞介素-17 的分子病理学。

Molecular pathology of macrophages and interleukin-17 in age-related macular degeneration.

机构信息

Section of Immunopathology, Laboratory of Immunology, National Eye Institute, National Institutes of Health, 10 Center Drive, 10/10N103, 20892-1857, Bethesda, MD, USA,

出版信息

Adv Exp Med Biol. 2014;801:193-8. doi: 10.1007/978-1-4614-3209-8_25.

Abstract

The pathology of age-related macular degeneration (AMD) is characterized by degeneration of photoreceptors and retinal pigment epithelial cells as well as by changes of choroidal capillaries in the macula. Although AMD is not a typical uveitis, there is a consistence and an imbalance of ocular para-inflammation. Ocular inflammation, particularly in the macula, plays a critical role in AMD pathogenesis. The inflammatory and immune-related elements involved in AMD include inflammatory and related cells as well as the secreted molecules and factors from these cells. Innate immune system elements such as macrophages and cytokines play an important role in AMD pathology and pathogenesis. This chapter reviews the observed deviation in macrophage plasticity and the elevated expression of interleukin-17 in AMD eyes while discussing potential contributions to AMD pathogenesis. Targeting of these specific inflammatory pathways and molecules at appropriate times should be explored and may become promising novel adjunct agents to AMD therapy.

摘要

年龄相关性黄斑变性(AMD)的病理学特征为光感受器和视网膜色素上皮细胞的变性,以及黄斑部脉络膜毛细血管的改变。虽然 AMD 不是典型的葡萄膜炎,但存在一致性和眼旁炎症的失衡。眼部炎症,特别是在黄斑部,在 AMD 的发病机制中起着关键作用。涉及 AMD 的炎症和免疫相关因素包括炎症和相关细胞以及这些细胞分泌的分子和因子。先天免疫系统元素,如巨噬细胞和细胞因子,在 AMD 的病理学和发病机制中起着重要作用。本章通过讨论 AMD 发病机制中可能的贡献,综述了观察到的巨噬细胞可塑性偏差和白细胞介素-17 在 AMD 眼中的高表达。在适当的时候针对这些特定的炎症途径和分子进行靶向治疗,可能成为 AMD 治疗的有前途的新型辅助药物。

相似文献

2
Inflammatory biomarkers for AMD.AMD 的炎症生物标志物。
Adv Exp Med Biol. 2014;801:251-7. doi: 10.1007/978-1-4614-3209-8_32.
3
Macrophages and Age-Related Macular Degeneration.巨噬细胞与年龄相关性黄斑变性
Adv Exp Med Biol. 2025;1468:9-13. doi: 10.1007/978-3-031-76550-6_2.
10
Inflammation in age-related macular degeneration.年龄相关性黄斑变性中的炎症。
Adv Exp Med Biol. 2014;801:229-35. doi: 10.1007/978-1-4614-3209-8_30.

引用本文的文献

6
Contribution of Interleukin-17A to Retinal Degenerative Diseases.白细胞介素-17A 对视网膜退行性疾病的贡献。
Front Immunol. 2022 Mar 22;13:847937. doi: 10.3389/fimmu.2022.847937. eCollection 2022.
9
The Role of Inflammation in Age-Related Macular Degeneration.炎症在年龄相关性黄斑变性中的作用。
Int J Biol Sci. 2020 Sep 23;16(15):2989-3001. doi: 10.7150/ijbs.49890. eCollection 2020.

本文引用的文献

9
Advanced age impairs macrophage polarization.高龄会损害巨噬细胞的极化。
J Interferon Cytokine Res. 2012 Jan;32(1):18-26. doi: 10.1089/jir.2011.0058. Epub 2011 Dec 16.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验