Department of Ophthalmology, University of Bonn, Bonn, Germany; Department of Ophthalmology, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
Institute of Molecular Medicine and Experimental Immunology, University of Bonn, Bonn, Germany; Asia-Pacific Centre for Animal Health, Faculty of Science, University of Melbourne, Melbourne, Australia.
Surv Ophthalmol. 2024 Nov-Dec;69(6):851-869. doi: 10.1016/j.survophthal.2024.07.009. Epub 2024 Aug 6.
We provide an overview of the expanding literature on the role of cytokines and immune mediators in pathophysiology of age-related macular degeneration (AMD). Although many immunological mediators have been linked to AMD pathophysiology, the broader mechanistic picture remains unclear with substantial variations in the levels of evidence supporting these mediators. Therefore, we reviewed the literature considering the varying levels of supporting evidence. A Medical Subject Headings (MeSH) term-based literature research was conducted in September, 2023, consisting of the MeSH terms "cytokine" and "Age-related macular degeneration" connected by the operator "AND". After screening the publications by title, abstract, and full text, a total of 146 publications were included. The proinflammatory cytokines IL-1β (especially in basic research studies), IL-6, IL-8, IL-18, TNF-α, and MCP-1 are the most extensively characterised cytokines/chemokines, highlighting the role of local inflammasome activation and altered macrophage function in the AMD pathophysiology. Among the antiinflammatory mediators IL-4, IL-10, and TGF-β were found to be the most extensively characterised, with IL-4 driving and IL-10 and TGF-β suppressing disease progression. Despite the extensive literature on this topic, a profound understanding of AMD pathophysiology has not yet been achieved. Therefore, further studies are needed to identify potential therapeutic targets, followed by clinical studies.
我们提供了一个关于细胞因子和免疫介质在年龄相关性黄斑变性(AMD)病理生理学中作用的不断扩大的文献综述。尽管许多免疫介质与 AMD 病理生理学有关,但更广泛的机制图景仍然不清楚,这些介质的证据水平存在很大差异。因此,我们考虑到证据支持的不同水平,对文献进行了综述。我们于 2023 年 9 月进行了基于医学主题词(MeSH)术语的文献研究,其中包括 MeSH 术语“细胞因子”和“年龄相关性黄斑变性”,并用运算符“AND”连接。在通过标题、摘要和全文筛选出版物后,共纳入了 146 篇出版物。促炎细胞因子 IL-1β(特别是在基础研究中)、IL-6、IL-8、IL-18、TNF-α 和 MCP-1 是研究最广泛的细胞因子/趋化因子,突出了局部炎症小体激活和巨噬细胞功能改变在 AMD 病理生理学中的作用。在抗炎介质中,IL-4、IL-10 和 TGF-β 的研究最为广泛,其中 IL-4 驱动疾病进展,而 IL-10 和 TGF-β 抑制疾病进展。尽管关于这个主题的文献很多,但对 AMD 病理生理学还没有深入的了解。因此,需要进一步的研究来确定潜在的治疗靶点,然后进行临床研究。