The role of anti-inflammatory agents in age-related macular degeneration (AMD) treatment

被引:123
作者
Wang, Y. [1 ,2 ]
Wang, V. M. [1 ]
Chan, C-C [1 ]
机构
[1] NEI, Immunol Lab, Immunopathol Sect, NIH, Bethesda, MD 20892 USA
[2] Sun Yat Sen Univ, Zhongshan Ophthalm Ctr, Guangzhou 510275, Guangdong, Peoples R China
关键词
age-related macular degeneration; inflammation; corticosteroid; nonsteoridal anti-inflammatory drug; immunosuppressant; biologics; INTRAVITREAL TRIAMCINOLONE ACETONIDE; CHLAMYDIA-PNEUMONIAE INFECTION; PIGMENT EPITHELIAL DETACHMENT; RANDOMIZED CLINICAL-TRIAL; PHOTODYNAMIC THERAPY; CHOROIDAL NEOVASCULARIZATION; TRIPLE THERAPY; COMPLEMENT; BEVACIZUMAB; INJECTION;
D O I
10.1038/eye.2010.196
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Although age-related macular degeneration (AMD) is not a classic inflammatory disease like uveitis, inflammation has been found to have an important role in disease pathogenesis and progression. Innate immunity and autoimmune components, such as complement factors, chemokines, cytokines, macrophages, and ocular microglia, are believed to be heavily involved in AMD development. Targeting these specific inflammatory molecules has recently been explored in an attempt to better understand and treat AMD. Although antivascular endothelial growth factor therapy is the first line of defence against neovascular AMD, anti-inflammatory agents such as corticosteroids, nonsteroidal anti-inflammatory drugs (NSAIDs), immunosuppressive agents (eg, methotrexate and rapamycin), and biologics (eg, infliximab, daclizumab, and complement inhibitors) may provide an adjunct or alternative mechanism to suppress the inflammatory processes driving AMD progression. Further investigation is required to evaluate the long-term safety and efficacy of these drugs for both neovascular and non-neovascular AMD. Eye (2011) 25, 127-139; doi: 10.1038/eye.2010.196; published online 24 December 2010
引用
收藏
页码:127 / 139
页数:13
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