[1]王春明,冯宇梁,李佳,等. 年龄相关性黄斑变性治疗药物研究进展及未来研发方向[J].眼科新进展,2015,35(6):597-600.[doi:10.13389/j.cnki.rao.2015.0162]
 WANG Chun-Ming,FENG Yu-Liang,LI Jia,et al. Progress in drug treatment development for age-related macular degeneration[J].Recent Advances in Ophthalmology,2015,35(6):597-600.[doi:10.13389/j.cnki.rao.2015.0162]
点击复制

 年龄相关性黄斑变性治疗药物研究进展及未来研发方向
分享到:

《眼科新进展》[ISSN:1003-5141/CN:41-1105/R]

卷:
35卷
期数:
2015年6期
页码:
597-600
栏目:
文献综述
出版日期:
2015-06-05

文章信息/Info

Title:
 Progress in drug treatment development for age-related macular degeneration
作者:
 王春明冯宇梁李佳张明俞德超
 215123 江苏省苏州市,信达生物制药(苏州)有限公司
Author(s):
 WANG Chun-Ming FENG Yu-Liang LI JiaZHANG Ming YU De-Chao
 Innovent Biologics, Inc. Suzhou 215 1 23 , Jiangsu Province, China
关键词:
 年龄相关性黄斑变性血管内皮生长因子纤维化瘢痕地图样萎缩补体血小板衍生生长因子
Keywords:
 age-related macular degenerationvascular endothelial growth factor fibrosis scarrrng geographic atrophy complement platelet- derived growth factor
DOI:
10.13389/j.cnki.rao.2015.0162
文献标志码:
A
摘要:
 年龄相关性黄斑变性是导致老年人失明的主要病因。虽然目前以雷珠单抗为代表的抗血管内皮生长因子(vascularendothelialgrowthfactor,VEGF)药物已经成为年龄相关性黄斑变性的标准治疗药物,但是长期抗VEGF治疗后不仅疗效下降,同时会诱导视网膜纤维化、瘢痕和地图样萎缩等多种并发症,所以开发新的治疗药物单用或者与抗VEGF药物联合应用或者开发多靶点治疗药物成为新的研究方向。目前已经有一些以补体和血小板衍生生长因子为靶点的治疗药物在早期的临床研究中表现出了令人鼓舞的疗效。我们就目前年龄相关性黄斑变性治疗药物研究进展及未来研究方向作一综述。
Abstract:
 Age-related macular degeneration ( AMD) is a major contributor to blindness in the elderly. Recently, anti-vascular endothelial growth factor antibody drugs , represented by Ranibizumab , have become a standard therapy against AMD ; However . after long-term treatment not only therapeutic effects decline , but retinal fibrosis . scarring and geographic atrophy are induced. Thus , the exploration of new drugs used as a mono-therapy or in combination with anti- vascular endothelial growth factor antibody drugs or multi-target drugs is the most hopeful research and development direction in the future. Recently, complement and platelet-derived growth factor-targeting drugs have demonstrated encouraging results during early clinical trials.

相似文献/References:

[1]范姜砾 王雨生 张鹏.湿性年龄相关性黄斑变性患者血浆中相关抗氧化酶水平测定[J].眼科新进展,2012,32(5):000.
[2]王毅 李罗翔 李娟 曾庆华.ApoE基因缺失小鼠视网膜及Bruch膜组织形态观察[J].眼科新进展,2013,33(1):000.
[3]徐新荣 仲路 黄冰林 魏源华 周欣 王玲 王富强.年龄相关性黄斑变性血浆蛋白质组学初步研究[J].眼科新进展,2013,33(2):000.
[4]党亚龙 陈彬川 穆雅林 赵满丽 朱豫.i-MP对产生2型脉络膜新生血管的年龄相关性黄斑变性患者视力及黄斑厚度的影响[J].眼科新进展,2013,33(2):000.
[5]王毅 李罗翔 李进辉 李娟 曾庆华.血脂异常ApoE基因缺失小鼠视网膜色素上皮细胞胞浆内黑色素和脂褐素的改变[J].眼科新进展,2013,33(7):000.
[6]罗文婷 孙大卫.血管黏附蛋白-1在眼科疾病中的研究进展[J].眼科新进展,2013,33(8):000.
[7]陆秉文 吴星伟.光动力疗法治疗年龄相关性黄斑变性的研究进展[J].眼科新进展,2013,33(4):000.
[8]栾兰 姚勇.湿性年龄相关性黄斑变性的治疗进展[J].眼科新进展,2013,33(4):000.
[9]胡艳红 祁明信 郭娜 陈胜 柯发杰.渗出型年龄相关性黄斑变性患者外周血CCR3的表达[J].眼科新进展,2013,33(11):000.
[10]刘平 苏胜. 白内障蛋白质组学研究的现状及未来研究方向[J].眼科新进展,2014,34(1):001.
[11]魏菁,黄厚斌. 吲哚青绿介导的光栓塞治疗黄斑中心凹下脉络膜新生血管[J].眼科新进展,2014,34(9):842.[doi:10.13389/j.cnki.rao.2014.0232]
[12]俞永珍,邹秀兰,邹玉平. 氧化应激及抗氧化物在年龄相关性黄斑变性中的作用[J].眼科新进展,2015,35(5):489.[doi:10.13389/j.cnki.rao.2015.0134]
 YU Yong-Zhen,ZOU Xiu-Lan,ZOU Yu-Ping. Roles of oxidative stress and antioxidants in age related macular degeneration[J].Recent Advances in Ophthalmology,2015,35(6):489.[doi:10.13389/j.cnki.rao.2015.0134]
[13]张跃红,饶志波,刘娟,等. 低浓度β-淀粉样蛋白抑制小鼠视网膜色素上皮细胞P-糖蛋白的功能性表达[J].眼科新进展,2015,35(9):801.[doi:10.13389/j.cnki.rao.2015.0220]
 ZHANG Yue-Hong,RAO Zhi-Bo,LIU Juan,et al. Low concentration of amyloid β-protein inhibiting functional expression of P-glycoprotein in mouse retinal pigment epithelial cells[J].Recent Advances in Ophthalmology,2015,35(6):801.[doi:10.13389/j.cnki.rao.2015.0220]

更新日期/Last Update: 2015-06-01