Anti-Inflammatory Therapy in Chronic Disease: Challenges and Opportunities

被引:947
作者
Tabas, Ira [1 ,2 ]
Glass, Christopher K. [3 ,4 ]
机构
[1] Columbia Univ, Dept Med, Dept Anat & Cell Biol, New York, NY 10032 USA
[2] Columbia Univ, Dept Physiol & Cellular Biophys, New York, NY 10032 USA
[3] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
REGULATORY T-CELLS; INSULIN-RESISTANCE; PPAR-GAMMA; INFLAMMATORY RESPONSE; ADENOSINE A(2A); GENE-EXPRESSION; RESOLVIN D2; ATHEROSCLEROSIS; INHIBITION; METHOTREXATE;
D O I
10.1126/science.1230720
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
A number of widespread and devastating chronic diseases, including atherosclerosis, type 2 diabetes, and Alzheimer's disease, have a pathophysiologically important inflammatory component. In these diseases, the precise identity of the inflammatory stimulus is often unknown and, if known, is difficult to remove. Thus, there is interest in therapeutically targeting the inflammatory response. Although there has been success with anti-inflammatory therapy in chronic diseases triggered by primary inflammation dysregulation or autoimmunity, there are considerable limitations. In particular, the inflammatory response is critical for survival. As a result, redundancy, compensatory pathways, and necessity narrow the risk: benefit ratio of anti-inflammatory drugs. However, new advances in understanding inflammatory signaling and its links to resolution pathways, together with new drug development, offer promise in this area of translational biomedical research.
引用
收藏
页码:166 / 172
页数:7
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