Targeting leukocyte integrins in human diseases

被引:122
|
作者
Yonekawa, K
Harlan, JM
机构
[1] Univ Washington, Div Nephrol, Dept Pediat, Seattle, WA 98195 USA
[2] Univ Washington, Div Hematol, Dept Med, Seattle, WA 98195 USA
关键词
adhesion; clinical; trials; inflammation;
D O I
10.1189/jlb.0804460
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
As our understanding of integrins as multifunctional adhesion and signaling molecules has grown, so has their recognition as potential therapeutic targets in human diseases. Leukocyte integrins are of particular interest in this regard, as they are key molecules in immune-mediated and inflammatory processes and are thus critically involved in diverse clinical disorders, ranging from asthma to atherosclerosis. Antagonists that interfere with integrin-dependent leukocyte trafficking and/or post-trafficking events have shown efficacy in multiple preclinical models, but these have not always predicted success in subsequent clinical trials (e.g., ischemia-reperfusion disorders and transplantation). However, recent successes of integrin antagonists in psoriasis, inflammatory bowel disease, and multiple sclerosis demonstrate the tremendous potential of anti-adhesion therapy directed at leukocyte integrins. This article will review the role of the leukocyte integrins in the inflammatory process, approaches to targeting leukocyte integrins and their ligands, and the results of completed clinical trials.
引用
收藏
页码:129 / 140
页数:12
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