Restoring HOmeostasis: is heme oxygenase-1 ready for the clinic?

被引:38
作者
Scott, Jeffrey R. [1 ]
Chin, Beek Y. [1 ]
Bilban, Martin H. [1 ]
Otterbein, Leo E. [1 ]
机构
[1] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Transplant Res Ctr,Dept Surg, Boston, MA 02215 USA
关键词
D O I
10.1016/j.tips.2007.03.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Inflammation and immunity result in a wide range of disease processes, including atherosclerosis, vascular thrombosis and sepsis. Heme oxygenase-1 (HO-1) is a key enzyme that is integral to the temporal and spatial regulation of the host response and, together with its products carbon monoxide (CO) and bilirubin, is crucial for maintaining homeostasis and the preservation of function and life. An increasing number of reports demonstrates that HO-1, CO and billirubin regulate the immune response. As CO and bilirubin enter clinical trials, there are obstacles to be addressed before their full therapeutic potential can be achieved. In this article, we delineate the challenges that lie ahead regarding toxicity, pharmacokinetics and mechanisms of action to be able to take full advantage of the powerful cytoprotective properties of these agents for clinical benefit.
引用
收藏
页码:200 / 205
页数:6
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