Fixing the leak: targeting the vascular endothelium in sepsis

被引:17
作者
Spicer, Aaron [1 ]
Calfee, Carolyn S. [2 ,3 ]
机构
[1] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Anesthesia, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
关键词
ACUTE LUNG INJURY; EXCESS CIRCULATING ANGIOPOIETIN-2; MULTIPLE-ORGAN DYSFUNCTION; CONTRIBUTE; MORTALITY; COMP-ANG1; SURVIVAL;
D O I
10.1186/cc11829
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Angiopoietin-1 is a Tie-2 receptor agonist that stabilizes vascular endothelium, promoting endothelial maturation and preventing capillary leak. Angiopoietin-2 is largely a competitive partial antagonist that is markedly elevated in humans and animal models of sepsis and other inflammatory states, directly disrupts the endothelial barrier, and has been correlated with end-organ dysfunction and death in sepsis. In the previous issue of Critical Care, Alfieri and colleagues used intravital microscopy to study the microvasculature in a murine model of sepsis. Treatment with a modified angiopoietin-1 molecule led to reversal of albumin vascular leak and improved blood flow to skeletal muscle, as well as a decrease in the levels of several inflammatory cytokines. Importantly, the angiopoietin-1 variant was administered 20 hours after initial lipopolysaccharide challenge. This study adds to the evidence that the angiopoietin/Tie-2 axis represents a modifiable pathway through which targeted therapy may be able to directly reverse part of the pathology of sepsis.
引用
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页数:3
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