The etiology of sepsis: turned inside out

被引:29
作者
Brunn, GJ
Platt, JL [1 ]
机构
[1] Mayo Clin, Coll Med, Dept Pharmacol & Expt Therapeut, Rochester, MN 55905 USA
[2] Mayo Clin, Coll Med, Dept Immunol, Rochester, MN 55905 USA
[3] Mayo Clin, Coll Med, Dept Surg, Rochester, MN 55905 USA
[4] Mayo Clin, Coll Med, Dept Pediat, Rochester, MN 55905 USA
关键词
D O I
10.1016/j.molmed.2005.11.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The sepsis syndrome is thought to occur when microbial products activate Toll-like receptors stimulating widespread inflammation, in turn causing organ failure, shock and death. However, recent discoveries reveal that: (i) not only microbial substances but also endogenous molecules can trigger Toll-like receptors; (ii) Toll-like receptor-4, the endotoxin receptor, is constitutively suppressed; and (iii) the first step in sepsis could be the release of Toll-like receptor-4 from suppression. These discoveries suggest that endotoxin might not always initiate the sepsis syndrome and they explain why anti-endotoxin therapies fail. The discoveries also suggest new therapeutic targets - endogenous agonists and Toll-like receptor regulators - for treatment of sepsis.
引用
收藏
页码:10 / 16
页数:7
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