Title of article :
The etiology of sepsis: turned inside out
Author/Authors :
Gregory J. Brunn، نويسنده , , Jeffrey L. Platt، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2006
Pages :
7
From page :
10
To page :
16
Abstract :
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.
Journal title :
Trends in Molecular Medicine
Serial Year :
2006
Journal title :
Trends in Molecular Medicine
Record number :
784376
Link To Document :
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