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Toll-like receptor-4 antagonist eritoran tetrasodium for severe sepsis.
- Source :
-
Expert review of anti-infective therapy [Expert Rev Anti Infect Ther] 2011 May; Vol. 9 (5), pp. 507-20. - Publication Year :
- 2011
-
Abstract
- The human innate immune system initiates inflammation in response to bacterial molecules, particularly Gram-negative bacterial endotoxin. The steps by which endotoxin exposure leads to systemic inflammation include binding to Toll-like receptor-4 that specifically recognizes endotoxin and subsequently triggers cellular and molecular inflammatory responses. Severe sepsis is a systemic inflammatory response to infection that induces organ dysfunction and threatens a person's survival. Severe sepsis is frequently associated with increased blood levels of endotoxin. It is a significant medical problem that effects approximately 700,000 patients every year in the USA, resulting in 250,000 deaths. Eritoran tetrasodium is a nonpathogenic analog of bacterial endotoxin that antagonizes inflammatory signaling by the immune receptor Toll-like receptor-4. Eritoran is being evaluated for the treatment of patients with severe sepsis.
- Subjects :
- Antibodies, Neutralizing immunology
Antibodies, Neutralizing therapeutic use
Clinical Trials as Topic
Female
Gram-Negative Bacteria growth & development
Gram-Positive Bacteria growth & development
Humans
Lipopolysaccharides metabolism
Male
Phospholipids metabolism
Renal Dialysis
Sepsis microbiology
Sepsis physiopathology
Signal Transduction drug effects
Toll-Like Receptor 4 immunology
United States
Disaccharides administration & dosage
Disaccharides pharmacokinetics
Lipopolysaccharides adverse effects
Sepsis drug therapy
Sepsis immunology
Sugar Phosphates administration & dosage
Sugar Phosphates pharmacokinetics
Toll-Like Receptor 4 antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1744-8336
- Volume :
- 9
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Expert review of anti-infective therapy
- Publication Type :
- Academic Journal
- Accession number :
- 21609262
- Full Text :
- https://doi.org/10.1586/eri.11.27