Abstract
Because lipopolysaccharide (LPS)-binding protein (LBP) sensitizes monocytes to LPS in vitro, it has been suggested that LBP initiates host defenses against Gram-negative bacteria. The role of LBP in vivo, and particularly in endotoxemic shock, is unknown, however. Therefore an IgG against murine LBP was prepared. It was found to neutralize binding of LPS and subsequent activation of murine macrophages in vitro. This anti-LBP protected mice against the lethal effect of LPS when given at the same time as LPS challenge, but it failed to protect mice when delayed 15 min after LPS challenge. The same preparation was also effective after challenge with lipid A but not after challenge with Staphylococcus aureus enterotoxin. The protection was correlated with a strong decrease of circulating tumor necrosis factor. These data demonstrate that in vivo LBP is a major mediator of the lethal effects of endotoxemia.
MeSH Terms
Acute-Phase Proteins/metabolism
Animals
Bone Marrow
Carrier Proteins/blood,isolation & purification
Chromatography, Ion Exchange
Electrophoresis, Polyacrylamide Gel
Escherichia coli
Hematopoietic Stem Cells
Immunoblotting
Immunoglobulin G/pharmacology
Kinetics
Lipopolysaccharides/metabolism
Macrophages/metabolism
Membrane Glycoproteins
Mice
Mice, Inbred Strains
Shock, Septic/blood
Time Factors
Tumor Necrosis Factor-alpha/metabolism
Chemicals
Acute-Phase Proteins
Carrier Proteins
Immunoglobulin G
Lipopolysaccharides
Membrane Glycoproteins
Tumor Necrosis Factor-alpha
lipopolysaccharide-binding protein
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Gallay P
Department of Internal Medicine, CHUV-1011 Lausanne, Switzerland.
Heumann D
Le Roy D
Barras C
Glauser M P
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