Radioimmunoassay versus flow cytometric assay to quantify LPS-binding protein (LBP) concentrations in human plasma.

Détails

ID Serval
serval:BIB_99DB066FC3CA
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Radioimmunoassay versus flow cytometric assay to quantify LPS-binding protein (LBP) concentrations in human plasma.
Périodique
Journal of immunological methods
Auteur⸱e⸱s
Heumann D., Gallay P., Le Roy D., Landmann R., Glauser M.P.
ISSN
0022-1759 (Print)
ISSN-L
0022-1759
Statut éditorial
Publié
Date de publication
16/05/1994
Peer-reviewed
Oui
Volume
171
Numéro
2
Pages
169-176
Langue
anglais
Notes
Publication types: Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
LPS-binding protein (LBP) is an acute phase protein present in plasma, that has been shown to play a major role in sensitizing monocytes to LPS. We describe here two assays to quantify LBP in plasma. The first assay made use of monophosphoryl lipid A to capture LBP in human plasma, and LBP was detected by radiolabeled anti-LBP IgG. The second assay measured LBP by flow cytometry, using LBPs ability to present LPS to the CD14 receptor present on monocytes. Both assays had a similar level of sensitivity, that allowed the quantification of LBP in human plasma.
Mots-clé
Acute-Phase Proteins/analysis, Antibody Specificity, Carrier Proteins/blood, Flow Cytometry, Humans, Immunoglobulin G, Lipid A/analogs & derivatives, Membrane Glycoproteins, Radioimmunoassay, Sensitivity and Specificity
Pubmed
Web of science
Création de la notice
06/08/2018 11:33
Dernière modification de la notice
20/08/2019 16:01
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