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Proinflammatory Cytokines in Antilipopolysaccharide Immunity Against Klebsiella Infections

This study was undertaken in order to determine whether proinflammatory cytokines are involved in a previously described protection against Klebsiella infection mediated by antilipopolysaccharide antibodies. BALB/c mice were infected intraperitoneally with a lethal challenge of Klebsiella pneumoniae...

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Detalles Bibliográficos
Autores principales: Rukavina, Tomislav, Vasiljev, Vanja, Ticac, Brigita
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1533908/
https://www.ncbi.nlm.nih.gov/pubmed/16030391
http://dx.doi.org/10.1155/MI.2005.88
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author Rukavina, Tomislav
Vasiljev, Vanja
Ticac, Brigita
author_facet Rukavina, Tomislav
Vasiljev, Vanja
Ticac, Brigita
author_sort Rukavina, Tomislav
collection PubMed
description This study was undertaken in order to determine whether proinflammatory cytokines are involved in a previously described protection against Klebsiella infection mediated by antilipopolysaccharide antibodies. BALB/c mice were infected intraperitoneally with a lethal challenge of Klebsiella pneumoniae Caroli. One group of mice was protected with monoclonal antibodies against lipopolysaccharide prior to infection and the second was not. We determined the number of colony-forming units at different time points in the blood of infected animals and paralleled them with plasma levels of five proinflammatory cytokines measured by enzyme immunoassays. Our results show that the two groups of animals tested expressed different plasma concentrations for all cytokines. The greatest difference was detected 24 hours after infection, with a higher production in the unprotected group. We concluded that a reduced cytokine production is partially responsible for the survival of protected animals.
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spelling pubmed-15339082006-08-21 Proinflammatory Cytokines in Antilipopolysaccharide Immunity Against Klebsiella Infections Rukavina, Tomislav Vasiljev, Vanja Ticac, Brigita Mediators Inflamm Research Communication This study was undertaken in order to determine whether proinflammatory cytokines are involved in a previously described protection against Klebsiella infection mediated by antilipopolysaccharide antibodies. BALB/c mice were infected intraperitoneally with a lethal challenge of Klebsiella pneumoniae Caroli. One group of mice was protected with monoclonal antibodies against lipopolysaccharide prior to infection and the second was not. We determined the number of colony-forming units at different time points in the blood of infected animals and paralleled them with plasma levels of five proinflammatory cytokines measured by enzyme immunoassays. Our results show that the two groups of animals tested expressed different plasma concentrations for all cytokines. The greatest difference was detected 24 hours after infection, with a higher production in the unprotected group. We concluded that a reduced cytokine production is partially responsible for the survival of protected animals. Hindawi Publishing Corporation 2005-06-09 /pmc/articles/PMC1533908/ /pubmed/16030391 http://dx.doi.org/10.1155/MI.2005.88 Text en Hindawi Publishing Corporation
spellingShingle Research Communication
Rukavina, Tomislav
Vasiljev, Vanja
Ticac, Brigita
Proinflammatory Cytokines in Antilipopolysaccharide Immunity Against Klebsiella Infections
title Proinflammatory Cytokines in Antilipopolysaccharide Immunity Against Klebsiella Infections
title_full Proinflammatory Cytokines in Antilipopolysaccharide Immunity Against Klebsiella Infections
title_fullStr Proinflammatory Cytokines in Antilipopolysaccharide Immunity Against Klebsiella Infections
title_full_unstemmed Proinflammatory Cytokines in Antilipopolysaccharide Immunity Against Klebsiella Infections
title_short Proinflammatory Cytokines in Antilipopolysaccharide Immunity Against Klebsiella Infections
title_sort proinflammatory cytokines in antilipopolysaccharide immunity against klebsiella infections
topic Research Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1533908/
https://www.ncbi.nlm.nih.gov/pubmed/16030391
http://dx.doi.org/10.1155/MI.2005.88
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