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Elevated production of radical oxygen species by polymorphonuclear neutrophils in cerebrospinal fluid infection

BACKGROUND: Central nervous system infection is a daily concern in neurointensive care; however, diagnosis remains difficult because classical criteria based on cerebrospinal fluid (CSF) analysis are difficult to interpret in post-trauma or neurosurgery patients after recent bleeding. A rapid, speci...

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Autores principales: Lukaszewicz, Anne-Claire, Gontier, Géraldine, Faivre, Valérie, Ouanounou, Ingrid, Payen, Didier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359206/
https://www.ncbi.nlm.nih.gov/pubmed/22490368
http://dx.doi.org/10.1186/2110-5820-2-10
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author Lukaszewicz, Anne-Claire
Gontier, Géraldine
Faivre, Valérie
Ouanounou, Ingrid
Payen, Didier
author_facet Lukaszewicz, Anne-Claire
Gontier, Géraldine
Faivre, Valérie
Ouanounou, Ingrid
Payen, Didier
author_sort Lukaszewicz, Anne-Claire
collection PubMed
description BACKGROUND: Central nervous system infection is a daily concern in neurointensive care; however, diagnosis remains difficult because classical criteria based on cerebrospinal fluid (CSF) analysis are difficult to interpret in post-trauma or neurosurgery patients after recent bleeding. A rapid, specific, sensitive test to diagnose CSF infection would help streamline therapeutic decisions in clinical practice and limit the risk of multiresistant bacteria. We hypothesized that polymorphonuclear neutrophil (PMN) phenotype and radical oxygen species (ROS) production in CSF may be specific to the presence of infection. METHODS: This study included 30 patients with suspected CSF infection with ventricular hemorrhage requiring external ventricular drainage, and 13 patients after trauma or surgery. Criteria for evaluating CSF infection included positive culture and > 100 leukocytes/mm(3). Analysis of PMN phenotype was performed using flow cytometry (CD16, CD11b, and CD62L). ROS production was analyzed through luminometry (luminol). RESULTS: Infected CSF exhibited higher production of ROS compared with noninfected CSF. PMNs in CSF exhibited low CD16 and high annexin V expression, suggesting apoptosis. CONCLUSIONS: Measurement of ROS production may discriminate infected from noninfected CSF. This simple test would be easy to employ in clinical practice to improve CSF infection management.
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spelling pubmed-33592062012-06-05 Elevated production of radical oxygen species by polymorphonuclear neutrophils in cerebrospinal fluid infection Lukaszewicz, Anne-Claire Gontier, Géraldine Faivre, Valérie Ouanounou, Ingrid Payen, Didier Ann Intensive Care Research BACKGROUND: Central nervous system infection is a daily concern in neurointensive care; however, diagnosis remains difficult because classical criteria based on cerebrospinal fluid (CSF) analysis are difficult to interpret in post-trauma or neurosurgery patients after recent bleeding. A rapid, specific, sensitive test to diagnose CSF infection would help streamline therapeutic decisions in clinical practice and limit the risk of multiresistant bacteria. We hypothesized that polymorphonuclear neutrophil (PMN) phenotype and radical oxygen species (ROS) production in CSF may be specific to the presence of infection. METHODS: This study included 30 patients with suspected CSF infection with ventricular hemorrhage requiring external ventricular drainage, and 13 patients after trauma or surgery. Criteria for evaluating CSF infection included positive culture and > 100 leukocytes/mm(3). Analysis of PMN phenotype was performed using flow cytometry (CD16, CD11b, and CD62L). ROS production was analyzed through luminometry (luminol). RESULTS: Infected CSF exhibited higher production of ROS compared with noninfected CSF. PMNs in CSF exhibited low CD16 and high annexin V expression, suggesting apoptosis. CONCLUSIONS: Measurement of ROS production may discriminate infected from noninfected CSF. This simple test would be easy to employ in clinical practice to improve CSF infection management. Springer 2012-04-10 /pmc/articles/PMC3359206/ /pubmed/22490368 http://dx.doi.org/10.1186/2110-5820-2-10 Text en Copyright ©2012 Lukaszewicz et al; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Lukaszewicz, Anne-Claire
Gontier, Géraldine
Faivre, Valérie
Ouanounou, Ingrid
Payen, Didier
Elevated production of radical oxygen species by polymorphonuclear neutrophils in cerebrospinal fluid infection
title Elevated production of radical oxygen species by polymorphonuclear neutrophils in cerebrospinal fluid infection
title_full Elevated production of radical oxygen species by polymorphonuclear neutrophils in cerebrospinal fluid infection
title_fullStr Elevated production of radical oxygen species by polymorphonuclear neutrophils in cerebrospinal fluid infection
title_full_unstemmed Elevated production of radical oxygen species by polymorphonuclear neutrophils in cerebrospinal fluid infection
title_short Elevated production of radical oxygen species by polymorphonuclear neutrophils in cerebrospinal fluid infection
title_sort elevated production of radical oxygen species by polymorphonuclear neutrophils in cerebrospinal fluid infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359206/
https://www.ncbi.nlm.nih.gov/pubmed/22490368
http://dx.doi.org/10.1186/2110-5820-2-10
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