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CXCL9 concentrations in cerebrospinal fluid and serum of patients with tick-borne encephalitis

INTRODUCTION: The aim of our current study was to evaluate cerebrospinal fluid (CSF) and serum CXCL9 concentrations and diagnostic usefulness of this molecule in tick-borne encephalitis (TBE). The study included TBE patients in the acute phase (TBE I) and after 2 weeks of follow-up (TBE II). The con...

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Autores principales: Koper, Olga M., Kamińska, Joanna, Grygorczuk, Sambor, Zajkowska, Joanna, Kemona, Halina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868655/
https://www.ncbi.nlm.nih.gov/pubmed/29593804
http://dx.doi.org/10.5114/aoms.2016.58667
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author Koper, Olga M.
Kamińska, Joanna
Grygorczuk, Sambor
Zajkowska, Joanna
Kemona, Halina
author_facet Koper, Olga M.
Kamińska, Joanna
Grygorczuk, Sambor
Zajkowska, Joanna
Kemona, Halina
author_sort Koper, Olga M.
collection PubMed
description INTRODUCTION: The aim of our current study was to evaluate cerebrospinal fluid (CSF) and serum CXCL9 concentrations and diagnostic usefulness of this molecule in tick-borne encephalitis (TBE). The study included TBE patients in the acute phase (TBE I) and after 2 weeks of follow-up (TBE II). The control group consisted of patients investigated for suspected central nervous system (CNS) infection, but with normal CSF findings. MATERIAL AND METHODS: Concentrations of CXCL9 were measured using enzyme-linked immunosorbent assay (ELISA). RESULTS: Cerebrospinal fluid and serum concentrations of CXCL9 in patients with TBE were significantly higher than in controls (p < 0.001). This alteration was also observed in the case of the CXCL9 index (I(CXCL9); CSF CXCL9 concentration divided by serum CXCL9 concentration) (p < 0.001); moreover, I(CXCL9) significantly decreased after 2 weeks (p < 0.001). This is the first study to evaluate the CSF and serum levels of CXCL9 in subjects with TBE. CONCLUSIONS: CXCL9 is a ligand for CXCR3, which was found on all Th1 memory lymphocytes present in the peripheral blood; therefore the elevated concentrations of CXCL9 in TBE patients as compared to the controls might indicate that this chemokine perhaps takes part in the trafficking of Th(1) cells into the CNS. The results presented here support the hypothesis that CXCL9 may play a role in TBE. However, further studies are required to determine whether this protein might be used as a potential tool for the diagnosis and monitoring of inflammation in TBE.
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spelling pubmed-58686552018-03-28 CXCL9 concentrations in cerebrospinal fluid and serum of patients with tick-borne encephalitis Koper, Olga M. Kamińska, Joanna Grygorczuk, Sambor Zajkowska, Joanna Kemona, Halina Arch Med Sci Clinical Research INTRODUCTION: The aim of our current study was to evaluate cerebrospinal fluid (CSF) and serum CXCL9 concentrations and diagnostic usefulness of this molecule in tick-borne encephalitis (TBE). The study included TBE patients in the acute phase (TBE I) and after 2 weeks of follow-up (TBE II). The control group consisted of patients investigated for suspected central nervous system (CNS) infection, but with normal CSF findings. MATERIAL AND METHODS: Concentrations of CXCL9 were measured using enzyme-linked immunosorbent assay (ELISA). RESULTS: Cerebrospinal fluid and serum concentrations of CXCL9 in patients with TBE were significantly higher than in controls (p < 0.001). This alteration was also observed in the case of the CXCL9 index (I(CXCL9); CSF CXCL9 concentration divided by serum CXCL9 concentration) (p < 0.001); moreover, I(CXCL9) significantly decreased after 2 weeks (p < 0.001). This is the first study to evaluate the CSF and serum levels of CXCL9 in subjects with TBE. CONCLUSIONS: CXCL9 is a ligand for CXCR3, which was found on all Th1 memory lymphocytes present in the peripheral blood; therefore the elevated concentrations of CXCL9 in TBE patients as compared to the controls might indicate that this chemokine perhaps takes part in the trafficking of Th(1) cells into the CNS. The results presented here support the hypothesis that CXCL9 may play a role in TBE. However, further studies are required to determine whether this protein might be used as a potential tool for the diagnosis and monitoring of inflammation in TBE. Termedia Publishing House 2016-03-22 2018-03 /pmc/articles/PMC5868655/ /pubmed/29593804 http://dx.doi.org/10.5114/aoms.2016.58667 Text en Copyright: © 2016 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Clinical Research
Koper, Olga M.
Kamińska, Joanna
Grygorczuk, Sambor
Zajkowska, Joanna
Kemona, Halina
CXCL9 concentrations in cerebrospinal fluid and serum of patients with tick-borne encephalitis
title CXCL9 concentrations in cerebrospinal fluid and serum of patients with tick-borne encephalitis
title_full CXCL9 concentrations in cerebrospinal fluid and serum of patients with tick-borne encephalitis
title_fullStr CXCL9 concentrations in cerebrospinal fluid and serum of patients with tick-borne encephalitis
title_full_unstemmed CXCL9 concentrations in cerebrospinal fluid and serum of patients with tick-borne encephalitis
title_short CXCL9 concentrations in cerebrospinal fluid and serum of patients with tick-borne encephalitis
title_sort cxcl9 concentrations in cerebrospinal fluid and serum of patients with tick-borne encephalitis
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5868655/
https://www.ncbi.nlm.nih.gov/pubmed/29593804
http://dx.doi.org/10.5114/aoms.2016.58667
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