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Tumour Necrosis Factor-α Production and Immune Cell Activation in Tuberculous Meningitis

The local production of tumour necrosis factor-α (TNFα) was evaluated in the cerebrospinal fluid (CSF) from ten patients with tuberculous meningitis (TBM). The degree of intrathecal immune activation was also studied by assessing the CSF levels of β(2)-microglobulin (β(2)-M) and adenosine deaminase...

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Autores principales: Mastroianni, C. M., Paoletti, F., Valenti, C., Massetti, A. P., Vullo, V., Delia, S.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 1994
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2367021/
https://www.ncbi.nlm.nih.gov/pubmed/18472925
http://dx.doi.org/10.1155/S0962935194000104
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author Mastroianni, C. M.
Paoletti, F.
Valenti, C.
Massetti, A. P.
Vullo, V.
Delia, S.
author_facet Mastroianni, C. M.
Paoletti, F.
Valenti, C.
Massetti, A. P.
Vullo, V.
Delia, S.
author_sort Mastroianni, C. M.
collection PubMed
description The local production of tumour necrosis factor-α (TNFα) was evaluated in the cerebrospinal fluid (CSF) from ten patients with tuberculous meningitis (TBM). The degree of intrathecal immune activation was also studied by assessing the CSF levels of β(2)-microglobulin (β(2)-M) and adenosine deaminase activity (ADA). Results indicate that elevated CSF concentrations of TNFα, β(2)-M and ADA were found in all TBM patients. Moreover, TNFα is produced and selectively concentrated for a long period of time, while β(2)-M and ADA values progressively decline during the course of TBM. Our findings suggest that in TBM patients, after an early activation of immune cells, there is an enhanced and continuous production of TNFα at the site of infection.
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spelling pubmed-23670212008-05-12 Tumour Necrosis Factor-α Production and Immune Cell Activation in Tuberculous Meningitis Mastroianni, C. M. Paoletti, F. Valenti, C. Massetti, A. P. Vullo, V. Delia, S. Mediators Inflamm Research Article The local production of tumour necrosis factor-α (TNFα) was evaluated in the cerebrospinal fluid (CSF) from ten patients with tuberculous meningitis (TBM). The degree of intrathecal immune activation was also studied by assessing the CSF levels of β(2)-microglobulin (β(2)-M) and adenosine deaminase activity (ADA). Results indicate that elevated CSF concentrations of TNFα, β(2)-M and ADA were found in all TBM patients. Moreover, TNFα is produced and selectively concentrated for a long period of time, while β(2)-M and ADA values progressively decline during the course of TBM. Our findings suggest that in TBM patients, after an early activation of immune cells, there is an enhanced and continuous production of TNFα at the site of infection. Hindawi Publishing Corporation 1994 /pmc/articles/PMC2367021/ /pubmed/18472925 http://dx.doi.org/10.1155/S0962935194000104 Text en Copyright © 1994 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mastroianni, C. M.
Paoletti, F.
Valenti, C.
Massetti, A. P.
Vullo, V.
Delia, S.
Tumour Necrosis Factor-α Production and Immune Cell Activation in Tuberculous Meningitis
title Tumour Necrosis Factor-α Production and Immune Cell Activation in Tuberculous Meningitis
title_full Tumour Necrosis Factor-α Production and Immune Cell Activation in Tuberculous Meningitis
title_fullStr Tumour Necrosis Factor-α Production and Immune Cell Activation in Tuberculous Meningitis
title_full_unstemmed Tumour Necrosis Factor-α Production and Immune Cell Activation in Tuberculous Meningitis
title_short Tumour Necrosis Factor-α Production and Immune Cell Activation in Tuberculous Meningitis
title_sort tumour necrosis factor-α production and immune cell activation in tuberculous meningitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2367021/
https://www.ncbi.nlm.nih.gov/pubmed/18472925
http://dx.doi.org/10.1155/S0962935194000104
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