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IL-17 production by CSF lymphocytes as a biomarker for cerebral vasculitis
OBJECTIVE: To explore the possibility of using interleukin-17 (IL-17) production by CD4+ T cells in the CSF as a potential biomarker for cerebral vasculitis in stroke patients. METHODS: In this consecutive case study, we performed prospective analysis of CSF and blood in patients admitted to a unive...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4841502/ https://www.ncbi.nlm.nih.gov/pubmed/27144213 http://dx.doi.org/10.1212/NXI.0000000000000214 |
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author | Thom, Vivien Schmid, Sabrina Gelderblom, Mathias Hackbusch, Romy Kolster, Manuela Schuster, Simon Thomalla, Götz Keminer, Oliver Pleß, Ole Bernreuther, Christian Glatzel, Markus Wegscheider, Karl Gerloff, Christian Magnus, Tim Tolosa, Eva |
author_facet | Thom, Vivien Schmid, Sabrina Gelderblom, Mathias Hackbusch, Romy Kolster, Manuela Schuster, Simon Thomalla, Götz Keminer, Oliver Pleß, Ole Bernreuther, Christian Glatzel, Markus Wegscheider, Karl Gerloff, Christian Magnus, Tim Tolosa, Eva |
author_sort | Thom, Vivien |
collection | PubMed |
description | OBJECTIVE: To explore the possibility of using interleukin-17 (IL-17) production by CD4+ T cells in the CSF as a potential biomarker for cerebral vasculitis in stroke patients. METHODS: In this consecutive case study, we performed prospective analysis of CSF and blood in patients admitted to a university medical center with symptoms of stroke and suspected cerebral vasculitis. Flow cytometry was performed for intracellular detection of inflammatory cytokines in peripheral blood lymphocytes and expanded T cells from CSF. RESULTS: CSF CD4+ lymphocytes from patients with cerebral vasculitis showed significantly higher levels of the proinflammatory cytokine IL-17 compared to patients with stroke not due to vasculitis or with other, noninflammatory neurologic diseases. There was no difference in the production of interferon-γ in the CSF and no overall differences in the relative frequencies of peripheral immune cells. CONCLUSIONS: Intracellular IL-17 in CSF cells is potentially useful in discriminating cerebral vasculitis as a rare cause in patients presenting with ischemic stroke. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that an increased proportion of IL-17-producing CD4+ cells in CSF of patients presenting with stroke symptoms is indicative of cerebral vasculitis (sensitivity 73%, 95% confidence interval [CI] 39–94%; specificity 100%, 95% CI 74%–100%). |
format | Online Article Text |
id | pubmed-4841502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-48415022016-05-03 IL-17 production by CSF lymphocytes as a biomarker for cerebral vasculitis Thom, Vivien Schmid, Sabrina Gelderblom, Mathias Hackbusch, Romy Kolster, Manuela Schuster, Simon Thomalla, Götz Keminer, Oliver Pleß, Ole Bernreuther, Christian Glatzel, Markus Wegscheider, Karl Gerloff, Christian Magnus, Tim Tolosa, Eva Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: To explore the possibility of using interleukin-17 (IL-17) production by CD4+ T cells in the CSF as a potential biomarker for cerebral vasculitis in stroke patients. METHODS: In this consecutive case study, we performed prospective analysis of CSF and blood in patients admitted to a university medical center with symptoms of stroke and suspected cerebral vasculitis. Flow cytometry was performed for intracellular detection of inflammatory cytokines in peripheral blood lymphocytes and expanded T cells from CSF. RESULTS: CSF CD4+ lymphocytes from patients with cerebral vasculitis showed significantly higher levels of the proinflammatory cytokine IL-17 compared to patients with stroke not due to vasculitis or with other, noninflammatory neurologic diseases. There was no difference in the production of interferon-γ in the CSF and no overall differences in the relative frequencies of peripheral immune cells. CONCLUSIONS: Intracellular IL-17 in CSF cells is potentially useful in discriminating cerebral vasculitis as a rare cause in patients presenting with ischemic stroke. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that an increased proportion of IL-17-producing CD4+ cells in CSF of patients presenting with stroke symptoms is indicative of cerebral vasculitis (sensitivity 73%, 95% confidence interval [CI] 39–94%; specificity 100%, 95% CI 74%–100%). Lippincott Williams & Wilkins 2016-03-21 /pmc/articles/PMC4841502/ /pubmed/27144213 http://dx.doi.org/10.1212/NXI.0000000000000214 Text en © 2016 American Academy of Neurology This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially. |
spellingShingle | Article Thom, Vivien Schmid, Sabrina Gelderblom, Mathias Hackbusch, Romy Kolster, Manuela Schuster, Simon Thomalla, Götz Keminer, Oliver Pleß, Ole Bernreuther, Christian Glatzel, Markus Wegscheider, Karl Gerloff, Christian Magnus, Tim Tolosa, Eva IL-17 production by CSF lymphocytes as a biomarker for cerebral vasculitis |
title | IL-17 production by CSF lymphocytes as a biomarker for cerebral vasculitis |
title_full | IL-17 production by CSF lymphocytes as a biomarker for cerebral vasculitis |
title_fullStr | IL-17 production by CSF lymphocytes as a biomarker for cerebral vasculitis |
title_full_unstemmed | IL-17 production by CSF lymphocytes as a biomarker for cerebral vasculitis |
title_short | IL-17 production by CSF lymphocytes as a biomarker for cerebral vasculitis |
title_sort | il-17 production by csf lymphocytes as a biomarker for cerebral vasculitis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4841502/ https://www.ncbi.nlm.nih.gov/pubmed/27144213 http://dx.doi.org/10.1212/NXI.0000000000000214 |
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