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Relevance of novel inflammatory markers in stroke-induced immunosuppression
BACKGROUND: Acute ischemic stroke (AIS) has a biphasic effect on the peripheral immune system. The initial inflammatory response is followed by systemic immunosuppression, referred to as stroke-induced immunosuppression (SIIS), leading to severe complications in stroke patients. We aimed to identify...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3948141/ https://www.ncbi.nlm.nih.gov/pubmed/24597828 http://dx.doi.org/10.1186/1471-2377-14-41 |
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author | Folyovich, András Biró, Enikő Orbán, Csaba Bajnok, Anna Varga, Viktória Béres-Molnár, Anna K Vásárhelyi, Barna Toldi, Gergely |
author_facet | Folyovich, András Biró, Enikő Orbán, Csaba Bajnok, Anna Varga, Viktória Béres-Molnár, Anna K Vásárhelyi, Barna Toldi, Gergely |
author_sort | Folyovich, András |
collection | PubMed |
description | BACKGROUND: Acute ischemic stroke (AIS) has a biphasic effect on the peripheral immune system. The initial inflammatory response is followed by systemic immunosuppression, referred to as stroke-induced immunosuppression (SIIS), leading to severe complications in stroke patients. We aimed to identify an inflammatory marker that best represents this biphasic immunological response after AIS. METHODS: We investigated the alteration of CRP, WBC, neutrophil count, suPAR levels, CD4+ CD25high Tregs, CD64+ and CD177+ neutrophils and monocytes in 12 acute ischemic stroke patients free of infection within 6 hours and one week after the insult. As controls, 14 age-matched healthy individuals were included. RESULTS: CRP, WBC and neutrophil count values were comparable in stroke patients within 6 hours and controls, however, they were elevated in stroke one week after the insult. suPAR levels were higher in both stroke groups compared to controls. The prevalence of CD64+ neutrophils was higher in stroke patients within 6 hours than in controls and it decreased in stroke one week after the insult below the level in controls (5.95 [5.41-8.75] % vs. 32.38 [9.21-43.93] % vs. 4.06 [1.73-6.77] %, p < 0.05). CONCLUSIONS: Our pilot study identified that the prevalence of CD64+ neutrophils may reflect a biphasic alteration of the immune response following AIS. Since its level decreases below baseline after one week of the CNS insult in stroke patients without infection, it might serve as a reliable candidate to identify the developing inflammatory response due to infection after stroke in the future. |
format | Online Article Text |
id | pubmed-3948141 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39481412014-03-11 Relevance of novel inflammatory markers in stroke-induced immunosuppression Folyovich, András Biró, Enikő Orbán, Csaba Bajnok, Anna Varga, Viktória Béres-Molnár, Anna K Vásárhelyi, Barna Toldi, Gergely BMC Neurol Research Article BACKGROUND: Acute ischemic stroke (AIS) has a biphasic effect on the peripheral immune system. The initial inflammatory response is followed by systemic immunosuppression, referred to as stroke-induced immunosuppression (SIIS), leading to severe complications in stroke patients. We aimed to identify an inflammatory marker that best represents this biphasic immunological response after AIS. METHODS: We investigated the alteration of CRP, WBC, neutrophil count, suPAR levels, CD4+ CD25high Tregs, CD64+ and CD177+ neutrophils and monocytes in 12 acute ischemic stroke patients free of infection within 6 hours and one week after the insult. As controls, 14 age-matched healthy individuals were included. RESULTS: CRP, WBC and neutrophil count values were comparable in stroke patients within 6 hours and controls, however, they were elevated in stroke one week after the insult. suPAR levels were higher in both stroke groups compared to controls. The prevalence of CD64+ neutrophils was higher in stroke patients within 6 hours than in controls and it decreased in stroke one week after the insult below the level in controls (5.95 [5.41-8.75] % vs. 32.38 [9.21-43.93] % vs. 4.06 [1.73-6.77] %, p < 0.05). CONCLUSIONS: Our pilot study identified that the prevalence of CD64+ neutrophils may reflect a biphasic alteration of the immune response following AIS. Since its level decreases below baseline after one week of the CNS insult in stroke patients without infection, it might serve as a reliable candidate to identify the developing inflammatory response due to infection after stroke in the future. BioMed Central 2014-03-06 /pmc/articles/PMC3948141/ /pubmed/24597828 http://dx.doi.org/10.1186/1471-2377-14-41 Text en Copyright © 2014 Folyovich et al.; licensee BioMed Central Ltd. 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 credited. |
spellingShingle | Research Article Folyovich, András Biró, Enikő Orbán, Csaba Bajnok, Anna Varga, Viktória Béres-Molnár, Anna K Vásárhelyi, Barna Toldi, Gergely Relevance of novel inflammatory markers in stroke-induced immunosuppression |
title | Relevance of novel inflammatory markers in stroke-induced immunosuppression |
title_full | Relevance of novel inflammatory markers in stroke-induced immunosuppression |
title_fullStr | Relevance of novel inflammatory markers in stroke-induced immunosuppression |
title_full_unstemmed | Relevance of novel inflammatory markers in stroke-induced immunosuppression |
title_short | Relevance of novel inflammatory markers in stroke-induced immunosuppression |
title_sort | relevance of novel inflammatory markers in stroke-induced immunosuppression |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3948141/ https://www.ncbi.nlm.nih.gov/pubmed/24597828 http://dx.doi.org/10.1186/1471-2377-14-41 |
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