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Successful thrombolytic therapy is associated with increased granulocyte CD15 expression and reduced stroke‐induced immunosuppression

OBJECTIVES: Stroke‐induced immunosuppression (SIIS) increases the risk of poststroke infections. We aimed to determine whether failed versus successful thrombolytic therapy (TT) resulted in SIIS‐associated changes in peripheral granulocyte markers at 1 week following the insult. METHODS: We collecte...

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Autores principales: Béres‐Molnár, Katalin Anna, Czeti, Ágnes, Takács, Ferenc, Barna, Gábor, Kis, Dániel, Róka, Gabriella, Folyovich, András, Toldi, Gergely
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575610/
https://www.ncbi.nlm.nih.gov/pubmed/36111748
http://dx.doi.org/10.1002/brb3.2732
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author Béres‐Molnár, Katalin Anna
Czeti, Ágnes
Takács, Ferenc
Barna, Gábor
Kis, Dániel
Róka, Gabriella
Folyovich, András
Toldi, Gergely
author_facet Béres‐Molnár, Katalin Anna
Czeti, Ágnes
Takács, Ferenc
Barna, Gábor
Kis, Dániel
Róka, Gabriella
Folyovich, András
Toldi, Gergely
author_sort Béres‐Molnár, Katalin Anna
collection PubMed
description OBJECTIVES: Stroke‐induced immunosuppression (SIIS) increases the risk of poststroke infections. We aimed to determine whether failed versus successful thrombolytic therapy (TT) resulted in SIIS‐associated changes in peripheral granulocyte markers at 1 week following the insult. METHODS: We collected peripheral blood samples from 19 patients with acute ischemic stroke undergoing TT within 6 h after the onset of their first symptoms and 7 days after the insult. Age‐matched controls were sampled on one occasion. We compared the expression of CD15 and CD64 on monocytes, granulocytes, and lymphocytes using flow cytometry. RESULTS: The proportion of granulocytes and CD15+ granulocytes was comparable between controls and stroke patients at both time points. While the proportion of CD15bright granulocytes was also comparable, the mean fluorescence intensity (MFI) of CD15 on this subset was reduced in stroke patients by day 7 but was overall higher at both time points compared to controls. The MFI of CD15 on granulocytes was lower in stroke patients with failed TT than in those with successful TT 1 week after the insult. CONCLUSIONS: Our current results indicate that TT may not only acutely reduce the systemic inflammatory response following stroke but may also play a role in reversing SIIS at a later stage following the insult, as reflected by the higher expression of the CD15 marker on granulocytes following successful TT.
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spelling pubmed-95756102022-10-18 Successful thrombolytic therapy is associated with increased granulocyte CD15 expression and reduced stroke‐induced immunosuppression Béres‐Molnár, Katalin Anna Czeti, Ágnes Takács, Ferenc Barna, Gábor Kis, Dániel Róka, Gabriella Folyovich, András Toldi, Gergely Brain Behav Original Articles OBJECTIVES: Stroke‐induced immunosuppression (SIIS) increases the risk of poststroke infections. We aimed to determine whether failed versus successful thrombolytic therapy (TT) resulted in SIIS‐associated changes in peripheral granulocyte markers at 1 week following the insult. METHODS: We collected peripheral blood samples from 19 patients with acute ischemic stroke undergoing TT within 6 h after the onset of their first symptoms and 7 days after the insult. Age‐matched controls were sampled on one occasion. We compared the expression of CD15 and CD64 on monocytes, granulocytes, and lymphocytes using flow cytometry. RESULTS: The proportion of granulocytes and CD15+ granulocytes was comparable between controls and stroke patients at both time points. While the proportion of CD15bright granulocytes was also comparable, the mean fluorescence intensity (MFI) of CD15 on this subset was reduced in stroke patients by day 7 but was overall higher at both time points compared to controls. The MFI of CD15 on granulocytes was lower in stroke patients with failed TT than in those with successful TT 1 week after the insult. CONCLUSIONS: Our current results indicate that TT may not only acutely reduce the systemic inflammatory response following stroke but may also play a role in reversing SIIS at a later stage following the insult, as reflected by the higher expression of the CD15 marker on granulocytes following successful TT. John Wiley and Sons Inc. 2022-09-16 /pmc/articles/PMC9575610/ /pubmed/36111748 http://dx.doi.org/10.1002/brb3.2732 Text en © 2022 The Authors. Brain and Behavior published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Béres‐Molnár, Katalin Anna
Czeti, Ágnes
Takács, Ferenc
Barna, Gábor
Kis, Dániel
Róka, Gabriella
Folyovich, András
Toldi, Gergely
Successful thrombolytic therapy is associated with increased granulocyte CD15 expression and reduced stroke‐induced immunosuppression
title Successful thrombolytic therapy is associated with increased granulocyte CD15 expression and reduced stroke‐induced immunosuppression
title_full Successful thrombolytic therapy is associated with increased granulocyte CD15 expression and reduced stroke‐induced immunosuppression
title_fullStr Successful thrombolytic therapy is associated with increased granulocyte CD15 expression and reduced stroke‐induced immunosuppression
title_full_unstemmed Successful thrombolytic therapy is associated with increased granulocyte CD15 expression and reduced stroke‐induced immunosuppression
title_short Successful thrombolytic therapy is associated with increased granulocyte CD15 expression and reduced stroke‐induced immunosuppression
title_sort successful thrombolytic therapy is associated with increased granulocyte cd15 expression and reduced stroke‐induced immunosuppression
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9575610/
https://www.ncbi.nlm.nih.gov/pubmed/36111748
http://dx.doi.org/10.1002/brb3.2732
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