Cargando…

Temporal changes in regulatory T cell subsets defined by the transcription factor Helios in stroke and their potential role in stroke-associated infection: a prospective case–control study

BACKGROUND: Regulatory T cells (Tregs) are involved in the systemic immune response after ischemic stroke. However, their role remains unclear, and the effect appears to be both neuroprotective and detrimental. Treg suppressor function may result in immunodepression and promote stroke-associated inf...

Descripción completa

Detalles Bibliográficos
Autores principales: Lukasik, Maria, Telec, Magdalena, Kazmierski, Radoslaw, Wojtasz, Izabela, Andrzejewska-Gorczyńska, Natalia, Kociemba, Wojciech, Dworacki, Grzegorz, Kozubski, Wojciech P., Frydrychowicz, Magdalena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666369/
https://www.ncbi.nlm.nih.gov/pubmed/37996909
http://dx.doi.org/10.1186/s12974-023-02957-w
_version_ 1785148934554910720
author Lukasik, Maria
Telec, Magdalena
Kazmierski, Radoslaw
Wojtasz, Izabela
Andrzejewska-Gorczyńska, Natalia
Kociemba, Wojciech
Dworacki, Grzegorz
Kozubski, Wojciech P.
Frydrychowicz, Magdalena
author_facet Lukasik, Maria
Telec, Magdalena
Kazmierski, Radoslaw
Wojtasz, Izabela
Andrzejewska-Gorczyńska, Natalia
Kociemba, Wojciech
Dworacki, Grzegorz
Kozubski, Wojciech P.
Frydrychowicz, Magdalena
author_sort Lukasik, Maria
collection PubMed
description BACKGROUND: Regulatory T cells (Tregs) are involved in the systemic immune response after ischemic stroke. However, their role remains unclear, and the effect appears to be both neuroprotective and detrimental. Treg suppressor function may result in immunodepression and promote stroke-associated infection (SAI). Thus we assume that the bidirectional effects of Tregs may be in part attributed to the intracellular transcription factor Helios. Tregs with Helios expression (H+ Tregs) constitute 70–90% of all Treg cells and more frequently than Helios-negative Tregs (H− Tregs) express molecules recognized as markers of Tregs with suppressor abilities. METHODS AND RESULTS: We prospectively assessed the circulating Treg population with flow cytometry in 52 subjects on days 1, 3, 10 and 90 after ischemic stroke and we compared the results with those obtained in concurrent age-, sex- and vascular risk factor-matched controls. At all studied time points the percentage of H+ Tregs decreased in stroke subjects—D1: 69.1% p < 0.0001; D3: 62.5% (49.6–76.6), p < 0.0001; D10: 60.9% (56.5–72.9), p < 0.0001; D90: 79.2% (50.2–91.7), p = 0.014 vs. controls: 92.7% (81.9–97.0) and the percentage of H− Tregs increased accordingly. In patients with SAI the percentage of pro-suppressor H+ Tregs on post-stroke day 3 was higher than in those without infection (p = 0.03). After adjustment for confounders, the percentage of H+ Tregs on day 3 independently correlated with SAI [OR 1.29; CI 95%: 1.08–1.27); p = 0.02]. Although the percentage of H+ Tregs on day 3 correlated positively with NIHSS score on day 90 (rS = 0.62; p < 0.01) and the infarct volume at day 90 (rS = 0.58; p < 0.05), in regression analysis it was not an independent risk factor. CONCLUSIONS: On the first day after stroke the proportion of H+ vs. H− Tregs changes in favor of pro-inflammatory H− Tregs, and this shift continues toward normalization when assessed on day 90. A higher percentage of pro-suppressive H+ Tregs on day 3 independently correlates with SAI and is associated positively with NIHSS score, but it does not independently affect the outcome and stroke area in the convalescent phase of stroke. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12974-023-02957-w.
format Online
Article
Text
id pubmed-10666369
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-106663692023-11-23 Temporal changes in regulatory T cell subsets defined by the transcription factor Helios in stroke and their potential role in stroke-associated infection: a prospective case–control study Lukasik, Maria Telec, Magdalena Kazmierski, Radoslaw Wojtasz, Izabela Andrzejewska-Gorczyńska, Natalia Kociemba, Wojciech Dworacki, Grzegorz Kozubski, Wojciech P. Frydrychowicz, Magdalena J Neuroinflammation Research BACKGROUND: Regulatory T cells (Tregs) are involved in the systemic immune response after ischemic stroke. However, their role remains unclear, and the effect appears to be both neuroprotective and detrimental. Treg suppressor function may result in immunodepression and promote stroke-associated infection (SAI). Thus we assume that the bidirectional effects of Tregs may be in part attributed to the intracellular transcription factor Helios. Tregs with Helios expression (H+ Tregs) constitute 70–90% of all Treg cells and more frequently than Helios-negative Tregs (H− Tregs) express molecules recognized as markers of Tregs with suppressor abilities. METHODS AND RESULTS: We prospectively assessed the circulating Treg population with flow cytometry in 52 subjects on days 1, 3, 10 and 90 after ischemic stroke and we compared the results with those obtained in concurrent age-, sex- and vascular risk factor-matched controls. At all studied time points the percentage of H+ Tregs decreased in stroke subjects—D1: 69.1% p < 0.0001; D3: 62.5% (49.6–76.6), p < 0.0001; D10: 60.9% (56.5–72.9), p < 0.0001; D90: 79.2% (50.2–91.7), p = 0.014 vs. controls: 92.7% (81.9–97.0) and the percentage of H− Tregs increased accordingly. In patients with SAI the percentage of pro-suppressor H+ Tregs on post-stroke day 3 was higher than in those without infection (p = 0.03). After adjustment for confounders, the percentage of H+ Tregs on day 3 independently correlated with SAI [OR 1.29; CI 95%: 1.08–1.27); p = 0.02]. Although the percentage of H+ Tregs on day 3 correlated positively with NIHSS score on day 90 (rS = 0.62; p < 0.01) and the infarct volume at day 90 (rS = 0.58; p < 0.05), in regression analysis it was not an independent risk factor. CONCLUSIONS: On the first day after stroke the proportion of H+ vs. H− Tregs changes in favor of pro-inflammatory H− Tregs, and this shift continues toward normalization when assessed on day 90. A higher percentage of pro-suppressive H+ Tregs on day 3 independently correlates with SAI and is associated positively with NIHSS score, but it does not independently affect the outcome and stroke area in the convalescent phase of stroke. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12974-023-02957-w. BioMed Central 2023-11-23 /pmc/articles/PMC10666369/ /pubmed/37996909 http://dx.doi.org/10.1186/s12974-023-02957-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Lukasik, Maria
Telec, Magdalena
Kazmierski, Radoslaw
Wojtasz, Izabela
Andrzejewska-Gorczyńska, Natalia
Kociemba, Wojciech
Dworacki, Grzegorz
Kozubski, Wojciech P.
Frydrychowicz, Magdalena
Temporal changes in regulatory T cell subsets defined by the transcription factor Helios in stroke and their potential role in stroke-associated infection: a prospective case–control study
title Temporal changes in regulatory T cell subsets defined by the transcription factor Helios in stroke and their potential role in stroke-associated infection: a prospective case–control study
title_full Temporal changes in regulatory T cell subsets defined by the transcription factor Helios in stroke and their potential role in stroke-associated infection: a prospective case–control study
title_fullStr Temporal changes in regulatory T cell subsets defined by the transcription factor Helios in stroke and their potential role in stroke-associated infection: a prospective case–control study
title_full_unstemmed Temporal changes in regulatory T cell subsets defined by the transcription factor Helios in stroke and their potential role in stroke-associated infection: a prospective case–control study
title_short Temporal changes in regulatory T cell subsets defined by the transcription factor Helios in stroke and their potential role in stroke-associated infection: a prospective case–control study
title_sort temporal changes in regulatory t cell subsets defined by the transcription factor helios in stroke and their potential role in stroke-associated infection: a prospective case–control study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666369/
https://www.ncbi.nlm.nih.gov/pubmed/37996909
http://dx.doi.org/10.1186/s12974-023-02957-w
work_keys_str_mv AT lukasikmaria temporalchangesinregulatorytcellsubsetsdefinedbythetranscriptionfactorheliosinstrokeandtheirpotentialroleinstrokeassociatedinfectionaprospectivecasecontrolstudy
AT telecmagdalena temporalchangesinregulatorytcellsubsetsdefinedbythetranscriptionfactorheliosinstrokeandtheirpotentialroleinstrokeassociatedinfectionaprospectivecasecontrolstudy
AT kazmierskiradoslaw temporalchangesinregulatorytcellsubsetsdefinedbythetranscriptionfactorheliosinstrokeandtheirpotentialroleinstrokeassociatedinfectionaprospectivecasecontrolstudy
AT wojtaszizabela temporalchangesinregulatorytcellsubsetsdefinedbythetranscriptionfactorheliosinstrokeandtheirpotentialroleinstrokeassociatedinfectionaprospectivecasecontrolstudy
AT andrzejewskagorczynskanatalia temporalchangesinregulatorytcellsubsetsdefinedbythetranscriptionfactorheliosinstrokeandtheirpotentialroleinstrokeassociatedinfectionaprospectivecasecontrolstudy
AT kociembawojciech temporalchangesinregulatorytcellsubsetsdefinedbythetranscriptionfactorheliosinstrokeandtheirpotentialroleinstrokeassociatedinfectionaprospectivecasecontrolstudy
AT dworackigrzegorz temporalchangesinregulatorytcellsubsetsdefinedbythetranscriptionfactorheliosinstrokeandtheirpotentialroleinstrokeassociatedinfectionaprospectivecasecontrolstudy
AT kozubskiwojciechp temporalchangesinregulatorytcellsubsetsdefinedbythetranscriptionfactorheliosinstrokeandtheirpotentialroleinstrokeassociatedinfectionaprospectivecasecontrolstudy
AT frydrychowiczmagdalena temporalchangesinregulatorytcellsubsetsdefinedbythetranscriptionfactorheliosinstrokeandtheirpotentialroleinstrokeassociatedinfectionaprospectivecasecontrolstudy