The post sepsis-induced expansion and enhanced function of regulatory T cells create an environment to potentiate tumor growth
One of the more insidious outcomes of patients who survive severe sepsis is profound immunosuppression. In this study, we addressed the hypothesis that post septic immune defects were due, in part, to the presence and/or expansion of regulatory T cells (Tregs). After recovery from severe sepsis, mice exhibited significantly higher numbers of Tregs, which exerted greater in vitro suppressive activity compared with controls. The expansion of Tregs was not limited to CD25(+) cells, because Foxp3 expression was also detected in CD25(-) cells from post septic mice. This latter group exhibited a significant increase of chromatin remodeling at the Foxp3 promoter, because a marked increase in acetylation at H3K9 was associated with an increase in Foxp3 transcription. Post septic splenic dendritic cells promoted Treg conversion in vitro. Using a solid tumor model to explore the function of Tregs in an in vivo setting, we found post septic mice showed an increase in tumor growth compared with sham-treated mice with a syngeneic tumor model. This observation could mechanistically be related to the ability of post septic Tregs to impair the antitumor response mediated by CD8(+) T cells. Together, these data show that the post septic immune system obstructs tumor immunosurveillance, in part, by augmented Treg expansion and function.
| Errataetall: |
CommentIn: Blood. 2010 Jun 3;115(22):4324-5. - PMID 20522717 |
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| Medienart: |
E-Artikel |
| Erscheinungsjahr: |
2010 |
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| Erschienen: |
2010 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:115 |
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| Enthalten in: |
Blood - 115(2010), 22 vom: 03. Juni, Seite 4403-11 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Cavassani, Karen A [VerfasserIn] |
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| Links: |
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| Themen: |
Forkhead Transcription Factors |
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| Anmerkungen: |
Date Completed 23.06.2010 Date Revised 31.03.2022 published: Print-Electronic CommentIn: Blood. 2010 Jun 3;115(22):4324-5. - PMID 20522717 Citation Status MEDLINE |
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| doi: |
10.1182/blood-2009-09-241083 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM194858197 |
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| 245 | 1 | 4 | |a The post sepsis-induced expansion and enhanced function of regulatory T cells create an environment to potentiate tumor growth |
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| 500 | |a CommentIn: Blood. 2010 Jun 3;115(22):4324-5. - PMID 20522717 | ||
| 500 | |a Citation Status MEDLINE | ||
| 520 | |a One of the more insidious outcomes of patients who survive severe sepsis is profound immunosuppression. In this study, we addressed the hypothesis that post septic immune defects were due, in part, to the presence and/or expansion of regulatory T cells (Tregs). After recovery from severe sepsis, mice exhibited significantly higher numbers of Tregs, which exerted greater in vitro suppressive activity compared with controls. The expansion of Tregs was not limited to CD25(+) cells, because Foxp3 expression was also detected in CD25(-) cells from post septic mice. This latter group exhibited a significant increase of chromatin remodeling at the Foxp3 promoter, because a marked increase in acetylation at H3K9 was associated with an increase in Foxp3 transcription. Post septic splenic dendritic cells promoted Treg conversion in vitro. Using a solid tumor model to explore the function of Tregs in an in vivo setting, we found post septic mice showed an increase in tumor growth compared with sham-treated mice with a syngeneic tumor model. This observation could mechanistically be related to the ability of post septic Tregs to impair the antitumor response mediated by CD8(+) T cells. Together, these data show that the post septic immune system obstructs tumor immunosurveillance, in part, by augmented Treg expansion and function | ||
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| 700 | 1 | |a Kunkel, Steven L |e verfasserin |4 aut | |
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