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Endotoxin tolerance modulates TREG and TH17 lymphocytes protecting septic mice
Background: Tolerance induces a regulated immune response to infection. We hypothesized that tolerance induction modulated profile of T regulatory cell (Treg) and T lymphocyte 17 (Th17) cells and is related cytokine released in septic animals. Methods: Male black C57/6 mice received subcutaneous (s....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544402/ https://www.ncbi.nlm.nih.gov/pubmed/31191818 http://dx.doi.org/10.18632/oncotarget.26919 |
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author | Andrade, Mariana M.C. Ariga, Suely S.K. Barbeiro, Denise F. Barbeiro, Hermes V. Pimentel, Rosangela N. Petroni, Ricardo C. Soriano, Francisco G. |
author_facet | Andrade, Mariana M.C. Ariga, Suely S.K. Barbeiro, Denise F. Barbeiro, Hermes V. Pimentel, Rosangela N. Petroni, Ricardo C. Soriano, Francisco G. |
author_sort | Andrade, Mariana M.C. |
collection | PubMed |
description | Background: Tolerance induces a regulated immune response to infection. We hypothesized that tolerance induction modulated profile of T regulatory cell (Treg) and T lymphocyte 17 (Th17) cells and is related cytokine released in septic animals. Methods: Male black C57/6 mice received subcutaneous (s.c.) injections of lipopolysaccharide (LPS) (1 mg/kg) for 5 days, on day 8(th) was made cecal ligation and puncture (CLP). Blood and spleen tissue were collected for cell analysis and cytokines measurements. Results: Cytokines (interleukin 2 (IL-2), interleukin (IL-6), transforming growth factor β (TGF-β) and interferon γ (INF-γ)) related to Treg and Th17 stimulation were elevated in the spleen of tolerant animals compared to sham. Treg and Th17 lymphocytes showed an increased amount in blood (Treg: 920 ± 84 cells vs. 1946 ± 65 cells, sham vs. tolerant; Th17:38321± 1954 cells vs. 43526 ± 7623 cells, sham vs. tolerant) and spleen (Treg: 5947 ± 273 cells vs. 16521 ± 486 cells, sham vs. tolerant; Th17: 26543 ± 2944 cells vs. 64567 ± 5523 cells, sham vs. tolerant). Treg (135±23 cells) and Th17 (1590 ± 256 cells) cells were reduced in blood of septic animals compared to sham, while CLP tolerant animals presented an increasing number of these cells. Lymphocyte Th17IL6+ were elevated in tolerant and CLP tolerant animals in the blood compared to sham. Conclusion: LPS tolerance was associated with increasing population of Treg and Th17. LPS tolerance reduces the hyper inflammatory response with immunoregulation exerted by Treg and Th17 cells protecting from septic damage. |
format | Online Article Text |
id | pubmed-6544402 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-65444022019-06-12 Endotoxin tolerance modulates TREG and TH17 lymphocytes protecting septic mice Andrade, Mariana M.C. Ariga, Suely S.K. Barbeiro, Denise F. Barbeiro, Hermes V. Pimentel, Rosangela N. Petroni, Ricardo C. Soriano, Francisco G. Oncotarget Research Paper: Immunology Background: Tolerance induces a regulated immune response to infection. We hypothesized that tolerance induction modulated profile of T regulatory cell (Treg) and T lymphocyte 17 (Th17) cells and is related cytokine released in septic animals. Methods: Male black C57/6 mice received subcutaneous (s.c.) injections of lipopolysaccharide (LPS) (1 mg/kg) for 5 days, on day 8(th) was made cecal ligation and puncture (CLP). Blood and spleen tissue were collected for cell analysis and cytokines measurements. Results: Cytokines (interleukin 2 (IL-2), interleukin (IL-6), transforming growth factor β (TGF-β) and interferon γ (INF-γ)) related to Treg and Th17 stimulation were elevated in the spleen of tolerant animals compared to sham. Treg and Th17 lymphocytes showed an increased amount in blood (Treg: 920 ± 84 cells vs. 1946 ± 65 cells, sham vs. tolerant; Th17:38321± 1954 cells vs. 43526 ± 7623 cells, sham vs. tolerant) and spleen (Treg: 5947 ± 273 cells vs. 16521 ± 486 cells, sham vs. tolerant; Th17: 26543 ± 2944 cells vs. 64567 ± 5523 cells, sham vs. tolerant). Treg (135±23 cells) and Th17 (1590 ± 256 cells) cells were reduced in blood of septic animals compared to sham, while CLP tolerant animals presented an increasing number of these cells. Lymphocyte Th17IL6+ were elevated in tolerant and CLP tolerant animals in the blood compared to sham. Conclusion: LPS tolerance was associated with increasing population of Treg and Th17. LPS tolerance reduces the hyper inflammatory response with immunoregulation exerted by Treg and Th17 cells protecting from septic damage. Impact Journals LLC 2019-05-28 /pmc/articles/PMC6544402/ /pubmed/31191818 http://dx.doi.org/10.18632/oncotarget.26919 Text en Copyright: © 2019 Andrade et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper: Immunology Andrade, Mariana M.C. Ariga, Suely S.K. Barbeiro, Denise F. Barbeiro, Hermes V. Pimentel, Rosangela N. Petroni, Ricardo C. Soriano, Francisco G. Endotoxin tolerance modulates TREG and TH17 lymphocytes protecting septic mice |
title | Endotoxin tolerance modulates TREG and TH17 lymphocytes protecting septic mice |
title_full | Endotoxin tolerance modulates TREG and TH17 lymphocytes protecting septic mice |
title_fullStr | Endotoxin tolerance modulates TREG and TH17 lymphocytes protecting septic mice |
title_full_unstemmed | Endotoxin tolerance modulates TREG and TH17 lymphocytes protecting septic mice |
title_short | Endotoxin tolerance modulates TREG and TH17 lymphocytes protecting septic mice |
title_sort | endotoxin tolerance modulates treg and th17 lymphocytes protecting septic mice |
topic | Research Paper: Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544402/ https://www.ncbi.nlm.nih.gov/pubmed/31191818 http://dx.doi.org/10.18632/oncotarget.26919 |
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