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Decrease of perforin positive CD3(+)γδ-T cells in patients with obstructive sleep disordered breathing
INTRODUCTION: Sleep related breathing disorders (SRBD) cause sleep fragmentation, intermittent hypoxia or a combination of both leading to homeostasis perturbations, including in the immune system. We investigated whether SRBD patients with or without intermittent hypoxia show substantial difference...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835055/ https://www.ncbi.nlm.nih.gov/pubmed/29247296 http://dx.doi.org/10.1007/s11325-017-1602-6 |
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author | Staats, Richard Rodrigues, Raquel Barros, André Bacelar-Nicolau, Leonor Aguiar, Margarida Fernandes, Dina Moreira, Susana Simões, André Silva-Santos, Bruno Rodrigues, João Valença Barbara, Cristina de Almeida, António Bugalho Moita, Luis Ferreira |
author_facet | Staats, Richard Rodrigues, Raquel Barros, André Bacelar-Nicolau, Leonor Aguiar, Margarida Fernandes, Dina Moreira, Susana Simões, André Silva-Santos, Bruno Rodrigues, João Valença Barbara, Cristina de Almeida, António Bugalho Moita, Luis Ferreira |
author_sort | Staats, Richard |
collection | PubMed |
description | INTRODUCTION: Sleep related breathing disorders (SRBD) cause sleep fragmentation, intermittent hypoxia or a combination of both leading to homeostasis perturbations, including in the immune system. We investigated whether SRBD patients with or without intermittent hypoxia show substantial differences in perforin and granzyme-B positive peripheral blood lymphocytes. METHODS: A total of 87 subjects were included and distributed as follows: 24 controls (C), 19 patients with respiratory effort related arousals due to increased upper airway resistance (UAR) without hypoxic events, 24 obese patients with obstructive sleep apnea (OSA) (oOSA), and 20 without obesity (noOSA). After polysomnographic recording, we analyzed in fasting blood samples routine hematologic and biochemical parameters and the percentage of lymphocytes containing the proteins perforin and granzyme-B (GrB). Kruskal-Wallis tests and a posteriori multiple comparisons were applied for statistical analysis of results. RESULTS: Perforin-positive γδ-cells revealed significant differences between groups (p = 0.017), especially between the Control group and the oOSA (p-value = 0.04); the remaining SRBD groups also showed differences from the control (C vs UAR: p = 0.08; C vs noOSA = 0.09), but they did not raise to statistical significance. There were no differences among the SRBD groups. Granzyme-B cells were decreased in SRBD patients, but the differences were not statistically significant. No additional statistical significant result was found in the other investigated lymphocyte subsets. CONCLUSIONS: Obstructive sleep-disordered breathing is associated with a decrease in perforin-positive CD3(+)γδ-T cells. Although this finding was detected in lean patients without intermittent hypoxia, the reduction was only statistically significant in obese patients with severe OSA. Because CD3(+)γδ-T cells play an important role in the control of tumor cells, our findings are directly relevant for the study of the association of OSA and cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11325-017-1602-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5835055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-58350552018-03-09 Decrease of perforin positive CD3(+)γδ-T cells in patients with obstructive sleep disordered breathing Staats, Richard Rodrigues, Raquel Barros, André Bacelar-Nicolau, Leonor Aguiar, Margarida Fernandes, Dina Moreira, Susana Simões, André Silva-Santos, Bruno Rodrigues, João Valença Barbara, Cristina de Almeida, António Bugalho Moita, Luis Ferreira Sleep Breath Basic Science • Original Article INTRODUCTION: Sleep related breathing disorders (SRBD) cause sleep fragmentation, intermittent hypoxia or a combination of both leading to homeostasis perturbations, including in the immune system. We investigated whether SRBD patients with or without intermittent hypoxia show substantial differences in perforin and granzyme-B positive peripheral blood lymphocytes. METHODS: A total of 87 subjects were included and distributed as follows: 24 controls (C), 19 patients with respiratory effort related arousals due to increased upper airway resistance (UAR) without hypoxic events, 24 obese patients with obstructive sleep apnea (OSA) (oOSA), and 20 without obesity (noOSA). After polysomnographic recording, we analyzed in fasting blood samples routine hematologic and biochemical parameters and the percentage of lymphocytes containing the proteins perforin and granzyme-B (GrB). Kruskal-Wallis tests and a posteriori multiple comparisons were applied for statistical analysis of results. RESULTS: Perforin-positive γδ-cells revealed significant differences between groups (p = 0.017), especially between the Control group and the oOSA (p-value = 0.04); the remaining SRBD groups also showed differences from the control (C vs UAR: p = 0.08; C vs noOSA = 0.09), but they did not raise to statistical significance. There were no differences among the SRBD groups. Granzyme-B cells were decreased in SRBD patients, but the differences were not statistically significant. No additional statistical significant result was found in the other investigated lymphocyte subsets. CONCLUSIONS: Obstructive sleep-disordered breathing is associated with a decrease in perforin-positive CD3(+)γδ-T cells. Although this finding was detected in lean patients without intermittent hypoxia, the reduction was only statistically significant in obese patients with severe OSA. Because CD3(+)γδ-T cells play an important role in the control of tumor cells, our findings are directly relevant for the study of the association of OSA and cancer. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11325-017-1602-6) contains supplementary material, which is available to authorized users. Springer International Publishing 2017-12-15 2018 /pmc/articles/PMC5835055/ /pubmed/29247296 http://dx.doi.org/10.1007/s11325-017-1602-6 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Basic Science • Original Article Staats, Richard Rodrigues, Raquel Barros, André Bacelar-Nicolau, Leonor Aguiar, Margarida Fernandes, Dina Moreira, Susana Simões, André Silva-Santos, Bruno Rodrigues, João Valença Barbara, Cristina de Almeida, António Bugalho Moita, Luis Ferreira Decrease of perforin positive CD3(+)γδ-T cells in patients with obstructive sleep disordered breathing |
title | Decrease of perforin positive CD3(+)γδ-T cells in patients with obstructive sleep disordered breathing |
title_full | Decrease of perforin positive CD3(+)γδ-T cells in patients with obstructive sleep disordered breathing |
title_fullStr | Decrease of perforin positive CD3(+)γδ-T cells in patients with obstructive sleep disordered breathing |
title_full_unstemmed | Decrease of perforin positive CD3(+)γδ-T cells in patients with obstructive sleep disordered breathing |
title_short | Decrease of perforin positive CD3(+)γδ-T cells in patients with obstructive sleep disordered breathing |
title_sort | decrease of perforin positive cd3(+)γδ-t cells in patients with obstructive sleep disordered breathing |
topic | Basic Science • Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835055/ https://www.ncbi.nlm.nih.gov/pubmed/29247296 http://dx.doi.org/10.1007/s11325-017-1602-6 |
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