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IL-23 Gene Expression in PBMCs of Patients with Coronary Artery Disease
Objective: Both adaptive and innate immune systems are involved in coronary artery disease (CAD). The aim of this study was to evaluate TH17 cytokines expression profiles in un-stimulated peripheral blood lymphocytes (PBMCs) of patients with coronary artery disease. Methods: Expression profiles of I...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810777/ https://www.ncbi.nlm.nih.gov/pubmed/23023190 http://dx.doi.org/10.3233/DMA-2012-00933 |
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author | Khojasteh-Fard, Maryam Abolhalaj, Milad Amiri, Parvin Zaki, Majid Taheri, Zahra Qorbani, Mostafa Bazzaz, Javad Tavakkoly Amoli, Mahsa M. |
author_facet | Khojasteh-Fard, Maryam Abolhalaj, Milad Amiri, Parvin Zaki, Majid Taheri, Zahra Qorbani, Mostafa Bazzaz, Javad Tavakkoly Amoli, Mahsa M. |
author_sort | Khojasteh-Fard, Maryam |
collection | PubMed |
description | Objective: Both adaptive and innate immune systems are involved in coronary artery disease (CAD). The aim of this study was to evaluate TH17 cytokines expression profiles in un-stimulated peripheral blood lymphocytes (PBMCs) of patients with coronary artery disease. Methods: Expression profiles of IL-17, IL-23, and TGF-β1 were determined in individuals with and without CAD using Real-time PCR. Results: A significant decrease in IL-23 gene expression in un-stimulated PBMCs of patients with CAD compared to those without CAD was found (p=0.003, OR=0.045, 95% CI: 0.006–0.355). Conclusion: Our data reinforce the potential role of the IL-23 as a critical regulatory molecule that bridges the innate and adaptive arms of the immune system in the complex mechanisms associated with the development of atherosclerosis. |
format | Online Article Text |
id | pubmed-3810777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38107772013-12-10 IL-23 Gene Expression in PBMCs of Patients with Coronary Artery Disease Khojasteh-Fard, Maryam Abolhalaj, Milad Amiri, Parvin Zaki, Majid Taheri, Zahra Qorbani, Mostafa Bazzaz, Javad Tavakkoly Amoli, Mahsa M. Dis Markers Other Objective: Both adaptive and innate immune systems are involved in coronary artery disease (CAD). The aim of this study was to evaluate TH17 cytokines expression profiles in un-stimulated peripheral blood lymphocytes (PBMCs) of patients with coronary artery disease. Methods: Expression profiles of IL-17, IL-23, and TGF-β1 were determined in individuals with and without CAD using Real-time PCR. Results: A significant decrease in IL-23 gene expression in un-stimulated PBMCs of patients with CAD compared to those without CAD was found (p=0.003, OR=0.045, 95% CI: 0.006–0.355). Conclusion: Our data reinforce the potential role of the IL-23 as a critical regulatory molecule that bridges the innate and adaptive arms of the immune system in the complex mechanisms associated with the development of atherosclerosis. IOS Press 2012 2012-12-05 /pmc/articles/PMC3810777/ /pubmed/23023190 http://dx.doi.org/10.3233/DMA-2012-00933 Text en Copyright © 2012 Hindawi Publishing Corporation. |
spellingShingle | Other Khojasteh-Fard, Maryam Abolhalaj, Milad Amiri, Parvin Zaki, Majid Taheri, Zahra Qorbani, Mostafa Bazzaz, Javad Tavakkoly Amoli, Mahsa M. IL-23 Gene Expression in PBMCs of Patients with Coronary Artery Disease |
title | IL-23 Gene Expression in PBMCs of Patients with Coronary Artery Disease |
title_full | IL-23 Gene Expression in PBMCs of Patients with Coronary Artery Disease |
title_fullStr | IL-23 Gene Expression in PBMCs of Patients with Coronary Artery Disease |
title_full_unstemmed | IL-23 Gene Expression in PBMCs of Patients with Coronary Artery Disease |
title_short | IL-23 Gene Expression in PBMCs of Patients with Coronary Artery Disease |
title_sort | il-23 gene expression in pbmcs of patients with coronary artery disease |
topic | Other |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810777/ https://www.ncbi.nlm.nih.gov/pubmed/23023190 http://dx.doi.org/10.3233/DMA-2012-00933 |
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