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IL-17 and IL-23 levels in patients with early-stage chronic lymphocytic leukemia
OBJECTIVE: Cytokines produced by bone marrow mesenchymal stem cells are important components of the tumor microenvironment in chronic lymphocytic leukemia (CLL). The roles of IL-17 and IL-23 in both autoimmune diseases and tumor growth have been demonstrated. The role of the IL-17/23 axis in apoptos...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Kare Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881423/ https://www.ncbi.nlm.nih.gov/pubmed/33623869 http://dx.doi.org/10.14744/nci.2020.02997 |
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author | Bankir, Mehmet Acik, Didar Yanardag |
author_facet | Bankir, Mehmet Acik, Didar Yanardag |
author_sort | Bankir, Mehmet |
collection | PubMed |
description | OBJECTIVE: Cytokines produced by bone marrow mesenchymal stem cells are important components of the tumor microenvironment in chronic lymphocytic leukemia (CLL). The roles of IL-17 and IL-23 in both autoimmune diseases and tumor growth have been demonstrated. The role of the IL-17/23 axis in apoptosis has also been demonstrated in studies. Autoimmune cytopenias are common in CLL. In this study, we aimed to compare IL-17/IL-23 levels in early-stage CLL patients with healthy controls. METHODS: After obtaining ethical approval from the local ethics committee, 22 patients with early-stage chronic lymphocytic leukemia and 21 healthy control groups were included in this study. IL-17 and IL-23 were analyzed using the enzyme-linked immunosorbent assay method. RESULTS: The findings showed that the median IL-23 level was lower in men in the chronic lymphocytic leukemia group than women. There was a positive correlation between IL-17 and IL-23 levels in both the control group and the chronic lymphocytic leukemia group. There was no significant correlation between stage and IL-17 and IL-23 levels in chronic lymphocytic leukemia patients. CONCLUSION: Results of studies conducted on IL-17 and/or IL-23 in chronic lymphocytic leukemia in the literature are not consistent. These inconsistent results can be explained by the fact that the immune system develops differently in each individual due to environmental factors, past infections, intestinal flora, vaccines, ethnicity, and even gender. Therefore, it can be hypothesized that the development and application of personalized immunotherapy strategies instead of standard therapy in chronic lymphocytic leukemia may increase therapeutic success rates. |
format | Online Article Text |
id | pubmed-7881423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Kare Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-78814232021-02-22 IL-17 and IL-23 levels in patients with early-stage chronic lymphocytic leukemia Bankir, Mehmet Acik, Didar Yanardag North Clin Istanb Original Article OBJECTIVE: Cytokines produced by bone marrow mesenchymal stem cells are important components of the tumor microenvironment in chronic lymphocytic leukemia (CLL). The roles of IL-17 and IL-23 in both autoimmune diseases and tumor growth have been demonstrated. The role of the IL-17/23 axis in apoptosis has also been demonstrated in studies. Autoimmune cytopenias are common in CLL. In this study, we aimed to compare IL-17/IL-23 levels in early-stage CLL patients with healthy controls. METHODS: After obtaining ethical approval from the local ethics committee, 22 patients with early-stage chronic lymphocytic leukemia and 21 healthy control groups were included in this study. IL-17 and IL-23 were analyzed using the enzyme-linked immunosorbent assay method. RESULTS: The findings showed that the median IL-23 level was lower in men in the chronic lymphocytic leukemia group than women. There was a positive correlation between IL-17 and IL-23 levels in both the control group and the chronic lymphocytic leukemia group. There was no significant correlation between stage and IL-17 and IL-23 levels in chronic lymphocytic leukemia patients. CONCLUSION: Results of studies conducted on IL-17 and/or IL-23 in chronic lymphocytic leukemia in the literature are not consistent. These inconsistent results can be explained by the fact that the immune system develops differently in each individual due to environmental factors, past infections, intestinal flora, vaccines, ethnicity, and even gender. Therefore, it can be hypothesized that the development and application of personalized immunotherapy strategies instead of standard therapy in chronic lymphocytic leukemia may increase therapeutic success rates. Kare Publishing 2020-11-20 /pmc/articles/PMC7881423/ /pubmed/33623869 http://dx.doi.org/10.14744/nci.2020.02997 Text en Copyright: © 2021 by Istanbul Northern Anatolian Association of Public Hospitals http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License |
spellingShingle | Original Article Bankir, Mehmet Acik, Didar Yanardag IL-17 and IL-23 levels in patients with early-stage chronic lymphocytic leukemia |
title | IL-17 and IL-23 levels in patients with early-stage chronic lymphocytic leukemia |
title_full | IL-17 and IL-23 levels in patients with early-stage chronic lymphocytic leukemia |
title_fullStr | IL-17 and IL-23 levels in patients with early-stage chronic lymphocytic leukemia |
title_full_unstemmed | IL-17 and IL-23 levels in patients with early-stage chronic lymphocytic leukemia |
title_short | IL-17 and IL-23 levels in patients with early-stage chronic lymphocytic leukemia |
title_sort | il-17 and il-23 levels in patients with early-stage chronic lymphocytic leukemia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881423/ https://www.ncbi.nlm.nih.gov/pubmed/33623869 http://dx.doi.org/10.14744/nci.2020.02997 |
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