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Blood CD33(+)HLA-DR(−) myeloid-derived suppressor cells are increased with age and a history of cancer
As we age, the composition of our peripheral leukocytes changes dramatically. Many of these alterations contribute to the general immune dysfunction that burdens the elderly, which in turn, contributes to increased susceptibility to disease. MDSCs represent a heterogeneous population of immunosuppre...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Society for Leukocyte Biology
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701116/ https://www.ncbi.nlm.nih.gov/pubmed/23341539 http://dx.doi.org/10.1189/jlb.0912461 |
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author | Verschoor, Chris P. Johnstone, Jennie Millar, Jamie Dorrington, Michael G. Habibagahi, Mojtaba Lelic, Alina Loeb, Mark Bramson, Jonathan L. Bowdish, Dawn M. E. |
author_facet | Verschoor, Chris P. Johnstone, Jennie Millar, Jamie Dorrington, Michael G. Habibagahi, Mojtaba Lelic, Alina Loeb, Mark Bramson, Jonathan L. Bowdish, Dawn M. E. |
author_sort | Verschoor, Chris P. |
collection | PubMed |
description | As we age, the composition of our peripheral leukocytes changes dramatically. Many of these alterations contribute to the general immune dysfunction that burdens the elderly, which in turn, contributes to increased susceptibility to disease. MDSCs represent a heterogeneous population of immunosuppressive leukocytes that are elevated in the peripheral blood of cancer patients. Given the relation between cancer incidence and age, this study examined the frequency of peripheral blood CD33(+)HLA-DR(−) MDSCs across three cohorts: healthy adults (19–59 years old), community-dwelling seniors (61–76 years old), and frail elderly (67–99 years old). This analysis is the first to demonstrate that MDSCs and specifically the CD11b(+)CD15(+) MDSC subset are increased with age. Proinflammatory cytokines that are required for the differentiation of MDSCs (e.g., TNF-α, IL-6, and IL-1β) were similarly found to be increased in the serum of the frail elderly. Furthermore, the proportion of MDSCs and the CD11b(+)CD15(+) subset were found to be elevated significantly in elderly donors with a history of cancer. This age-related elevation in the frequency of MDSCs may contribute to the increased cancer incidence that occurs with age. Further investigation into the functional consequences of elevated MDSCs will provide valuable insight into the progression of age-related pathologies. |
format | Online Article Text |
id | pubmed-3701116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Society for Leukocyte Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-37011162013-07-16 Blood CD33(+)HLA-DR(−) myeloid-derived suppressor cells are increased with age and a history of cancer Verschoor, Chris P. Johnstone, Jennie Millar, Jamie Dorrington, Michael G. Habibagahi, Mojtaba Lelic, Alina Loeb, Mark Bramson, Jonathan L. Bowdish, Dawn M. E. J Leukoc Biol Translational & Clinical Immunology As we age, the composition of our peripheral leukocytes changes dramatically. Many of these alterations contribute to the general immune dysfunction that burdens the elderly, which in turn, contributes to increased susceptibility to disease. MDSCs represent a heterogeneous population of immunosuppressive leukocytes that are elevated in the peripheral blood of cancer patients. Given the relation between cancer incidence and age, this study examined the frequency of peripheral blood CD33(+)HLA-DR(−) MDSCs across three cohorts: healthy adults (19–59 years old), community-dwelling seniors (61–76 years old), and frail elderly (67–99 years old). This analysis is the first to demonstrate that MDSCs and specifically the CD11b(+)CD15(+) MDSC subset are increased with age. Proinflammatory cytokines that are required for the differentiation of MDSCs (e.g., TNF-α, IL-6, and IL-1β) were similarly found to be increased in the serum of the frail elderly. Furthermore, the proportion of MDSCs and the CD11b(+)CD15(+) subset were found to be elevated significantly in elderly donors with a history of cancer. This age-related elevation in the frequency of MDSCs may contribute to the increased cancer incidence that occurs with age. Further investigation into the functional consequences of elevated MDSCs will provide valuable insight into the progression of age-related pathologies. Society for Leukocyte Biology 2013-04 /pmc/articles/PMC3701116/ /pubmed/23341539 http://dx.doi.org/10.1189/jlb.0912461 Text en © 2013 Society for Leukocyte Biology This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/us/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Translational & Clinical Immunology Verschoor, Chris P. Johnstone, Jennie Millar, Jamie Dorrington, Michael G. Habibagahi, Mojtaba Lelic, Alina Loeb, Mark Bramson, Jonathan L. Bowdish, Dawn M. E. Blood CD33(+)HLA-DR(−) myeloid-derived suppressor cells are increased with age and a history of cancer |
title | Blood CD33(+)HLA-DR(−) myeloid-derived suppressor cells are increased with age and a history of cancer |
title_full | Blood CD33(+)HLA-DR(−) myeloid-derived suppressor cells are increased with age and a history of cancer |
title_fullStr | Blood CD33(+)HLA-DR(−) myeloid-derived suppressor cells are increased with age and a history of cancer |
title_full_unstemmed | Blood CD33(+)HLA-DR(−) myeloid-derived suppressor cells are increased with age and a history of cancer |
title_short | Blood CD33(+)HLA-DR(−) myeloid-derived suppressor cells are increased with age and a history of cancer |
title_sort | blood cd33(+)hla-dr(−) myeloid-derived suppressor cells are increased with age and a history of cancer |
topic | Translational & Clinical Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3701116/ https://www.ncbi.nlm.nih.gov/pubmed/23341539 http://dx.doi.org/10.1189/jlb.0912461 |
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