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Rheumatoid Arthritis, Immunosenescence and the Hallmarks of Aging
Age is the most important risk factor for the development of infectious diseases, cancer and chronic inflammatory diseases including rheumatoid arthritis (RA). The very act of living causes damage to cells. A network of molecular, cellular and physiological maintenance and repair systems creates a b...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Science Publishers
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388800/ https://www.ncbi.nlm.nih.gov/pubmed/26212057 http://dx.doi.org/10.2174/1874609808666150727110744 |
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author | Chalan, Paulina van den Berg, Anke Kroesen, Bart-Jan Brouwer, Liesbeth Boots, Annemieke |
author_facet | Chalan, Paulina van den Berg, Anke Kroesen, Bart-Jan Brouwer, Liesbeth Boots, Annemieke |
author_sort | Chalan, Paulina |
collection | PubMed |
description | Age is the most important risk factor for the development of infectious diseases, cancer and chronic inflammatory diseases including rheumatoid arthritis (RA). The very act of living causes damage to cells. A network of molecular, cellular and physiological maintenance and repair systems creates a buffering capacity against these damages. Aging leads to progressive shrinkage of the buffering capacity and increases vulnerability. In order to better understand the complex mammalian aging processes, nine hallmarks of aging and their interrelatedness were recently put forward. RA is a chronic autoimmune disease affecting the joints. Although RA may develop at a young age, the incidence of RA increases with age. It has been suggested that RA may develop as a consequence of premature aging (immunosenescence) of the immune system. Alternatively, premature aging may be the consequence of the inflammatory state in RA. In an effort to answer this chicken and egg conundrum, we here outline and discuss the nine hallmarks of aging, their contribution to the pre-aged phenotype and the effects of treatment on the reversibility of immunosenescence in RA. |
format | Online Article Text |
id | pubmed-5388800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Bentham Science Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-53888002017-04-12 Rheumatoid Arthritis, Immunosenescence and the Hallmarks of Aging Chalan, Paulina van den Berg, Anke Kroesen, Bart-Jan Brouwer, Liesbeth Boots, Annemieke Curr Aging Sci Article Age is the most important risk factor for the development of infectious diseases, cancer and chronic inflammatory diseases including rheumatoid arthritis (RA). The very act of living causes damage to cells. A network of molecular, cellular and physiological maintenance and repair systems creates a buffering capacity against these damages. Aging leads to progressive shrinkage of the buffering capacity and increases vulnerability. In order to better understand the complex mammalian aging processes, nine hallmarks of aging and their interrelatedness were recently put forward. RA is a chronic autoimmune disease affecting the joints. Although RA may develop at a young age, the incidence of RA increases with age. It has been suggested that RA may develop as a consequence of premature aging (immunosenescence) of the immune system. Alternatively, premature aging may be the consequence of the inflammatory state in RA. In an effort to answer this chicken and egg conundrum, we here outline and discuss the nine hallmarks of aging, their contribution to the pre-aged phenotype and the effects of treatment on the reversibility of immunosenescence in RA. Bentham Science Publishers 2015-07 2015-07 /pmc/articles/PMC5388800/ /pubmed/26212057 http://dx.doi.org/10.2174/1874609808666150727110744 Text en © 2015 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Chalan, Paulina van den Berg, Anke Kroesen, Bart-Jan Brouwer, Liesbeth Boots, Annemieke Rheumatoid Arthritis, Immunosenescence and the Hallmarks of Aging |
title | Rheumatoid Arthritis, Immunosenescence and the Hallmarks of Aging |
title_full | Rheumatoid Arthritis, Immunosenescence and the Hallmarks of Aging |
title_fullStr | Rheumatoid Arthritis, Immunosenescence and the Hallmarks of Aging |
title_full_unstemmed | Rheumatoid Arthritis, Immunosenescence and the Hallmarks of Aging |
title_short | Rheumatoid Arthritis, Immunosenescence and the Hallmarks of Aging |
title_sort | rheumatoid arthritis, immunosenescence and the hallmarks of aging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388800/ https://www.ncbi.nlm.nih.gov/pubmed/26212057 http://dx.doi.org/10.2174/1874609808666150727110744 |
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