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Adverse environmental conditions influence age-related innate immune responsiveness
BACKGROUND-: The innate immune system plays an important role in the recognition and induction of protective responses against infectious pathogens, whilst there is increasing evidence for a role in mediating chronic inflammatory diseases at older age. Despite indications that environmental conditio...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2697140/ https://www.ncbi.nlm.nih.gov/pubmed/19480711 http://dx.doi.org/10.1186/1742-4933-6-7 |
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author | May, Linda van den Biggelaar, Anita HJ van Bodegom, David Meij, Hans J de Craen, Anton JM Amankwa, Joseph Frölich, Marijke Kuningas, Maris Westendorp, Rudi GJ |
author_facet | May, Linda van den Biggelaar, Anita HJ van Bodegom, David Meij, Hans J de Craen, Anton JM Amankwa, Joseph Frölich, Marijke Kuningas, Maris Westendorp, Rudi GJ |
author_sort | May, Linda |
collection | PubMed |
description | BACKGROUND-: The innate immune system plays an important role in the recognition and induction of protective responses against infectious pathogens, whilst there is increasing evidence for a role in mediating chronic inflammatory diseases at older age. Despite indications that environmental conditions can influence the senescence process of the adaptive immune system, it is not known whether the same holds true for the innate immune system. Therefore we studied whether age-related innate immune responses are similar or differ between populations living under very diverse environmental conditions. METHODS-: We compared cross-sectional age-related changes in ex vivo innate cytokine responses in a population living under affluent conditions in the Netherlands (age 20–68 years old, n = 304) and a population living under adverse environmental conditions in Ghana (age 23–95 years old, n = 562). RESULTS-: We found a significant decrease in LPS-induced Interleukin (IL)-10 and Tumor Necrosis Factor (TNF) production with age in the Dutch population. In Ghana a similar age-related decline in IL-10 responses to LPS, as well as to zymosan, or LPS plus zymosan, was observed. TNF production, however, did not show an age-associated decline, but increased significantly with age in response to co-stimulation with LPS and zymosan. CONCLUSION-: We conclude that the decline in innate cytokine responses is an intrinsic ageing phenomenon, while pathogen exposure and/or selective survival drive pro-inflammatory responses under adverse living conditions. |
format | Text |
id | pubmed-2697140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26971402009-06-16 Adverse environmental conditions influence age-related innate immune responsiveness May, Linda van den Biggelaar, Anita HJ van Bodegom, David Meij, Hans J de Craen, Anton JM Amankwa, Joseph Frölich, Marijke Kuningas, Maris Westendorp, Rudi GJ Immun Ageing Research BACKGROUND-: The innate immune system plays an important role in the recognition and induction of protective responses against infectious pathogens, whilst there is increasing evidence for a role in mediating chronic inflammatory diseases at older age. Despite indications that environmental conditions can influence the senescence process of the adaptive immune system, it is not known whether the same holds true for the innate immune system. Therefore we studied whether age-related innate immune responses are similar or differ between populations living under very diverse environmental conditions. METHODS-: We compared cross-sectional age-related changes in ex vivo innate cytokine responses in a population living under affluent conditions in the Netherlands (age 20–68 years old, n = 304) and a population living under adverse environmental conditions in Ghana (age 23–95 years old, n = 562). RESULTS-: We found a significant decrease in LPS-induced Interleukin (IL)-10 and Tumor Necrosis Factor (TNF) production with age in the Dutch population. In Ghana a similar age-related decline in IL-10 responses to LPS, as well as to zymosan, or LPS plus zymosan, was observed. TNF production, however, did not show an age-associated decline, but increased significantly with age in response to co-stimulation with LPS and zymosan. CONCLUSION-: We conclude that the decline in innate cytokine responses is an intrinsic ageing phenomenon, while pathogen exposure and/or selective survival drive pro-inflammatory responses under adverse living conditions. BioMed Central 2009-05-30 /pmc/articles/PMC2697140/ /pubmed/19480711 http://dx.doi.org/10.1186/1742-4933-6-7 Text en Copyright © 2009 May et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research May, Linda van den Biggelaar, Anita HJ van Bodegom, David Meij, Hans J de Craen, Anton JM Amankwa, Joseph Frölich, Marijke Kuningas, Maris Westendorp, Rudi GJ Adverse environmental conditions influence age-related innate immune responsiveness |
title | Adverse environmental conditions influence age-related innate immune responsiveness |
title_full | Adverse environmental conditions influence age-related innate immune responsiveness |
title_fullStr | Adverse environmental conditions influence age-related innate immune responsiveness |
title_full_unstemmed | Adverse environmental conditions influence age-related innate immune responsiveness |
title_short | Adverse environmental conditions influence age-related innate immune responsiveness |
title_sort | adverse environmental conditions influence age-related innate immune responsiveness |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2697140/ https://www.ncbi.nlm.nih.gov/pubmed/19480711 http://dx.doi.org/10.1186/1742-4933-6-7 |
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