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Plasmacytoid dendritic cell and myeloid dendritic cell function in ageing: A comparison between elderly and young adult women
Ageing is associated with a changing immune system, leading to inflammageing (increased levels of inflammation markers in serum) and immunosenescence (reduced immune cells and reduced responses towards pathogens). This results in reduced vaccination responses and increased infections in elderly. Muc...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6907850/ https://www.ncbi.nlm.nih.gov/pubmed/31830086 http://dx.doi.org/10.1371/journal.pone.0225825 |
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author | van Splunter, Marloes Perdijk, Olaf Fick-Brinkhof, Henriëtte Floris-Vollenbroek, Esther G. Meijer, Ben Brugman, Sylvia Savelkoul, Huub F. J. van Hoffen, Els Joost van Neerven, R. J. |
author_facet | van Splunter, Marloes Perdijk, Olaf Fick-Brinkhof, Henriëtte Floris-Vollenbroek, Esther G. Meijer, Ben Brugman, Sylvia Savelkoul, Huub F. J. van Hoffen, Els Joost van Neerven, R. J. |
author_sort | van Splunter, Marloes |
collection | PubMed |
description | Ageing is associated with a changing immune system, leading to inflammageing (increased levels of inflammation markers in serum) and immunosenescence (reduced immune cells and reduced responses towards pathogens). This results in reduced vaccination responses and increased infections in elderly. Much is known about the adaptive immune system upon ageing, but less is known about the innate immune system. Therefore, the aim of this study was to compare innate immune function of Toll like receptor (TLR)-mediated responses between elderly and young adult women. To this end, elderly and young adult women were compared to study the effect of ageing on the relative prevalence and reactivity to TLR-mediated responses of myeloid- and plasmacytoid dendritic cells (mDC, pDC). In addition, TLR expression and inflammatory markers in serum were investigated. Elderly women had reduced numbers of circulating pDCs. In addition, pDCs and mDCs of elderly women responded differently towards TLR stimulation, especially TLR7/8 mediated stimulation was reduced, compared to young adults. In serum, markers involved in inflammation were generally increased in elderly. In conclusion, this study confirms and extends the knowledge about immunosenescence and inflammageing on innate immunity in elderly women. |
format | Online Article Text |
id | pubmed-6907850 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-69078502019-12-27 Plasmacytoid dendritic cell and myeloid dendritic cell function in ageing: A comparison between elderly and young adult women van Splunter, Marloes Perdijk, Olaf Fick-Brinkhof, Henriëtte Floris-Vollenbroek, Esther G. Meijer, Ben Brugman, Sylvia Savelkoul, Huub F. J. van Hoffen, Els Joost van Neerven, R. J. PLoS One Research Article Ageing is associated with a changing immune system, leading to inflammageing (increased levels of inflammation markers in serum) and immunosenescence (reduced immune cells and reduced responses towards pathogens). This results in reduced vaccination responses and increased infections in elderly. Much is known about the adaptive immune system upon ageing, but less is known about the innate immune system. Therefore, the aim of this study was to compare innate immune function of Toll like receptor (TLR)-mediated responses between elderly and young adult women. To this end, elderly and young adult women were compared to study the effect of ageing on the relative prevalence and reactivity to TLR-mediated responses of myeloid- and plasmacytoid dendritic cells (mDC, pDC). In addition, TLR expression and inflammatory markers in serum were investigated. Elderly women had reduced numbers of circulating pDCs. In addition, pDCs and mDCs of elderly women responded differently towards TLR stimulation, especially TLR7/8 mediated stimulation was reduced, compared to young adults. In serum, markers involved in inflammation were generally increased in elderly. In conclusion, this study confirms and extends the knowledge about immunosenescence and inflammageing on innate immunity in elderly women. Public Library of Science 2019-12-12 /pmc/articles/PMC6907850/ /pubmed/31830086 http://dx.doi.org/10.1371/journal.pone.0225825 Text en © 2019 Splunter et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article van Splunter, Marloes Perdijk, Olaf Fick-Brinkhof, Henriëtte Floris-Vollenbroek, Esther G. Meijer, Ben Brugman, Sylvia Savelkoul, Huub F. J. van Hoffen, Els Joost van Neerven, R. J. Plasmacytoid dendritic cell and myeloid dendritic cell function in ageing: A comparison between elderly and young adult women |
title | Plasmacytoid dendritic cell and myeloid dendritic cell function in ageing: A comparison between elderly and young adult women |
title_full | Plasmacytoid dendritic cell and myeloid dendritic cell function in ageing: A comparison between elderly and young adult women |
title_fullStr | Plasmacytoid dendritic cell and myeloid dendritic cell function in ageing: A comparison between elderly and young adult women |
title_full_unstemmed | Plasmacytoid dendritic cell and myeloid dendritic cell function in ageing: A comparison between elderly and young adult women |
title_short | Plasmacytoid dendritic cell and myeloid dendritic cell function in ageing: A comparison between elderly and young adult women |
title_sort | plasmacytoid dendritic cell and myeloid dendritic cell function in ageing: a comparison between elderly and young adult women |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6907850/ https://www.ncbi.nlm.nih.gov/pubmed/31830086 http://dx.doi.org/10.1371/journal.pone.0225825 |
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