Cargando…
Cellular senescence is a key mediator of lung aging and susceptibility to infection
Aging results in systemic changes that leave older adults at much higher risk for adverse outcomes following respiratory infections. Much work has been done over the years to characterize and describe the varied changes that occur with aging from the molecular/cellular up to the organismal level. In...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9473698/ https://www.ncbi.nlm.nih.gov/pubmed/36119079 http://dx.doi.org/10.3389/fimmu.2022.1006710 |
_version_ | 1784789558998597632 |
---|---|
author | Torrance, Blake L. Haynes, Laura |
author_facet | Torrance, Blake L. Haynes, Laura |
author_sort | Torrance, Blake L. |
collection | PubMed |
description | Aging results in systemic changes that leave older adults at much higher risk for adverse outcomes following respiratory infections. Much work has been done over the years to characterize and describe the varied changes that occur with aging from the molecular/cellular up to the organismal level. In recent years, the systemic accumulation of senescent cells has emerged as a key mediator of many age-related declines and diseases of aging. Many of these age-related changes can impair the normal function of the respiratory system and its capability to respond appropriately to potential pathogens that are encountered daily. In this review, we aim to establish the effects of cellular senescence on the disruption of normal lung function with aging and describe how these effects compound to leave an aged respiratory system at great risk when exposed to a pathogen. We will also discuss the role cellular senescence may play in the inability of most vaccines to confer protection against respiratory infections when administered to older adults. We posit that cellular senescence may be the point of convergence of many age-related immunological declines. Enhanced investigation into this area could provide much needed insight to understand the aging immune system and how to effectively ameliorate responses to pathogens that continue to disproportionately harm this vulnerable population. |
format | Online Article Text |
id | pubmed-9473698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94736982022-09-15 Cellular senescence is a key mediator of lung aging and susceptibility to infection Torrance, Blake L. Haynes, Laura Front Immunol Immunology Aging results in systemic changes that leave older adults at much higher risk for adverse outcomes following respiratory infections. Much work has been done over the years to characterize and describe the varied changes that occur with aging from the molecular/cellular up to the organismal level. In recent years, the systemic accumulation of senescent cells has emerged as a key mediator of many age-related declines and diseases of aging. Many of these age-related changes can impair the normal function of the respiratory system and its capability to respond appropriately to potential pathogens that are encountered daily. In this review, we aim to establish the effects of cellular senescence on the disruption of normal lung function with aging and describe how these effects compound to leave an aged respiratory system at great risk when exposed to a pathogen. We will also discuss the role cellular senescence may play in the inability of most vaccines to confer protection against respiratory infections when administered to older adults. We posit that cellular senescence may be the point of convergence of many age-related immunological declines. Enhanced investigation into this area could provide much needed insight to understand the aging immune system and how to effectively ameliorate responses to pathogens that continue to disproportionately harm this vulnerable population. Frontiers Media S.A. 2022-08-31 /pmc/articles/PMC9473698/ /pubmed/36119079 http://dx.doi.org/10.3389/fimmu.2022.1006710 Text en Copyright © 2022 Torrance and Haynes https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Torrance, Blake L. Haynes, Laura Cellular senescence is a key mediator of lung aging and susceptibility to infection |
title | Cellular senescence is a key mediator of lung aging and susceptibility to infection |
title_full | Cellular senescence is a key mediator of lung aging and susceptibility to infection |
title_fullStr | Cellular senescence is a key mediator of lung aging and susceptibility to infection |
title_full_unstemmed | Cellular senescence is a key mediator of lung aging and susceptibility to infection |
title_short | Cellular senescence is a key mediator of lung aging and susceptibility to infection |
title_sort | cellular senescence is a key mediator of lung aging and susceptibility to infection |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9473698/ https://www.ncbi.nlm.nih.gov/pubmed/36119079 http://dx.doi.org/10.3389/fimmu.2022.1006710 |
work_keys_str_mv | AT torranceblakel cellularsenescenceisakeymediatoroflungagingandsusceptibilitytoinfection AT hayneslaura cellularsenescenceisakeymediatoroflungagingandsusceptibilitytoinfection |