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Aging-induced fragility of the immune system
The adaptive and innate branches of the vertebrate immune system work in close collaboration to protect organisms from harmful pathogens. As an organism ages its immune system undergoes immunosenescence, characterized by declined performance or malfunction in either immune branch, which can lead to...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7487974/ https://www.ncbi.nlm.nih.gov/pubmed/32941914 http://dx.doi.org/10.1016/j.jtbi.2020.110473 |
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author | Jones, Eric Sheng, Jiming Carlson, Jean Wang, Shenshen |
author_facet | Jones, Eric Sheng, Jiming Carlson, Jean Wang, Shenshen |
author_sort | Jones, Eric |
collection | PubMed |
description | The adaptive and innate branches of the vertebrate immune system work in close collaboration to protect organisms from harmful pathogens. As an organism ages its immune system undergoes immunosenescence, characterized by declined performance or malfunction in either immune branch, which can lead to disease and death. In this study we develop a mathematical framework of coupled innate and adaptive immune responses, namely the integrated immune branch (IIB) model. This model describes dynamics of immune components in both branches, uses a shape-space representation to encode pathogen-specific immune memory, and exhibits three steady states – health, septic death, and chronic inflammation – qualitatively similar to clinically-observed immune outcomes. In this model, the immune system (initialized in the health state) is subjected to a sequence of pathogen encounters, and we use the number of prior pathogen encounters as a proxy for the “age” of the immune system. We find that repeated pathogen encounters may trigger a fragility in which any encounter with a novel pathogen will cause the system to irreversibly switch from health to chronic inflammation. This transition is consistent with the onset of “inflammaging”, a condition observed in aged individuals who experience chronic low-grade inflammation even in the absence of pathogens. The IIB model predicts that the onset of chronic inflammation strongly depends on the history of encountered pathogens; the timing of onset differs drastically when the same set of infections occurs in a different order. Lastly, the coupling between the innate and adaptive immune branches generates a trade-off between rapid pathogen clearance and a delayed onset of immunosenescence. Overall, by considering the complex feedback between immune compartments, our work suggests potential mechanisms for immunosenescence and provides a theoretical framework at the system level and on the scale of an organism’s lifetime to account for clinical observations. |
format | Online Article Text |
id | pubmed-7487974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74879742020-09-14 Aging-induced fragility of the immune system Jones, Eric Sheng, Jiming Carlson, Jean Wang, Shenshen J Theor Biol Article The adaptive and innate branches of the vertebrate immune system work in close collaboration to protect organisms from harmful pathogens. As an organism ages its immune system undergoes immunosenescence, characterized by declined performance or malfunction in either immune branch, which can lead to disease and death. In this study we develop a mathematical framework of coupled innate and adaptive immune responses, namely the integrated immune branch (IIB) model. This model describes dynamics of immune components in both branches, uses a shape-space representation to encode pathogen-specific immune memory, and exhibits three steady states – health, septic death, and chronic inflammation – qualitatively similar to clinically-observed immune outcomes. In this model, the immune system (initialized in the health state) is subjected to a sequence of pathogen encounters, and we use the number of prior pathogen encounters as a proxy for the “age” of the immune system. We find that repeated pathogen encounters may trigger a fragility in which any encounter with a novel pathogen will cause the system to irreversibly switch from health to chronic inflammation. This transition is consistent with the onset of “inflammaging”, a condition observed in aged individuals who experience chronic low-grade inflammation even in the absence of pathogens. The IIB model predicts that the onset of chronic inflammation strongly depends on the history of encountered pathogens; the timing of onset differs drastically when the same set of infections occurs in a different order. Lastly, the coupling between the innate and adaptive immune branches generates a trade-off between rapid pathogen clearance and a delayed onset of immunosenescence. Overall, by considering the complex feedback between immune compartments, our work suggests potential mechanisms for immunosenescence and provides a theoretical framework at the system level and on the scale of an organism’s lifetime to account for clinical observations. Elsevier Ltd. 2021-02-07 2020-09-14 /pmc/articles/PMC7487974/ /pubmed/32941914 http://dx.doi.org/10.1016/j.jtbi.2020.110473 Text en © 2020 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Jones, Eric Sheng, Jiming Carlson, Jean Wang, Shenshen Aging-induced fragility of the immune system |
title | Aging-induced fragility of the immune system |
title_full | Aging-induced fragility of the immune system |
title_fullStr | Aging-induced fragility of the immune system |
title_full_unstemmed | Aging-induced fragility of the immune system |
title_short | Aging-induced fragility of the immune system |
title_sort | aging-induced fragility of the immune system |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7487974/ https://www.ncbi.nlm.nih.gov/pubmed/32941914 http://dx.doi.org/10.1016/j.jtbi.2020.110473 |
work_keys_str_mv | AT joneseric aginginducedfragilityoftheimmunesystem AT shengjiming aginginducedfragilityoftheimmunesystem AT carlsonjean aginginducedfragilityoftheimmunesystem AT wangshenshen aginginducedfragilityoftheimmunesystem |