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Bet-hedging in innate and adaptive immune systems

Immune system evolution is shaped by the fitness costs and trade-offs associated with mounting an immune response. Costs that arise mainly as a function of the magnitude of investment, including energetic and immunopathological costs, are well-represented in studies of immune system evolution. Less...

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Autores principales: Tate, Ann T, Van Cleve, Jeremy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9195227/
https://www.ncbi.nlm.nih.gov/pubmed/35712085
http://dx.doi.org/10.1093/emph/eoac021
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author Tate, Ann T
Van Cleve, Jeremy
author_facet Tate, Ann T
Van Cleve, Jeremy
author_sort Tate, Ann T
collection PubMed
description Immune system evolution is shaped by the fitness costs and trade-offs associated with mounting an immune response. Costs that arise mainly as a function of the magnitude of investment, including energetic and immunopathological costs, are well-represented in studies of immune system evolution. Less well considered, however, are the costs of immune cell plasticity and specialization. Hosts in nature encounter a large diversity of microbes and parasites that require different and sometimes conflicting immune mechanisms for defense, but it takes precious time to recognize and correctly integrate signals for an effective polarized response. In this perspective, we propose that bet-hedging can be a viable alternative to plasticity in immune cell effector function, discuss conditions under which bet-hedging is likely to be an advantageous strategy for different arms of the immune system, and present cases from both innate and adaptive immune systems that suggest bet-hedging at play.
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spelling pubmed-91952272022-06-15 Bet-hedging in innate and adaptive immune systems Tate, Ann T Van Cleve, Jeremy Evol Med Public Health Commentary Immune system evolution is shaped by the fitness costs and trade-offs associated with mounting an immune response. Costs that arise mainly as a function of the magnitude of investment, including energetic and immunopathological costs, are well-represented in studies of immune system evolution. Less well considered, however, are the costs of immune cell plasticity and specialization. Hosts in nature encounter a large diversity of microbes and parasites that require different and sometimes conflicting immune mechanisms for defense, but it takes precious time to recognize and correctly integrate signals for an effective polarized response. In this perspective, we propose that bet-hedging can be a viable alternative to plasticity in immune cell effector function, discuss conditions under which bet-hedging is likely to be an advantageous strategy for different arms of the immune system, and present cases from both innate and adaptive immune systems that suggest bet-hedging at play. Oxford University Press 2022-05-24 /pmc/articles/PMC9195227/ /pubmed/35712085 http://dx.doi.org/10.1093/emph/eoac021 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Foundation for Evolution, Medicine, and Public Health. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Tate, Ann T
Van Cleve, Jeremy
Bet-hedging in innate and adaptive immune systems
title Bet-hedging in innate and adaptive immune systems
title_full Bet-hedging in innate and adaptive immune systems
title_fullStr Bet-hedging in innate and adaptive immune systems
title_full_unstemmed Bet-hedging in innate and adaptive immune systems
title_short Bet-hedging in innate and adaptive immune systems
title_sort bet-hedging in innate and adaptive immune systems
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9195227/
https://www.ncbi.nlm.nih.gov/pubmed/35712085
http://dx.doi.org/10.1093/emph/eoac021
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