4.5 Article

Variations in immune parameters with age in a wild rodent population and links with survival

期刊

ECOLOGY AND EVOLUTION
卷 12, 期 7, 页码 -

出版社

WILEY
DOI: 10.1002/ece3.9094

关键词

aging; immune cells; immune remodeling; immunosenescence; mammal; Marmota marmota; survival

资金

  1. Agence Nationale de la Recherche [ANR-13-JSV7-0005]

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Recent findings suggest that immune functions can adaptively remodel with age, with some functions being downregulated while others are upregulated. Longitudinal studies are needed to understand the patterns and consequences of age variations in the immune system in wild populations. Changes in immune parameters with age could be due to within-individual variations and/or selective disappearance of individuals with peculiar immune phenotypes. A study on a wild Alpine marmot population reveals that the relative number of lymphocytes decreases and the relative number of neutrophils increases with age, and individuals with fewer lymphocytes and more neutrophils are more likely to die.
Recent findings suggest that immune functions do not unidirectionally deteriorate with age but that a potentially adaptive remodeling, where functions of the immune system get downregulated while others get upregulated with age could also occur. Scarce in wild populations, longitudinal studies are yet necessary to properly understand the patterns and consequences of age variations of the immune system in the wild. Meanwhile, it is challenging to understand if the observed variations in immune parameters with age are due to changes at the within-individual level or to selective (dis)appearance of individuals with peculiar immune phenotypes. Thanks to a long-term and longitudinal monitoring of a wild Alpine marmot population, we aimed to understand within- and between-individual variation in the immune phenotype with age, in order to improve our knowledge about the occurrence and the evolutionary consequences of such age variations in the wild. To do so, we recorded the age-specific leukocyte concentration and leukocyte profile in repeatedly sampled dominant individuals. We then tested whether the potential changes with age were attributable to within-individual variations and/or selective (dis)appearance. Finally, we investigated if the leukocyte concentration and profiles were correlated to the probability of death at a given age. The leukocyte concentration was stable with age, but the relative number of lymphocytes decreased, while the relative number of neutrophils increased, over the course of an individual's life. Moreover, between individuals of the same age, individuals with fewer lymphocytes but more neutrophils were more likely to die. Therefore, selective disappearance seems to play a role in the age variations of the immune parameters in this population. Further investigations linking age variations in immune phenotype to individual fitness are needed to understand whether remodeling of the immune system with age could or could not be adaptive.

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