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Nature Reviews Immunology
Article . 2013 . Peer-reviewed
License: Springer TDM
Data sources: Crossref
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Age-dependent dysregulation of innate immunity

Authors: Albert C, Shaw; Daniel R, Goldstein; Ruth R, Montgomery;

Age-dependent dysregulation of innate immunity

Abstract

As we age, the innate immune system becomes dysregulated and is characterized by persistent inflammatory responses that involve multiple immune and non-immune cell types and that vary depending on the cell activation state and tissue context. This ageing-associated basal inflammation, particularly in humans, is thought to be induced by several factors, including the reactivation of latent viral infections and the release of endogenous damage-associated ligands of pattern recognition receptors (PRRs). Innate immune cell functions that are required to respond to pathogens or vaccines, such as cell migration and PRR signalling, are also impaired in aged individuals. This immune dysregulation may affect conditions associated with chronic inflammation, such as atherosclerosis and Alzheimer's disease.

Related Organizations
Keywords

Inflammation, Aging, Immunity, Cellular, Mice, Receptors, Pattern Recognition, Age Factors, Animals, Humans, Immunity, Innate

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
922
Top 0.1%
Top 0.1%
Top 0.1%
bronze