Aging-induced fragility of the immune system. (7th February 2021)

• Record Type: Journal Article
• Authors: Jones, Eric; Sheng, Jiming; Carlson, Jean; Wang, Shenshen
• Is Part Of: Journal of theoretical biology. Volume 510(2021)
• Publication Date: 2021-02-07
• Subjects: Immunosenescence -- Innate and adaptive immune responses -- Computational and systems biology -- Mathematical modeling; Biology -- Periodicals; Biological Science Disciplines -- Periodicals; Biology -- Periodicals; Biologie -- Périodiques; Theoretische biologie; Biology; Periodicals; 571.05
• DOI: 10.1016/j.jtbi.2020.110473
• Languages: English
• ISSNs: 0022-5193

Abstract

Highlights: Innate-adaptive immune collaboration deteriorates with age, resulting in fragility. Imbalance of the adaptive repertoire triggers chronic inflammation in the elderly. Variability in the onset of fragility arises from individual infection histories. Trade-off exists between pathogen clearance and inflammation suppression. Abstract: 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.