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Study reveals how chronic inflammation drives age-associated CD8+ T cell remodeling

By

Gwendalyn J. Randolph1 Send email to [email protected]

4d ago· 64 min readenNews

Summary

This study by Shchukina et al. investigates how aging and chronic low-grade inflammation remodel the CD8+ T cell compartment. The researchers demonstrate that age-associated GZMK+CD8+ T cells (TAA cells) develop through a cell-extrinsic pathway requiring antigen exposure within aged non-lymphoid tissues. Using a TNFΔ69AU/+ mouse model, they show that low-grade inflammation accelerates CD8+ T cell aging and promotes early accumulation of TAA cells. The study further reveals that TAA cells are sustained by a progenitor population enriched in adipose tissue.

Key quotes

· 4 pulled
Aging strongly impacts CD8+ T cells, including the loss of naive cells and the emergence of age-associated GZMK+CD8+ T cells (TAA cells).
TAA cell development is cell extrinsic and requires antigen exposure within aged non-lymphoid tissues.
Low-grade inflammation accelerates CD8+ T cell aging and promotes early accumulation of TAA cells.
Age-associated GZMK+CD8+ T cells arise following antigen exposure in non-lymphoid tissues and are sustained by a progenitor population enriched in adipose tissue.
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In this study, Shchukina et al. show how aging and chronic low-grade inflammation remodel the CD8+ T cell compartment. Age-associated GZMK+CD8+ T cells arise following antigen exposure in non-lymphoid tissues and are sustained by a progenitor population e

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