4.5 Review

The life cycle of a T cell after vaccination - where does immune ageing strike?

Journal

CLINICAL AND EXPERIMENTAL IMMUNOLOGY
Volume 187, Issue 1, Pages 71-81

Publisher

OXFORD UNIV PRESS
DOI: 10.1111/cei.12829

Keywords

aging; immunosenescence; T cell memory; T cell receptor repertoire; T cell response

Categories

Funding

  1. National Institutes of Health [R01 AR042527, R01 AI044142, HL 117913, R01 AI108906, P01 HL058000, R01 AI108891, R01 AG045779, U19 AI057229, U19 AI057266, I01 BX001669]

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Vaccination is the optimal intervention to prevent the increased morbidity and mortality from infection in older individuals and to maintain immune health during ageing. To optimize benefits from vaccination, strategies have to be developed that overcome the defects in an adaptive immune response that occur with immune ageing. Most current approaches are concentrated on activating the innate immune system by adjuvants to improve the induction of a T cell response. This review will focus upon T cell-intrinsic mechanisms that control how a T cell is activated, expands rapidly to differentiate into short-lived effector cells and into memory precursor cells, with short-lived effector T cells then mainly undergoing apoptosis and memory precursor cells surviving as long-lived memory T cells. Insights into each step of this longitudinal course of a T cell response that takes place over a period of several weeks is beginning to allow identifying interventions that can improve this process of T cell memory generation and specifically target defects that occur with ageing.

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