Logo image
Enhancement of virus-specific expansion of transgenic CD8 T cells in aged mice by dendritic cells
Journal article   Open access   Peer reviewed

Enhancement of virus-specific expansion of transgenic CD8 T cells in aged mice by dendritic cells

Jiu Jiang, Erin Fisher, Andrew J Bennett and Donna M Murasko
Mechanisms of ageing and development, v 131(9), pp 580-583
2010
PMID: 20728463
url
https://doi.org/10.1016/j.mad.2010.08.003View
Published, Version of Record (VoR) Open

Abstract

Aging Dendritic cells T cells Viral
▶ The role of dendritic cells (DCs) in the age-associated decrease was examined. ▶ Influenza-specific TCR transgenic CD8 T cells of young mice demonstrated limited expansion in response to influenza infection when adoptively transferred to aged compared to young mice. ▶ This decreased response in aged mice could be significantly enhanced when DCs of young mice were co-transferred. Co-transfer of DCs had no impact in young recipient mice. ▶ These results suggest that the diminished CD8 T cell response to virus infection in aged mice is partially attributable to age-associated changes in DCs. Aging is associated with a decreased CD8 T cell response to multiple antigens and to virus infection. Although both intrinsic and extrinsic factors have been shown to contribute to the decrease, the mechanisms are still largely unknown. In this study, the role of dendritic cells (DCs) in the age-associated decrease was examined. Influenza-specific TCR transgenic CD8 T cells of young mice demonstrated limited expansion in response to influenza infection when adoptively transferred to aged compared to young mice. This decreased response in aged mice could be significantly enhanced when DCs of young mice were co-transferred. Co-transfer of DCs had no impact in young recipient mice. Adoptive transfer of the DCs also increased the endogenous CD8 T cell response of intact aged mice, although to a lesser degree. These results suggest that the diminished CD8 T cell response to virus infection in aged mice is partially attributable to age-associated changes in DCs.

Metrics

3 Record Views
12 citations in Scopus

Details

UN Sustainable Development Goals (SDGs)

This publication has contributed to the advancement of the following goals:

#3 Good Health and Well-Being

InCites Highlights

Data related to this publication, from InCites Benchmarking & Analytics tool:

Web of Science research areas
Cell Biology
Geriatrics & Gerontology
Logo image