Journal article

Early priming minimizes the age-related immune compromise of CD8 T cell diversity and function

SA Valkenburg, V Venturi, THY Dang, NL Bird, PC Doherty, SJ Turner, MP Davenport, K Kedzierska

Plos Pathogens | Published : 2012

Abstract

The elderly are particularly susceptible to influenza A virus infections, with increased occurrence, disease severity and reduced vaccine efficacy attributed to declining immunity. Experimentally, the age-dependent decline in influenza-specific CD8+ T cell responsiveness reflects both functional compromise and the emergence of 'repertoire holes' arising from the loss of low frequency clonotypes. In this study, we asked whether early priming limits the time-related attrition of immune competence. Though primary responses in aged mice were compromised, animals vaccinated at 6 weeks then challenged >20 months later had T-cell responses that were normal in magnitude. Both functional quality and ..

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Grants

Awarded by Australian Research Council


Funding Acknowledgements

This work was supported by Australian National Health and Medical Research Council (NHMRC) Project Grants to KK (AI454312; AI1008854), an NHMRC Program Grant (APP567122) to PCD and SJT, an ARC Project Grant to MPD, SJT, and VV (DP0771340) and NIH grant (AI170251) to PCD. SAV is a recipient of the Australian Postgraduate Award, KK is an NHMRC RD Wright Fellow, SJT is a Pfizer Australia Senior Research Fellow, VV is an ARC Future Fellow and MPD is an NHMRC Senior Research Fellow. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.