Memory CD4 T cell subsets are kinetically heterogeneous and replenished from naive T cells at high levels

Author:

Gossel Graeme12,Hogan Thea3,Cownden Daniel1,Seddon Benedict3,Yates Andrew J1ORCID

Affiliation:

1. Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary & Life Sciences University of Glasgow, Glasgow, United Kingdom

2. Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, United States

3. Institute of Immunity and Transplantation, University College London, London, United Kingdom

Abstract

Characterising the longevity of immunological memory requires establishing the rules underlying the renewal and death of peripheral T cells. However, we lack knowledge of the population structure and how self-renewal and de novo influx contribute to the maintenance of memory compartments. Here, we characterise the kinetics and structure of murine CD4 T cell memory subsets by measuring the rates of influx of new cells and using detailed timecourses of DNA labelling that also distinguish the behaviour of recently divided and quiescent cells. We find that both effector and central memory CD4 T cells comprise subpopulations with highly divergent rates of turnover, and show that inflows of new cells sourced from the naive pool strongly impact estimates of memory cell lifetimes and division rates. We also demonstrate that the maintenance of CD4 T cell memory subsets in healthy mice is unexpectedly and strikingly reliant on this replenishment.

Funder

National Institutes of Health

Arthritis Research UK

Medical Research Council

National Science Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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