Human TSCM cell dynamics in vivo are compatible with long-lived immunological memory and stemness

• Published in: PLoS biology Vol. 16; no. 6; p. e2005523
• Main Authors: Costa del Amo, Pedro, Lahoz-Beneytez, Julio, Boelen, Lies, Ahmed, Raya, Miners, Kelly L., Zhang, Yan, Roger, Laureline, Jones, Rhiannon E., Marraco, Silvia A. Fuertes, Speiser, Daniel E., Baird, Duncan M., Price, David A., Ladell, Kristin, Macallan, Derek, Asquith, Becca
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 01.06.2018; Public Library of Science (PLoS)
• Subjects: Adaptive immunity; Adult; Aged, 80 and over; Antigens; Biochemistry, Molecular Biology; Biology and life sciences; Cancer; CD4-Positive T-Lymphocytes - cytology; CD4-Positive T-Lymphocytes - immunology; CD8-Positive T-Lymphocytes - cytology; CD8-Positive T-Lymphocytes - immunology; Cell Self Renewal - immunology; Cell self-renewal; Cellular Biology; Compatibility; Data processing; Dynamics; Funding; Genetics; Half-life; Human genetics; Humans; Immunity; Immunologic Memory; Immunological memory; Immunology; In vivo methods and tests; Infections; Kinetics; Labeling; Labelling; Life Sciences; Longevity; Lymphocytes; Lymphocytes T; Mathematical Concepts; Mathematical models; Medicine; Medicine and health sciences; Memory cells; Middle Aged; Models, Immunological; Population; Research and Analysis Methods; Software; Stable isotopes; Stem cells; Stochasticity; Subpopulations; Supervision; T cell receptors; T-Lymphocyte Subsets - cytology; T-Lymphocyte Subsets - immunology; Telomere Homeostasis - immunology; Yellow fever virus - immunology; New York; United Kingdom > UK; United States > US; Switzerland
• ISSN: 1545-7885; 1544-9173; 1545-7885
• DOI: 10.1371/journal.pbio.2005523

Adaptive immunity relies on the generation and maintenance of memory T cells to provide protection against repeated antigen exposure. It has been hypothesised that a self-renewing population of T cells, named stem cell-like memory T (TSCM) cells, are responsible for maintaining memory. However, it is not clear if the dynamics of TSCM cells in vivo are compatible with this hypothesis. To address this issue, we investigated the dynamics of TSCM cells under physiological conditions in humans in vivo using a multidisciplinary approach that combines mathematical modelling, stable isotope labelling, telomere length analysis, and cross-sectional data from vaccine recipients. We show that, unexpectedly, the average longevity of a TSCM clone is very short (half-life < 1 year, degree of self-renewal = 430 days): far too short to constitute a stem cell population. However, we also find that the TSCM population is comprised of at least 2 kinetically distinct subpopulations that turn over at different rates. Whilst one subpopulation is rapidly replaced (half-life = 5 months) and explains the rapid average turnover of the bulk TSCM population, the half-life of the other TSCM subpopulation is approximately 9 years, consistent with the longevity of the recall response. We also show that this latter population exhibited a high degree of self-renewal, with a cell residing without dying or differentiating for 15% of our lifetime. Finally, although small, the population was not subject to excessive stochasticity. We conclude that the majority of TSCM cells are not stem cell-like but that there is a subpopulation of TSCM cells whose dynamics are compatible with their putative role in the maintenance of T cell memory.