Evidence map›Paper›PMID 28282024›Full record

ArticleeLife2017

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

Graeme Gossel, Thea Hogan, Daniel Cownden, Benedict Seddon, Andrew J Yates

Abstract read
In one paragraph

Article in eLife, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

58 citing papers in PubMed.

  1. Article
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  12. A variational deep-learning approach to modeling memory T cell dynamics.bioRxiv : the preprint server for biology · 2025
    Article
  13. Engineering memory T cells as a platform for long-term enzyme replacement therapy in lysosomal storage disorders.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  14. IL-7Rα on CD4Journal of neuroinflammation · 2024
    Article
  15. Article
  16. The dynamics and longevity of circulating CD4bioRxiv : the preprint server for biology · 2024
    Article
  17. Article
  18. Differentiation marker-negative CD4bioRxiv : the preprint server for biology · 2024
    Article
  19. Article
  20. KIR-HLA interactions extend human CD8+ T cell lifespan in vivo.The Journal of clinical investigation · 2023
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Graeme Gossel *Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary & Life Sciences University of Glasgow, Glasgow, United Kingdom.
Thea Hogan *Institute of Immunity and Transplantation, University College London, London, United Kingdom.
Daniel CowndenInstitute of Infection, Immunity and Inflammation, College of Medical, Veterinary & Life Sciences University of Glasgow, Glasgow, United Kingdom.
Benedict Seddon *Institute of Immunity and Transplantation, University College London, London, United Kingdom.
Andrew J Yates *Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary & Life Sciences University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0003-4606-4483

Funding

Modeling the development, structure and regulation of T cell memoryR01AI093870 · NIAID · UNIVERSITY OF GLASGOW · PI YATES, ANDREW · 2011 to 2025
$5.9M
Arthritis Research UKMedical Research Council MC-PC-13055NIAID NIH HHS R01 AI093870
6 · The paper itself

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.

Indexed as

Immunologic MemoryAnimalsCD4-Positive T-LymphocytesMiceT-Lymphocyte SubsetsBrdU labellingcomputational biologyimmunologyKi67mathematical modellingmemory T cellsmousesystems biologyT cell homeostasis

Identifiers

PMID28282024
PMCPMC5426903

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.