Evidence map›Paper›PMID 24927527›Full record

Trial reportProceedings of the National Academy of Sciences of the United States of America2014

Human memory T cells from the bone marrow are resting and maintain long-lasting systemic memory.

Anna Okhrimenko, Joachim R Grün, Kerstin Westendorf, Zhuo Fang, Simon Reinke, Philipp von Roth, Georgi Wassilew, Anja A Kühl, Robert Kudernatsch, Sonya Demski and 9 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 125 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
125citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% of its field
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

125 citing papers in PubMed, 1 synthesis or guideline pooled it, 182 citations in OpenAlex.

  1. Tissue-Resident Memory T Cells in Skin Diseases: A Systematic Review.International journal of molecular sciences · 2021
    Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. PD-1 Inhibits CD4+ TRM-Mediated cDC1 Mobilization via Suppressing JAML in Human NSCLC.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  7. Review
  8. Review
  9. Article
  10. Article
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  15. Article
  16. Tumor-specific CD8Journal for immunotherapy of cancer · 2025
    Article
  17. Review
  18. Article
  19. Article
  20. Article

65 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 4 institutions in 2 countries.

Anna OkhrimenkoCell Biology.
Joachim R GrünBioinformatics.
Kerstin WestendorfCell Biology.
Zhuo FangCell Biology,Signal Transduction, and.
Simon ReinkeCore Unit Cell Harvesting, Berlin-Brandenburg Center for Regenerative Therapies and.
Philipp von RothCenter for Musculoskeletal Surgery and.
Georgi WassilewCenter for Musculoskeletal Surgery and.
Anja A KühlDepartment of Gastroenterology, Infectiology and Rheumatology, Charité University of Medicine Berlin, 12200 Berlin, Germany.
Robert KudernatschClinical Tumor Immunology and Immunemonitoring, Institute for Medical Immunology, Charité University of Medicine Berlin, 13353 Berlin, Germany;
Sonya DemskiClinical Tumor Immunology and Immunemonitoring, Institute for Medical Immunology, Charité University of Medicine Berlin, 13353 Berlin, Germany;
Carmen ScheibenbogenClinical Tumor Immunology and Immunemonitoring, Institute for Medical Immunology, Charité University of Medicine Berlin, 13353 Berlin, Germany;
Koji TokoyodaOsteoimmunology, Deutsches Rheuma-Forschungszentrum Berlin, 10117 Berlin, Germany;
Mairi A McGrathCell Biology.
Martin J RafteryInstitute of Virology, Charité University of Medicine Berlin, 10117 Berlin, Germany; and.
Günther SchönrichInstitute of Virology, Charité University of Medicine Berlin, 10117 Berlin, Germany; and.
Alessandro SerraCell Biology.
Hyun-Dong ChangCell Biology.
Andreas RadbruchCell Biology.
Jun DongCell Biology, dong@drfz.de.
Charité - Universitätsmedizin Berlin · DEInstitute for Musculoskeletal Health · AUBerlin-Brandenburger Centrum für Regenerative Therapien · DEGerman Rheumatism Research Centre · DE

Funding

European Research Council 268987
6 · The paper itself

Abstract

In the bone marrow, a population of memory T cells has been described that promotes efficient secondary immune responses and has been considered to be preactivated, owing to its expression of CD69 and CD25. Here we show that human bone marrow professional memory T cells are not activated but are resting in terms of proliferation, transcription, and mobility. They are in the G0 phase of the cell cycle, and their transcriptome is that of resting T cells. The repertoire of CD4(+) bone marrow memory T cells compared with CD4(+) memory T cells from the blood is significantly enriched for T cells specific for cytomegalovirus-pp65 (immunodominant protein), tetanus toxoid, measles, mumps, and rubella. It is not enriched for vaccinia virus and Candida albicans-MP65 (immunodominant protein), typical pathogens of skin and/or mucosa. CD4(+) memory T cells specific for measles are maintained nearly exclusively in the bone marrow. Thus, CD4(+) memory T cells from the bone marrow provide long-term memory for systemic pathogens.

Indexed as

AdultAntigens, CDAntigens, Differentiation, T-LymphocyteBone Marrow CellsCD4-Positive T-LymphocytesCD69 AntigensFemaleHumansImmunologic MemoryInterleukin-2 Receptor alpha SubunitLectins, C-TypeMaleMiddle AgedResting Phase, Cell CycleAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensIL2RA protein, humanInterleukin-2 Receptor alpha SubunitLectins, C-Typeantigen-specific responsepolyfunctionalshort- and long-term memory

Identifiers

PMID24927527
PMCPMC4078840
OpenAlexW2144463184

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.