Evidence map›Paper›PMID 27129922›Full record

ArticleEuropean journal of immunology2016

Distinct IL-7 signaling in recent thymic emigrants versus mature naïve T cells controls T-cell homeostasis.

Hye Kyung Kim, Adam T Waickman, Ehydel Castro, Francis A Flomerfelt, Nga V Hawk, Veena Kapoor, William G Telford, Ronald E Gress

Open access · greenAbstract read
In one paragraph

Article in European journal of immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Advances in IL-7 Research on Tumour Therapy.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  5. Sex-specific differences in ICOSClinical and experimental medicine · 2024
    Article
  6. The Role of IL-7 and IL-7R in Cancer Pathophysiology and Immunotherapy.International journal of molecular sciences · 2022
    Review
  7. Article
  8. T cell regeneration after immunological injury.Nature reviews. Immunology · 2021
    Review
  9. Interleukin (IL)-7 Signaling in the Tumor Microenvironment.Advances in experimental medicine and biology · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
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

8 authors at 2 institutions in 1 country.

Hye Kyung KimExperimental Transplantation and Immunology Branch, Bethesda, MD, USA.
Adam T WaickmanExperimental Immunology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Ehydel CastroExperimental Transplantation and Immunology Branch, Bethesda, MD, USA.
Francis A FlomerfeltExperimental Transplantation and Immunology Branch, Bethesda, MD, USA.
Nga V HawkExperimental Transplantation and Immunology Branch, Bethesda, MD, USA.
Veena KapoorExperimental Transplantation and Immunology Branch, Bethesda, MD, USA.
William G TelfordExperimental Transplantation and Immunology Branch, Bethesda, MD, USA.
Ronald E GressExperimental Transplantation and Immunology Branch, Bethesda, MD, USA.
American Society of Transplantation · USCenter for Cancer Research · US

Funding

Immune ReconstitutionZIABC010525 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GRESS, RONALD · 2009 to 2023
$21.9M
Transplant ModelsZIABC010957 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GRESS, RONALD · 2009 to 2016
$10.1M
Immune ReconstitutionZ01BC010525 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GRESS, RONALD E. · 2003 to 2008
$4.9M
Intramural NIH HHS Z01 BC010525
6 · The paper itself

Abstract

IL-7 is essential for T-cell survival but its availability is limited in vivo. Consequently, all peripheral T cells, including recent thymic emigrants (RTEs) are constantly competing for IL-7 to survive. RTEs are required to replenish TCR diversity and rejuvenate the peripheral T-cell pool. However, it remains unknown how RTEs successfully compete with resident mature T cells for IL-7. Moreover, RTEs express low levels of IL-7 receptors, presumably rendering them even less competitive. Here, we show that, surprisingly, RTEs are more responsive to IL-7 than mature naïve T cells as demonstrated by markedly increased STAT5 phosphorylation upon IL-7 stimulation. Nonetheless, adoptive transfer of RTE cells into lymphopenic host mice resulted in slower IL-7-induced homeostatic proliferation and diminished expansion compared to naïve donor T cells. Mechanistically, we found that IL-7 signaling in RTEs preferentially upregulated expression of Bcl-2, which is anti-apoptotic but also anti-proliferative. In contrast, naïve T cells showed diminished Bcl-2 induction but greater proliferative response to IL-7. Collectively, these data indicate that IL-7 responsiveness in RTE is designed to maximize survival at the expense of reduced proliferation, consistent with RTE serving as a subpopulation of T cells rich in diversity but not in frequency.

Indexed as

HomeostasisSignal TransductionAnimalsApoptosisCell MovementCell ProliferationCell SurvivalDNA-Binding ProteinsImmunophenotypingInterleukin-7Lymphocyte ActivationMiceMice, KnockoutMice, TransgenicProto-Oncogene Proteins c-bcl-2Receptors, Interleukin-7DNA-Binding ProteinsInterleukin-7Proto-Oncogene Proteins c-bcl-2Rag2 protein, mouseReceptors, Interleukin-7Apoptosis ⋅ Bcl-2 ⋅ Cytokine ⋅ Proliferation ⋅ STAT5

Identifiers

PMID27129922
PMCPMC7780244
OpenAlexW2344270430

What OpenQuestion holds

Textmetadata
LicenceTDM
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.