Evidence map›Paper›PMID 22593613›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2012

An in vivo IL-7 requirement for peripheral Foxp3+ regulatory T cell homeostasis.

Grace Y Kim, Davinna L Ligons, Changwan Hong, Megan A Luckey, Hilary R Keller, Xuguang Tai, Philip J Lucas, Ronald E Gress, Jung-Hyun Park

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

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  11. Unstable FoxP3+ T regulatory cells in NZW mice.Proceedings of the National Academy of Sciences of the United States of America · 2016
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  12. Review
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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

9 authors at 3 institutions in 1 country.

Grace Y KimExperimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Davinna L Ligons
Changwan Hong
Megan A Luckey
Hilary R Keller
Xuguang Tai
Philip J Lucas
Ronald E Gress
Jung-Hyun Park
National Cancer Institute · USNational Institutes of Health · USJohns Hopkins University · US

Funding

Application of Flow Cytometry to Cell BiologyZICBC009255 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CROSSMAN, ASSIATU · 2009 to 2025
$26.4M
Immune ReconstitutionZIABC010525 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GRESS, RONALD · 2009 to 2023
$21.9M
Post-Transcriptional Regulation of Interleukin-7 Receptor ExpressionZIABC011214 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI PARK, JUNG-HYUN · 2009 to 2025
$15.9M
Transplant ModelsZIABC010957 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GRESS, RONALD · 2009 to 2016
$10.1M
Immune Regulatory Roles of Suppressor Of Cytokine Signaling (SOCS) MoleculesZIABC011215 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI PARK, JUNG-HYUN · 2009 to 2025
$6.9M
Intramural NIH HHS Z99 CA999999Intramural NIH HHS ZIA BC011214Intramural NIH HHS ZIA BC011215NCI NIH HHS Y99 CA999999
6 · The paper itself

Abstract

All T cells are dependent on IL-7 for their development and for homeostasis. Foxp3(+) regulatory T cells (Tregs) are unique among T cells in that they are dependent on IL-2. Whether such IL-2 dependency is distinct from or in addition to an IL-7 requirement has been a confounding issue, particularly because of the absence of an adequate experimental system to address this question. In this study, we present a novel in vivo mouse model where IL-2 expression is intact but IL-7 expression was geographically limited to the thymus. Consequently, IL-7 is not available in peripheral tissues. Such mice were generated by introducing a thymocyte-specific IL-7 transgene onto an IL-7 null background. In these mice, T cell development in the thymus, including Foxp3(+) Treg numbers, was completely restored, which correlates with the thymus-specific expression of transgenic IL-7. In peripheral cells, however, IL-7 expression was terminated, which resulted in a general paucity of T cells and a dramatic reduction of Foxp3(+) Treg numbers. Loss of Tregs was further accompanied by a significant reduction in Foxp3(+) expression levels. These data suggest that peripheral IL-7 is not only necessary for Treg survival but also for upregulating Foxp3 expression. Collectively, we assessed the effect of a selective peripheral IL-7 deficiency in the presence of a fully functional thymus, and we document a critical requirement for in vivo IL-7 in T cell maintenance and specifically in Foxp3(+) cell homeostasis.

Indexed as

AnimalsFlow CytometryFluorescent Antibody TechniqueForkhead Transcription FactorsHomeostasisInterleukin-7MiceMice, Inbred C57BLMice, TransgenicReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionT-Lymphocytes, RegulatoryT-Lymphocyte SubsetsForkhead Transcription FactorsFoxp3 protein, mouseInterleukin-7

Identifiers

PMID22593613
PMCPMC3370137
OpenAlexW2124661527

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.