Evidence map›Paper›PMID 23851689›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Ndfip1 enforces a requirement for CD28 costimulation by limiting IL-2 production.

Natalia Ramos-Hernández, Hilda E Ramon, Allison M Beal, Ami Laroche, Erin A Dekleva, Paula M Oliver

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Autophagy activation by the Becn1Brain, behavior, and immunity · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
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  9. Article
  10. Article
  11. Increased peripheral IL-4 leads to an expanded virtual memory CD8+ population.Journal of immunology (Baltimore, Md. : 1950) · 2014
    Article
  12. Ndfip1 mediates peripheral tolerance to self and exogenous antigen by inducing cell cycle exit in responding CD4+ T cells.Proceedings of the National Academy of Sciences of the United States of America · 2014
    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

6 authors at 2 institutions in 1 country.

Natalia Ramos-HernándezSchool of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Hilda E Ramon
Allison M Beal
Ami Laroche
Erin A Dekleva
Paula M Oliver
Children's Hospital of Philadelphia · USUniversity of Pennsylvania · US

Funding

Immune System Development and RegulationT32AI055428 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI ALLMAN, DAVID M, OLIVER, PAULA MARIA · 2003 to 2025
$4.2M
Nedd4-family adaptors and their regulation of T cell function.R01AI093566 · NIAID · CHILDREN'S HOSP OF PHILADELPHIA · PI OLIVER, PAULA MARIA · 2011 to 2020
$4.2M
A novel ubiquitin-ligase complex that prevents skin inflammationR03AR057144 · NIAMS · CHILDREN'S HOSP OF PHILADELPHIA · PI OLIVER, PAULA MARIA · 2009 to 2011
$242k
Defining mechanisms for how Ndfip1 regulates T cell-mediated allergic responsesF32AI085837 · NIAID · CHILDREN'S HOSP OF PHILADELPHIA · PI BEAL, ALLISON MARIE · 2010 to 2012
$153k
NIAID NIH HHS 1F32AI085837NIAID NIH HHS F32 AI085837NIAID NIH HHS R01 AI093566NIAID NIH HHS R01AI093566NIAID NIH HHS T32 AI055428NIAMS NIH HHS R03 AR057144
6 · The paper itself

Abstract

Although the pathways that permit IL-2 production and the full activation of T cells upon Ag encounter are fairly well defined, the negative regulatory circuits that limit these pathways are poorly understood. In this study, we show that the E3 ubiquitin ligase adaptor Ndfip1 directs one such negative regulatory circuit. T cells lacking Ndfip1 produce IL-2, upregulate IL-2Rα, and proliferate, in the absence of CD28 costimulation. Furthermore, T cells in mice lacking both Ndfip1 and CD28 become activated, produce IL-4, and drive inflammation at barrier surfaces. Ndfip1 constrains T cell activation by limiting the duration of IL-2 mRNA expression after TCR stimulation. Ndfip1 and IL-2 have a similar expression pattern, and, following TCR stimulation, expression of both Ndfip1 and IL-2 requires the activity of NFAT and Erk. Taken together, these data support a negative regulatory circuit in which factors that induce IL-2 expression downstream of TCR engagement also induce the expression of Ndfip1 to limit the extent of IL-2 production and, thus, dampen T cell activation.

Indexed as

AnimalsAntigen PresentationAntigensCarrier ProteinsCD28 AntigensCD4-Positive T-LymphocytesCells, CulturedCoculture TechniquesCostimulatory and Inhibitory T-Cell ReceptorsCyclosporineFeedback, PhysiologicalGene Expression RegulationHyaluronan ReceptorsIntercellular Signaling Peptides and ProteinsInterleukin-2Interleukin-2 Receptor alpha SubunitAntigensCarrier ProteinsCD28 AntigensCd44 protein, mouseCostimulatory and Inhibitory T-Cell ReceptorsCyclosporineHyaluronan ReceptorsIntercellular Signaling Peptides and ProteinsInterleukin-2Interleukin-2 Receptor alpha SubunitItch protein, mouseMembrane ProteinsNdfip1 protein, mouseNFATC Transcription FactorsOvalbuminProtein Kinase InhibitorsUbiquitin-Protein Ligases

Identifiers

PMID23851689
PMCPMC3853121
OpenAlexW2113002340

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.