Evidence map›Paper›PMID 21364749›Full record

ArticlePloS one2011

Protective effector memory CD4 T cells depend on ICOS for survival.

Tamson V Moore, Bryan S Clay, Caroline M Ferreira, Jesse W Williams, Magdalena Rogozinska, Judy L Cannon, Rebecca A Shilling, Amanda L Marzo, Anne I Sperling

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. 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
0.5field-weighted citation impact, top 37% 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, 30 citations in OpenAlex.

  1. Trial
  2. Article
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  7. Review
  8. Article
  9. Cutting Edge: ICOS-Deficient Regulatory T Cells Display Normal Induction ofJournal of immunology (Baltimore, Md. : 1950) · 2019
    Article
  10. Review
  11. CD3Clinical and experimental medicine · 2016
    Article
  12. Loss of Immune Tolerance Is Controlled by ICOS in Sle1 Mice.Journal of immunology (Baltimore, Md. : 1950) · 2016
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  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

9 authors at 3 institutions in 1 country.

Tamson V MooreCommittee on Immunology & Section of Pulmonary and Critical Care Medicine, Department of Medicine, The University of Chicago, Chicago, Illinois, United States of America.
Bryan S Clay
Caroline M Ferreira
Jesse W Williams
Magdalena Rogozinska
Judy L Cannon
Rebecca A Shilling
Amanda L Marzo
Anne I Sperling
University of Chicago · USRush University · USRush University Medical Center · US

Funding

INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007090 · NIAID · UNIVERSITY OF CHICAGO · PI Peter Aidan Savage · 1985 to 2026
$11.7M
Regulation and expression of HLA-G in asthmatic airwaysU19AI095230 · NIAID · UNIVERSITY OF CHICAGO · PI OBER, CAROLE, WHITE, STEVEN R · 2011 to 2016
$10.5M
Molecular Mechanisms of AsthmaP01AI056352 · NIAID · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2003 to 2007
$5.6M
Mechanisms of Resolution in Experimental AsthmaR01AI067697 · NIAID · UNIVERSITY OF CHICAGO · PI SPERLING, ANNE I. · 2007 to 2011
$1.9M
ICOS Expression Levels and Th DevelopmentK08AI059105 · NIAID · UNIVERSITY OF CHICAGO · PI SHILLING, REBECCA A. · 2006 to 2010
$576k
NIAID NIH HHS 5T32AI07090NIAID NIH HHS K08 AI059105NIAID NIH HHS P01 AI056352NIAID NIH HHS P01-AI56352NIAID NIH HHS R01 AI067697NIAID NIH HHS R01 AI67697NIAID NIH HHS T32 AI007090NIAID NIH HHS U19 AI095230
6 · The paper itself

Abstract

Memory CD4 T cells play a vital role in protection against re-infection by pathogens as diverse as helminthes or influenza viruses. Inducible costimulator (ICOS) is highly expressed on memory CD4 T cells and has been shown to augment proliferation and survival of activated CD4 T cells. However, the role of ICOS costimulation on the development and maintenance of memory CD4 T cells remains controversial. Herein, we describe a significant defect in the number of effector memory (EM) phenotype cells in ICOS(-/-) and ICOSL(-/-) mice that becomes progressively more dramatic as the mice age. This decrease was not due to a defect in the homeostatic proliferation of EM phenotype CD4 T cells in ICOS(-/-) or ICOSL(-/-) mice. To determine whether ICOS regulated the development or survival of EM CD4 T cells, we utilized an adoptive transfer model. We found no defect in development of EM CD4 T cells, but long-term survival of ICOS(-/-) EM CD4 T cells was significantly compromised compared to wild-type cells. The defect in survival was specific to EM cells as the central memory (CM) ICOS(-/-) CD4 T cells persisted as well as wild type cells. To determine the physiological consequences of a specific defect in EM CD4 T cells, wild-type and ICOS(-/-) mice were infected with influenza virus. ICOS(-/-) mice developed significantly fewer influenza-specific EM CD4 T cells and were more susceptible to re-infection than wild-type mice. Collectively, our findings demonstrate a role for ICOS costimulation in the maintenance of EM but not CM CD4 T cells.

Indexed as

AnimalsAntigens, Differentiation, T-LymphocyteCD4-Positive T-LymphocytesCell SurvivalCytoprotectionGenetic Predisposition to DiseaseImmunologic MemoryInducible T-Cell Co-Stimulator LigandInducible T-Cell Co-Stimulator ProteinInfluenza A virusInterleukin-4MiceMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutOrthomyxoviridae InfectionsAntigens, Differentiation, T-LymphocyteIcosl protein, mouseIcos protein, mouseInducible T-Cell Co-Stimulator LigandInducible T-Cell Co-Stimulator ProteinInterleukin-4Proteins

Identifiers

PMID21364749
PMCPMC3041765
OpenAlexW1991347309

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.