Evidence map›Paper›PMID 18390727›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

ICOS/ICOSL interaction is required for CD4+ invariant NKT cell function and homeostatic survival.

Omid Akbari, Philippe Stock, Everett H Meyer, Gordon J Freeman, Arlene H Sharpe, Dale T Umetsu, Rosemarie H DeKruyff

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

53 citing papers in PubMed, 83 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. CAR-NKT Cells in Asthma: Use of NKT as a Promising Cell for CAR Therapy.Clinical reviews in allergy & immunology · 2024
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. The Infiltration of ICOSPathology oncology research : POR · 2020
    Article
  15. Article
  16. Enhanced oxidative phosphorylation in NKT cells is essential for their survival and function.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  17. Article
  18. Article
  19. Loss of human ICOSL results in combined immunodeficiency.The Journal of experimental medicine · 2018
    Article
  20. Review
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

7 authors at 5 institutions in 2 countries.

Omid AkbariDivision of Immunology, Children's Hospital, Harvard Medical School, Boston, MA, 02115, USA. omid.akbari@childrens.harvard.edu
Philippe Stock
Everett H Meyer
Gordon J Freeman
Arlene H Sharpe
Dale T Umetsu
Rosemarie H DeKruyff
Boston Children's Hospital · USCharité - Universitätsmedizin Berlin · DEDana-Farber Cancer Institute · USHarvard University · USStanford University · US

Funding

Transgenic/KnockoutP01AI056299 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SHARPE, ARLENE H. · 2003 to 2023
$42.5M
MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
Role of NKT cells in airway hyperreactivity & toleranceR01AI066020 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI AKBARI, OMID · 2007 to 2011
$1.6M
Immune Tolerance/Immune Deviation Protect Against AsthmaR01HL069507 · NHLBI · STANFORD UNIVERSITY · PI DEKRUYFF, ROSEMARIE H · 2001 to 2004
$1.4M
NHLBI NIH HHS R01 HL069507NIAID NIH HHS P01 AI056299NIAID NIH HHS P01 AI56299NIAID NIH HHS R01 AI066020NIAID NIH HHS T32 AI007290
6 · The paper itself

Abstract

The development of airway hyperreactivity (AHR), a cardinal feature of asthma, requires the presence of invariant NKT (iNKT) cells. In a mouse model of asthma, we demonstrated that the induction of AHR required ICOS costimulation of iNKT cells. ICOS was highly expressed on both naive and activated iNKT cells, and expression of ICOS was greater on the CD4(+) iNKT than on CD4(-) iNKT cells. Furthermore, the number of CD4(+) iNKT cells was significantly lower in spleens and livers of ICOS(-/-) and ICOSL(-/-) mice, and the remaining iNKT cells in ICOS(-/-) mice were dysfunctional and failed to reconstitute AHR when adoptively transferred into iNKT cell-deficient Jalpha18(-/-) mice. In addition, direct activation of iNKT cells with alpha-GalCer, which induced AHR in wild-type mice, failed to induce AHR in ICOS(-/-) mice. The failure of ICOS(-/-) iNKT cells to induce AHR was due in part to an inability of the ICOS(-/-) iNKT cells to produce IL-4 and IL-13 on activation. Moreover, survival of wild-type iNKT cells transferred into ICOSL(-/-) mice was greatly reduced due to the induction of apoptosis. These results indicate that ICOS costimulation plays a major role in induction of AHR by iNKT cells and is required for CD4(+) iNKT cell function, homeostasis, and survival in the periphery.

Indexed as

Adoptive TransferAnimalsAntigens, Differentiation, T-LymphocyteApoptosisAsthmaBronchial HyperreactivityBronchoalveolar Lavage FluidCD4-Positive T-LymphocytesCytokinesDisease Models, AnimalFemaleInducible T-Cell Co-Stimulator LigandInducible T-Cell Co-Stimulator ProteinLigandsMiceMice, Inbred BALB CAntigens, Differentiation, T-LymphocyteCytokinesIcosl protein, mouseIcos protein, mouseInducible T-Cell Co-Stimulator LigandInducible T-Cell Co-Stimulator ProteinLigandsProteins

Identifiers

PMID18390727
PMCPMC2835525
OpenAlexW2149943357

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.