Evidence map›Paper›PMID 23851681›Full record

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

Human invariant NKT cell subsets differentially promote differentiation, antibody production, and T cell stimulation by B cells in vitro.

Shijuan Grace Zeng, Yasmeen G Ghnewa, Vincent P O'Reilly, Victoria G Lyons, Ann Atzberger, Andrew E Hogan, Mark A Exley, Derek G Doherty

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 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

29 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  6. Article
  7. Use of aFrontiers in immunology · 2021
    Article
  8. Review
  9. Article
  10. Invariant Natural Killer T-cell Dynamics in Human Immunodeficiency Virus-associated Tuberculosis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2020
    Article
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  12. Article
  13. Article
  14. Review
  15. Article
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  20. 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 3 institutions in 2 countries.

Shijuan Grace ZengDepartment of Immunology, School of Medicine, Trinity College Dublin, Dublin 8, Ireland.
Yasmeen G Ghnewa
Vincent P O'Reilly
Victoria G Lyons
Ann Atzberger
Andrew E Hogan
Mark A Exley
Derek G Doherty
Trinity College Dublin · IEHarvard University · USSt. Vincent's University Hospital · IE

Funding

Regulation of hepatic NKT cells by CDld+ liver cellsR21CA143748 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI EXLEY, MARK A · 2010 to 2011
$410k
Obesity increased cancer risk by NKT cell depletion (PQ1)R21CA170194 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI EXLEY, MARK A · 2012 to 2013
$400k
NCI NIH HHS CA143748NCI NIH HHS CA170194NCI NIH HHS R21 CA143748NCI NIH HHS R21 CA170194
6 · The paper itself

Abstract

Invariant NK T (iNKT) cells can provide help for B cell activation and Ab production. Because B cells are also capable of cytokine production, Ag presentation, and T cell activation, we hypothesized that iNKT cells will also influence these activities. Furthermore, subsets of iNKT cells based on CD4 and CD8 expression that have distinct functional activities may differentially affect B cell functions. We investigated the effects of coculturing expanded human CD4(+), CD8α(+), and CD4(-)CD8α(-) double-negative (DN) iNKT cells with autologous peripheral B cells in vitro. All iNKT cell subsets induced IgM, IgA, and IgG release by B cells without needing the iNKT cell agonist ligand α-galactosylceramide. Additionally, CD4(+) iNKT cells induced expansions of cells with phenotypes of regulatory B cells. When cocultured with α-galactosylceramide-pulsed B cells, CD4(+) and DN iNKT cells secreted Th1 and Th2 cytokines but at 10-1000-fold lower levels than when cultured with dendritic cells. CD4(+) iNKT cells reciprocally induced IL-4 and IL-10 production by B cells. DN iNKT cells expressed the cytotoxic degranulation marker CD107a upon exposure to B cells. Remarkably, whereas iNKT cell subsets could induce CD40 and CD86 expression by B cells, iNKT cell-matured B cells were unable to drive proliferation of autologous and alloreactive conventional T cells, as seen with B cells cultured in the absence of iNKT cells. Therefore, human CD4(+), CD8α(+), and DN iNKT cells can differentially promote and regulate the induction of Ab and T cell responses by B cells.

Indexed as

Antibody FormationAntigen PresentationAntigens, CDAntigens, CD1dB-LymphocytesCell DegranulationCell DivisionCell LineCells, CulturedCoculture TechniquesCytokinesDendritic CellsGalactosylceramidesGene Expression RegulationHumansImmunologic Memoryalpha-galactosylceramideAntigens, CDAntigens, CD1dCD1D protein, humanCytokinesGalactosylceramides

Identifiers

PMID23851681
PMCPMC4201948
OpenAlexW2153073920

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.