Evidence map›Paper›PMID 19710470›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

Specific requirements for Vgamma9Vdelta2 T cell stimulation by a natural adenylated phosphoantigen.

Pierre Vantourout, Jayati Mookerjee-Basu, Corinne Rolland, Frédéric Pont, Hélène Martin, Christian Davrinche, Laurent O Martinez, Bertrand Perret, Xavier Collet, Christian Périgaud and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

32 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
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  7. Cell reports methods · 2022
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  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Butyrophilin3A proteins and Vγ9Vδ2 T cell activation.Seminars in cell & developmental biology · 2018
    Review
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  19. Activating and propagating polyclonal gamma delta T cells with broad specificity for malignancies.Clinical cancer research : an official journal of the American Association for Cancer Research · 2014
    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

12 authors at 5 institutions in 3 countries.

Pierre VantouroutDépartement Lipoprotéines et Médiateurs Lipidiques, INSERM, Unité 563, Centre de Physiopathologie de Toulouse Purpan, Université Toulouse III Paul Sabatier, Toulouse, France.
Jayati Mookerjee-Basu
Corinne Rolland
Frédéric Pont
Hélène Martin
Christian Davrinche
Laurent O Martinez
Bertrand Perret
Xavier Collet
Christian Périgaud
Suzanne Peyrottes
Eric Champagne
Lipotec (Spain) · ESCentre National de la Recherche Scientifique · FRUniversité Toulouse III - Paul Sabatier · FRCentre de recherche Translationnelle en Médecine moléculaire · FRProtein Express (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human Vgamma9Vdelta2 T lymphocytes recognize phosphorylated alkyl Ags. Isopentenyl pyrophosphate (IPP) was previously proposed as the main Ag responsible for Vgamma9Vdelta2 T cell activation by cancer cells. However, triphosphoric acid 1-adenosin-5'-yl ester 3-(3-methylbut-3-enyl) ester (ApppI), a metabolite in which the isopentenyl moiety is linked to ATP, was reported in cells activated with aminobisphosphonates. The contribution of this compound to tumor-stimulatory activity was thus examined. ApppI induces selective expansion of Vgamma9Vdelta2 T cells from PBMCs. In the absence of APCs, however, ApppI has little stimulatory activity on Vgamma9Vdelta2 T cells, and optimal activation with ApppI requires addition of a nucleotide pyrophosphatase releasing IPP plus AMP. Thus, ApppI has no intrinsic stimulatory activity. Nevertheless, stimulation by ApppI is strengthened by the presence of APCs. Moreover, in contrast to IPP, ApppI can be efficiently pulsed on dendritic cells as well as on nonprofessional APCs. Pulsed APCs display stable and phosphatase-resistant stimulatory activity, indicative of Ag modification. HPLC analysis of tumor cell extracts indicates that latent phosphoantigenic activity is stored intracellularly in the Vgamma9Vdelta2 cell-sensitive tumor Daudi and can be activated by a nucleotide pyrophosphatase activity. The presence of ApppI in Daudi cell extracts was demonstrated by mass spectrometry. Nucleotidic Ags such as ApppI are thus a storage form of phosphoantigen which may represent a major source of phosphoantigenic activity in tumor cells. The unique properties of ApppI may be important for the design of Ags used in anticancer immunotherapeutic protocols using Vgamma9Vdelta2 cells.

Indexed as

Adenosine MonophosphateAdenosine TriphosphateAntigen-Presenting CellsCell Line, TumorCells, CulturedDiphosphonatesHemiterpenesHumansLymphoma, B-CellOrganophosphorus CompoundsReceptors, Antigen, T-Cell, gamma-deltaT-LymphocytesAdenosine MonophosphateAdenosine TriphosphateDiphosphonatesHemiterpenesisopentenyl pyrophosphateOrganophosphorus CompoundsReceptors, Antigen, T-Cell, gamma-deltaT-cell receptor Vdelta2, humanT-cell receptor Vgamma9, humantriphosphoric acid 1-adenosin-5'-yl ester 3-(3-methylbut-3-enyl) ester

Identifiers

PMID19710470
PMCPMC2809082
OpenAlexW2117375732

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.