Evidence map›Paper›PMID 26608910›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

The Tumor Antigen NY-ESO-1 Mediates Direct Recognition of Melanoma Cells by CD4+ T Cells after Intercellular Antigen Transfer.

Jean Francois Fonteneau, Fabienne Brilot, Christian Münz, Monique Gannagé

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.6field-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

24 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. NY-ESO-1 antigen: A promising frontier in cancer immunotherapy.Clinical and translational medicine · 2024
    Review
  3. Review
  4. Article
  5. Article
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  8. Article
  9. Article
  10. TCR engineered T cells for solid tumor immunotherapy.Experimental hematology & oncology · 2022
    Review
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  12. Article
  13. Article
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  15. Review
  16. Article
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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

4 authors at 4 institutions in 4 countries.

Jean Francois FonteneauINSERM UMR892, CNRS UMR6299, Université de Nantes, Nantes 44007, France;ORCID http://orcid.org/0000-0002-3284-8319
Fabienne BrilotNeuroimmunology Group, Institute for Neuroscience and Muscle Research, The Kids Research Institute at the Children's Hospital at Westmead, St. Westmead, New South Wales 2145, Australia;
Christian MünzViral Immunobiology, Institute of Experimental Immunology, University of Zürich, Zürich 8006, Switzerland;
Monique GannagéViral Immunobiology, Institute of Experimental Immunology, University of Zürich, Zürich 8006, Switzerland; Department of Pathology and Immunology, School of Medicine, University of Geneva, Geneva 1211, Switzerland; and Division of Rheumatology, Department of Internal Medicine, University Hospital, Geneva 1205, Switzerland monique.ghannage@unige.ch.ORCID http://orcid.org/0000-0003-3533-1937
Centre National de la Recherche Scientifique · FRChildren's Hospital at Westmead · AUUniversity of Geneva · CHUniversity of Zurich · CH

Funding

DC/NK interactions in human secondary lymphoid organsR01CA108609 · NCI · UNIVERSITY OF ZURICH · PI MUNZ, CHRISTIAN · 2004 to 2012
$1.8M
Endogenous MHC class II antigen processing via autophagyR01CA101741 · NCI · UNIVERSITY OF ZURICH · PI MUNZ, CHRISTIAN · 2006 to 2008
$883k
NCI NIH HHS R01 CA101741NCI NIH HHS R01 CA108609NCI NIH HHS R01CA108609
6 · The paper itself

Abstract

NY-ESO-1-specific CD4(+) T cells are of interest for immune therapy against tumors, because it has been shown that their transfer into a patient with melanoma resulted in tumor regression. Therefore, we investigated how NY-ESO-1 is processed onto MHC class II molecules for direct CD4(+) T cell recognition of melanoma cells. We could rule out proteasome and autophagy-dependent endogenous Ag processing for MHC class II presentation. In contrast, intercellular Ag transfer, followed by classical MHC class II Ag processing via endocytosis, sensitized neighboring melanoma cells for CD4(+) T cell recognition. However, macroautophagy targeting of NY-ESO-1 enhanced MHC class II presentation. Therefore, both elevated NY-ESO-1 release and macroautophagy targeting could improve melanoma cell recognition by CD4(+) T cells and should be explored during immunotherapy of melanoma.

Indexed as

Immunotherapy, AdoptiveAcetylcysteineAntigen PresentationAntigens, NeoplasmAutophagyAutophagy-Related Protein 12CD4-Positive T-LymphocytesCell Line, TumorChloroquineDendritic CellsEndocytosisEpitopes, T-LymphocyteHistocompatibility Antigens Class IIHumansLeupeptinsLymphocyte ActivationAcetylcysteineAntigens, NeoplasmATG12 protein, humanAutophagy-Related Protein 12benzyloxycarbonylleucyl-leucyl-leucine aldehydeChloroquineCTAG1B protein, humanEpitopes, T-LymphocyteHistocompatibility Antigens Class IIlactacystinLAMP2 protein, humanLeupeptinsLysosomal-Associated Membrane Protein 2Membrane ProteinsRNA, Small InterferingSmall Ubiquitin-Related Modifier Proteins

Identifiers

PMID26608910
PMCPMC4683358
OpenAlexW2192652320

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.