Evidence map›Paper›PMID 30135181›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2018

Cytosolic Processing Governs TAP-Independent Presentation of a Critical Melanoma Antigen.

Nathalie Vigneron, Violette Ferrari, Benoît J Van den Eynde, Peter Cresswell, Ralf M Leonhardt

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  4. Review
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  9. Review
  10. Aptamers: Cutting edge of cancer therapies.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Review
  11. Article
  12. Review
  13. Vaccine-Induced CD8Frontiers in immunology · 2020
    Review
  14. Review
  15. Article
  16. 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

5 authors at 2 institutions in 2 countries.

Nathalie VigneronLudwig Institute for Cancer Research, Brussels B-1200, Belgium.ORCID 0000-0002-2761-2803
Violette FerrariLudwig Institute for Cancer Research, Brussels B-1200, Belgium.
Benoît J Van den EyndeLudwig Institute for Cancer Research, Brussels B-1200, Belgium; Ralf.Leonhardt@yale.edu Peter.Cresswell@yale.edu Benoit.Vandeneynde@bru.licr.org.ORCID 0000-0002-4995-3270
Peter CresswellDepartment of Immunobiology, Yale University, New Haven, CT 06519; and Ralf.Leonhardt@yale.edu Peter.Cresswell@yale.edu Benoit.Vandeneynde@bru.licr.org.ORCID 0000-0003-0540-2351
Ralf M LeonhardtDepartment of Immunobiology, Yale University, New Haven, CT 06519; and Ralf.Leonhardt@yale.edu Peter.Cresswell@yale.edu Benoit.Vandeneynde@bru.licr.org.ORCID 0000-0001-6673-8217
Ludwig Cancer Research · BEYale University · US

Funding

Yale SPORE in Skin CancerP50CA121974 · NCI · YALE UNIVERSITY · PI DAVID F STERN · 2006 to 2026
$43.9M
Quality Control of MHC Class I Restricted Antigen ProcessingR01AI097206 · NIAID · YALE UNIVERSITY · PI CRESSWELL, PETER · 2012 to 2020
$4.1M
High Performance Computing Instrumentation for the Yale Center for Genome AnalysisS10OD030363 · OD · YALE UNIVERSITY · PI MANE, SHRIKANT M · 2022 to 2022
$1.2M
High Performance Computing Instrumentation for the Yale Center for Genome AnalysiS10OD018521 · OD · YALE UNIVERSITY · PI MANE, SHRIKANT M · 2015 to 2015
$890k
Mechanism of amyloid formation during melanosome biogenesisR21AR068518 · NIAMS · YALE UNIVERSITY · PI LEONHARDT, RALF MAX · 2016 to 2017
$405k
NCI NIH HHS P50 CA121974NIAID NIH HHS R01 AI097206NIAMS NIH HHS R21 AR068518NIH HHS S10 OD018521NIH HHS S10 OD030363
6 · The paper itself

Abstract

Cancer immunotherapy has been flourishing in recent years with remarkable clinical success. But as more patients are treated, a shadow is emerging that has haunted other cancer therapies: tumors develop resistance. Resistance is often caused by defects in the MHC class I Ag presentation pathway critical for CD8 T cell-mediated tumor clearance. TAP and tapasin, both key players in the pathway, are frequently downregulated in human cancers, correlating with poor patient survival. Reduced dependence on these factors may promote vaccine efficiency by limiting immune evasion. In this study, we demonstrate that PMEL

Indexed as

AminopeptidasesAntigen PresentationCD8-Positive T-LymphocytesCell Line, TumorCytosolDipeptidyl-Peptidases and Tripeptidyl-PeptidasesEpitopes, T-Lymphocytegp100 Melanoma AntigenHLA-A2 AntigenHumansImmune EvasionImmunotherapy, AdoptiveMelanomaMembrane Transport ProteinsOligopeptidesSerine EndopeptidasesAminopeptidasesDipeptidyl-Peptidases and Tripeptidyl-PeptidasesEpitopes, T-Lymphocytegp100 Melanoma AntigenHLA-A2 AntigenMembrane Transport ProteinsOligopeptidesPMEL protein, humanSerine Endopeptidasestapasintripeptidyl-peptidase 2trypsinogen activation peptideVaccines

Identifiers

PMID30135181
PMCPMC6457910
OpenAlexW2888652304

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.