Evidence map›Paper›PMID 30425108›Full record

ArticleCancer immunology research2019

Mapping the MHC Class I-Spliced Immunopeptidome of Cancer Cells.

Juliane Liepe, John Sidney, Felix K M Lorenz, Alessandro Sette, Michele Mishto

Abstract read
In one paragraph

Article in Cancer immunology research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
–field-weighted citation impact
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

39 citing papers in PubMed.

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  18. Article
  19. Spliced HLA-bound peptides: a Black Swan event in immunology.Clinical and experimental immunology · 2021
    Review
  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

5 authors.

Juliane LiepeMax Planck Institute for Biophysical Chemistry, Göttingen, Germany. michele.mishto@kcl.ac.uk jliepe@mpibpc.mpg.de.
John SidneyDivision of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, California.
Felix K M LorenzMax-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.ORCID 0000-0001-7826-0839
Alessandro SetteDivision of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, California.
Michele MishtoCentre for Inflammation Biology and Cancer Immunology (CIBCI) and Peter Gorer Department of Immunobiology, King's College London, London, United Kingdom. michele.mishto@kcl.ac.uk jliepe@mpibpc.mpg.de.ORCID 0000-0003-3042-2792

Funding

Development of a pipeline tool to predict immunogenicity of cancer neo-epitopesR21AI134127 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI PETERS, BJOERN, SETTE, ALESSANDRO · 2018 to 2019
$495k
Cancer Research UKNIAID NIH HHS R21 AI134127
6 · The paper itself

Abstract

Anticancer immunotherapies demand optimal epitope targets, which could include proteasome-generated spliced peptides if tumor cells were to present them. Here, we show that spliced peptides are widely presented by MHC class I molecules of colon and breast carcinoma cell lines. The peptides derive from hot spots within antigens and enlarge the antigen coverage. Spliced peptides also represent a large number of antigens that would otherwise be neglected by patrolling T cells. These antigens tend to be long, hydrophobic, and basic. Thus, spliced peptides can be a key to identifying targets in an enlarged pool of antigens associated with cancer.

Indexed as

Antigens, NeoplasmBase SequenceBreast NeoplasmsCell Line, TumorColonic NeoplasmsGenes, MHC Class IHumansPeptidesProtein SplicingAntigens, NeoplasmPeptides

Identifiers

PMID30425108
PMCPMC12032831

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Registered trials

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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.