Evidence map›Paper›PMID 31741766›Full record

ArticleOncoimmunology

HVEM has a broader expression than PD-L1 and constitutes a negative prognostic marker and potential treatment target for melanoma.

Nausicaa Malissen, Nicolas Macagno, Samuel Granjeaud, Clémence Granier, Vincent Moutardier, Caroline Gaudy-Marqueste, Nadia Habel, Marion Mandavit, Bernard Guillot, Christine Pasero and 4 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology. 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
1.9field-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

39 citing papers in PubMed, 55 citations in OpenAlex.

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  6. Virus nanotechnology for intratumoural immunotherapy.Nature reviews bioengineering · 2024
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  10. Effect ofInternational journal of molecular sciences · 2024
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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

14 authors at 4 institutions in 1 country.

Nausicaa MalissenTumor Immunology Team, IBISA Immunomonitoring platform, Cancer Research Center of Marseille, INSERM U1068, CNRS U7258, Aix-Marseille University, Institut Paoli-Calmettes, Marseille, France.ORCID 0000-0001-7211-9658
Nicolas MacagnoINSERM, MMG, APHM, CHU Timone, Department of Pathology, Aix Marseille University, Marseille, France.ORCID 0000-0002-9882-2162
Samuel GranjeaudTumor Immunology Team, IBISA Immunomonitoring platform, Cancer Research Center of Marseille, INSERM U1068, CNRS U7258, Aix-Marseille University, Institut Paoli-Calmettes, Marseille, France.ORCID 0000-0001-9245-1535
Clémence GranierUMR_S970, HEGP, Centre de recherche cardio-vasculaire, Paris, France.
Vincent MoutardierAPHM, CHU Nord, Department of Digestive surgery, Aix Marseille University, Marseille, France.
Caroline Gaudy-MarquesteTumor Immunology Team, IBISA Immunomonitoring platform, Cancer Research Center of Marseille, INSERM U1068, CNRS U7258, Aix-Marseille University, Institut Paoli-Calmettes, Marseille, France.ORCID 0000-0001-6955-5117
Nadia HabelINSERM U 1065, Team 1 Nice, Centre Méditerranéen de Médecine Moléculaire, Nice, France.ORCID 0000-0002-4083-8495
Marion MandavitUMR_S970, HEGP, Centre de recherche cardio-vasculaire, Paris, France.
Bernard GuillotDepartment of Dermatology, CHU Montpellier, Montpellier, France.
Christine PaseroTumor Immunology Team, IBISA Immunomonitoring platform, Cancer Research Center of Marseille, INSERM U1068, CNRS U7258, Aix-Marseille University, Institut Paoli-Calmettes, Marseille, France.
Eric TartourUMR_S970, HEGP, Centre de recherche cardio-vasculaire, Paris, France.
Robert BallottiINSERM U 1065, Team 1 Nice, Centre Méditerranéen de Médecine Moléculaire, Nice, France.ORCID 0000-0002-7322-4908
Jean-Jacques GrobTumor Immunology Team, IBISA Immunomonitoring platform, Cancer Research Center of Marseille, INSERM U1068, CNRS U7258, Aix-Marseille University, Institut Paoli-Calmettes, Marseille, France.
Daniel OliveTumor Immunology Team, IBISA Immunomonitoring platform, Cancer Research Center of Marseille, INSERM U1068, CNRS U7258, Aix-Marseille University, Institut Paoli-Calmettes, Marseille, France.
Centre National de la Recherche Scientifique · FRInserm · FRAix-Marseille Université · FRCentre Hospitalier Universitaire de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HVEM (Herpes Virus Entry Mediator) engagement of BTLA (B and T Lymphocyte Attenuator) triggers inhibitory signals in T cells and could play a role in evading antitumor immunity. Here, HVEM expression levels in melanoma metastases were analyzed by immunohistochemistry, correlated with overall survival (OS) in 116 patients, and validated by TCGA transcriptomic data. Coincident expression of HVEM and its ligand BTLA was studied in tumor cells and tumor-infiltrating lymphocytes (TILs) by flow cytometry (n = 21) and immunofluorescence (n = 5). Candidate genes controlling

Indexed as

BTLAHVEM/TNFRSF14melanomaMITFprognosis

Identifiers

PMID31741766
PMCPMC6844309
OpenAlexW2975660480

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.