Evidence map›Paper›PMID 31519915›Full record

ArticleNature communications2019

B cells sustain inflammation and predict response to immune checkpoint blockade in human melanoma.

Johannes Griss, Wolfgang Bauer, Christine Wagner, Martin Simon, Minyi Chen, Katharina Grabmeier-Pfistershammer, Margarita Maurer-Granofszky, Florian Roka, Thomas Penz, Christoph Bock and 12 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 263 papers.

0numbers the graph read from it
0cells of the map it votes in
263citing papers in PubMed
17.4field-weighted citation impact, top 1% 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

263 citing papers in PubMed, 366 citations in OpenAlex.

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  9. B cells in cancer: functions, mechanisms and therapeutic advances.Signal transduction and targeted therapy · 2026
    Review
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  11. Humoral immunity in cancer.Signal transduction and targeted therapy · 2026
    Review
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203 more citing papers are in PubMed but not listed here.

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

22 authors at 7 institutions in 5 countries.

Johannes GrissDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria. johannes.griss@meduniwien.ac.at.ORCID http://orcid.org/0000-0003-2206-9511
Wolfgang BauerDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.ORCID http://orcid.org/0000-0002-0155-1176
Christine WagnerDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.
Martin SimonDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.
Minyi ChenDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.
Katharina Grabmeier-PfistershammerDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.
Margarita Maurer-GranofszkyDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.ORCID http://orcid.org/0000-0003-3519-9972
Florian RokaDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.
Thomas PenzCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090, Vienna, Austria.
Christoph BockCeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090, Vienna, Austria.ORCID http://orcid.org/0000-0001-6091-3088
Gao ZhangMolecular & Cellular Oncogenesis Program and Melanoma Research Center, The Wistar Institute, Philadelphia, PA, 19104-4265, USA.ORCID http://orcid.org/0000-0001-8617-8886
Meenhard HerlynMolecular & Cellular Oncogenesis Program and Melanoma Research Center, The Wistar Institute, Philadelphia, PA, 19104-4265, USA.
Katharina GlatzInstitute of Pathology, University Hospital Basel, 4031, Basel, Switzerland.
Heinz LäubliDivision of Medical Oncology, University Hospital Basel, 4031, Basel, Switzerland.ORCID http://orcid.org/0000-0002-8910-5620
Kirsten D MertzInstitute of Pathology, Cantonal Hospital Baselland, 4410, Liestal, Switzerland.
Peter PetzelbauerDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.ORCID http://orcid.org/0000-0001-7080-5259
Thomas WiesnerDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria.
Markus HartlMass Spectrometry Facility, Max F. Perutz Laboratories (MFPL), University of Vienna, Vienna BioCenter (VBC), 1030, Vienna, Austria.ORCID http://orcid.org/0000-0002-4970-7336
Winfried F PicklDivision of Cellular Immunology and Immunohematology, Institute of Immunology, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, 1090, Vienna, Austria.
Rajasekharan SomasundaramMolecular & Cellular Oncogenesis Program and Melanoma Research Center, The Wistar Institute, Philadelphia, PA, 19104-4265, USA.
Peter SteinbergerInstitute of Immunology, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, 1090, Vienna, Austria.ORCID http://orcid.org/0000-0001-6848-4097
Stephan N WagnerDepartment of Dermatology, Medical University of Vienna, 1090, Vienna, Austria. stephan.wagner@meduniwien.ac.at.ORCID http://orcid.org/0000-0003-4941-7029
Medical University of Vienna · ATThe Wistar Institute · USAustrian Academy of Sciences · ATUniversity Hospital of Basel · CHCancer Research Institute of the Slovak Academy of Sciences · SKEuropean Bioinformatics Institute · GBUniversity of Vienna · AT

Funding

Tumor Microenvironment and MetastasisP30CA010815 · NCI · WISTAR INSTITUTE · PI Luis J Montaner · 1985 to 2026
$75.9M
Targeting the MAP and PI3 Kinase Pathways in MelanomaP01CA114046 · NCI · WISTAR INSTITUTE · PI MURPHY, MAUREEN E. · 2008 to 2023
$37.1M
Research Project 2 - Targeting Melanoma Tumor Survival and Apoptotic MachineryU54CA224070 · NCI · WISTAR INSTITUTE · PI Jessie Villanueva · 2017 to 2026
$13.9M
Targeted Combination Therapy for MelanomaP50CA174523 · NCI · WISTAR INSTITUTE · PI HERLYN, MEENHARD F · 2014 to 2018
$11.1M
Austrian Science Fund FWF P 31127NCI NIH HHS P01 CA114046NCI NIH HHS P30 CA010815NCI NIH HHS P50 CA174523NCI NIH HHS U54 CA224070
6 · The paper itself

Abstract

Tumor associated inflammation predicts response to immune checkpoint blockade in human melanoma. Current theories on regulation of inflammation center on anti-tumor T cell responses. Here we show that tumor associated B cells are vital to melanoma associated inflammation. Human B cells express pro- and anti-inflammatory factors and differentiate into plasmablast-like cells when exposed to autologous melanoma secretomes in vitro. This plasmablast-like phenotype can be reconciled in human melanomas where plasmablast-like cells also express T cell-recruiting chemokines CCL3, CCL4, CCL5. Depletion of B cells in melanoma patients by anti-CD20 immunotherapy decreases tumor associated inflammation and CD8

Indexed as

Antibodies, MonoclonalB-LymphocytesCD8-Positive T-LymphocytesCell Line, TumorChemokine CCL3Chemokine CCL4Chemokine CCL5HumansImmunotherapyInflammationIn Vitro TechniquesMelanomaProgrammed Cell Death 1 ReceptorAntibodies, MonoclonalChemokine CCL3Chemokine CCL4Chemokine CCL5Programmed Cell Death 1 Receptor

Identifiers

PMID31519915
PMCPMC6744450
OpenAlexW2973051889

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.