Evidence map›Paper›PMID 31646100›Full record

ArticleOncoimmunology

Human Mesenchymal glioblastomas are characterized by an increased immune cell presence compared to Proneural and Classical tumors.

Ioannis Kaffes, Frank Szulzewsky, Zhihong Chen, Cameron J Herting, Ben Gabanic, José E Velázquez Vega, Jennifer Shelton, Jeffrey M Switchenko, James L Ross, Leon F McSwain and 12 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 95 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 1 pooled it
10.1field-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

95 citing papers in PubMed, 1 synthesis or guideline pooled it, 155 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Immune Subtypes and Survival in Patients with Primary Glioma.medRxiv : the preprint server for health sciences · 2026
    Article
  9. Article
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  11. Article
  12. Article
  13. Frontiers in immunology · 2026
    Article
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  18. Article
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  20. Review

35 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 8 institutions in 3 countries.

Ioannis KaffesDepartment of Pediatrics, Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA.
Frank SzulzewskyDepartment of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Zhihong ChenDepartment of Pediatrics, Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA.ORCID 0000-0001-7403-7015
Cameron J HertingDepartment of Pediatrics, Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA.
Ben GabanicDepartment of Pediatrics, Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA.
José E Velázquez VegaDepartment of Pathology and Laboratory Medicine, Emory University, Atlanta, GA, USA.
Jennifer SheltonDepartment of Pathology and Laboratory Medicine, Emory University, Atlanta, GA, USA.
Jeffrey M SwitchenkoDepartment of Biostatistics and Bioinformatics, Winship Cancer Institute, Emory University, Atlanta, GA, USA.
James L RossDepartment of Pediatrics, Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA.
Leon F McSwainDepartment of Pediatrics, Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA.
Jason T HuseDepartments of Pathology and Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Bengt WestermarkDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Sven NelanderDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Karin Forsberg-NilssonDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Lene UhrbomDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Naga Prathyusha MaturiDepartment of Immunology, Genetics and Pathology, Science for Life Laboratory, Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Patrick J CiminoDepartment of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Eric C HollandDepartment of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Helmut KettenmannDepartment of Cellular Neurosciences, Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Berlin, Germany.
Cameron W BrennanDepartment of Neurosurgery, Memorial Sloan Kettering Cancer Center, New York City, NY, USA.
Daniel J BratDepartment of Pathology, Northwestern University, Feinberg School of Medicine, Chicago, IL, USA.
Dolores HambardzumyanDepartment of Pediatrics, Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA.ORCID 0000-0003-1975-4665
Emory University · USUppsala University · SEFred Hutch Cancer Center · USMax Delbrück Center · DEMemorial Sloan Kettering Cancer Center · USNorthwestern University · USThe University of Texas MD Anderson Cancer Center · USUniversity of Washington · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Tumor-Associated Macrophages in Vasogenic Cerebral Edema in Brain TumorsR01NS100864 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI Dolores Hambardzumyan · 2017 to 2026
$5.4M
Graduate Training in the Pharmacological StudiesT32GM008602 · NIGMS · EMORY UNIVERSITY · PI HALL, RANDY A. · 1996 to 2021
$5.1M
Non-neoplastic cell types dictate gliomagenesis andU01CA160882 · NCI · EMORY UNIVERSITY · PI HAMBARDZUMYAN, DOLORES, HOLLAND, ERIC C. · 2012 to 2016
$2.8M
Molecular Target Variation Across Environments and at Margins of GlioblastomaR01CA176659 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BRAT, DANIEL J, HADJIPANAYIS, CONSTANTINOS GEORGE · 2013 to 2017
$2.3M
Identification and targeting of mechanisms specific to glioma stem cells in glioblastomaR01CA214928 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BRAT, DANIEL J · 2018 to 2022
$1.8M
The Role of IL-1 in Glioblastoma-Associated Angiogenesis and Tumor ProgressionF31NS106887 · NINDS · EMORY UNIVERSITY · PI HERTING, CAMERON · 2018 to 2019
$83k
The Role of Tumor Associated Macrophages in Pediatric High-Grade GliomaF31CA232531 · NCI · EMORY UNIVERSITY · PI ROSS, JAMES LUKE · 2018 to 2019
$74k
NCI NIH HHS F31 CA232531NCI NIH HHS P30 CA008748NCI NIH HHS R01 CA176659NCI NIH HHS R01 CA214928NCI NIH HHS U01 CA160882NIGMS NIH HHS T32 GM008602NINDS NIH HHS F31 NS106887NINDS NIH HHS R01 NS100864
6 · The paper itself

Abstract

Glioblastoma (GBM) is the most aggressive malignant primary brain tumor in adults, with a median survival of 14.6 months. Recent efforts have focused on identifying clinically relevant subgroups to improve our understanding of pathogenetic mechanisms and patient stratification. Concurrently, the role of immune cells in the tumor microenvironment has received increasing attention, especially T cells and tumor-associated macrophages (TAM). The latter are a mixed population of activated brain-resident microglia and infiltrating monocytes/monocyte-derived macrophages, both of which express ionized calcium-binding adapter molecule 1 (IBA1). This study investigated differences in immune cell subpopulations among distinct transcriptional subtypes of GBM. Human GBM samples were molecularly characterized and assigned to Proneural, Mesenchymal or Classical subtypes as defined by NanoString nCounter Technology. Subsequently, we performed and analyzed automated immunohistochemical stainings for TAM as well as specific T cell populations. The Mesenchymal subtype of GBM showed the highest presence of TAM, CD8

Indexed as

AIF1GlioblastomamacrophagemicroenvironmentsubtypeT cell

Identifiers

PMID31646100
PMCPMC6791439
OpenAlexW2969983729

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.