Evidence map›Paper›PMID 31530559›Full record

ArticleCancer immunology research2019

Myeloid-Derived Suppressive Cells Promote B cell-Mediated Immunosuppression via Transfer of PD-L1 in Glioblastoma.

Catalina Lee-Chang, Aida Rashidi, Jason Miska, Peng Zhang, Katarzyna C Pituch, David Hou, Ting Xiao, Mariafausta Fischietti, Seong Jae Kang, Christina L Appin and 6 more

Open access · bronzeAbstract 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 123 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed, 1 pooled it
6.7field-weighted citation impact, top 2% 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

123 citing papers in PubMed, 1 synthesis or guideline pooled it, 165 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Humoral immunity in cancer.Signal transduction and targeted therapy · 2026
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  11. Oncolytic virus M1 reinvigorates CD8Cellular & molecular immunology · 2026
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63 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 1 institution in 1 country.

Catalina Lee-ChangDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Aida RashidiDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Jason MiskaDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Peng ZhangDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Katarzyna C PituchDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
David HouDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Ting XiaoDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Mariafausta FischiettiDepartment of Hematology/Oncology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Seong Jae KangDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Christina L AppinDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Craig HorbinskiDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Leonidas C PlataniasDepartment of Hematology/Oncology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Aurora Lopez-RosasDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Yu HanDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Irina V BalyasnikovaDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Maciej S LesniakDepartment of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois. maciej.lesniak@northwestern.edu.
Northwestern University · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Northwestern University Clinical and Translational Science Institute (NUCATS)UL1TR001422 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI D'AQUILA, RICHARD · 2015 to 2023
$56.8M
STINGing GBM: A First-in- Man Clinical Trial in Surgical Resectable Recurrent GBMP50CA221747 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Pouya Jamshidi · 2018 to 2026
$21.4M
Training Program in Translational Brain Tumor ResearchT32CA151022 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Joseph F Costello · 2010 to 2026
$6.6M
Therapeutic Targeting of Malignant Glioma Stem CellsR35CA197725 · NCI · UNIVERSITY OF CHICAGO · PI LESNIAK, MACIEJ S · 2015 to 2021
$6.2M
Regulatory T Cells and Oncolytic Virotherapy of GliomaR01CA122930 · NCI · UNIVERSITY OF CHICAGO · PI LESNIAK, MACIEJ S · 2008 to 2015
$2.5M
Metabolic Control of Immune Suppression in GliomasR01NS093903 · NINDS · UNIVERSITY OF CHICAGO · PI LESNIAK, MACIEJ S · 2015 to 2019
$2.3M
Intranasal Stem-Cell Based Therapy for GlioblastomaR01NS087990 · NINDS · UNIVERSITY OF CHICAGO · PI BALYASNIKOVA, IRINA V · 2014 to 2018
$2.1M
Tissue Factor as a Key Determinant of IDH1 Mutant versus IDH1 Wild-type Glioma Thrombosis and MalignancyR01NS102669 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI HORBINSKI, CRAIG MICHAEL · 2017 to 2021
$1.7M
Regulatory T Cells in Malignant GliomaR01CA138587 · NCI · UNIVERSITY OF CHICAGO · PI LESNIAK, MACIEJ S · 2009 to 2013
$1.6M
NCATS NIH HHS UL1 TR001422NCI NIH HHS P30 CA060553NCI NIH HHS P50 CA221747NCI NIH HHS R01 CA122930NCI NIH HHS R01 CA138587NCI NIH HHS R35 CA197725NCI NIH HHS T32 CA151022NINDS NIH HHS R01 NS087990NINDS NIH HHS R01 NS093903NINDS NIH HHS R01 NS102669
6 · The paper itself

Abstract

The potent immunosuppression induced by glioblastoma (GBM) is one of the primary obstacles to finding effective immunotherapies. One hallmark of the GBM-associated immunosuppressive landscape is the massive infiltration of myeloid-derived suppressor cells (MDSC) and, to a lesser extent, regulatory T cells (Treg) within the tumor microenvironment. Here, we showed that regulatory B cells (Breg) are a prominent feature of the GBM microenvironment in both preclinical models and clinical samples. Forty percent of GBM patients (

Indexed as

AnimalsAntigens, CD20B7-H1 AntigenB-LymphocytesBrain NeoplasmsCell Line, TumorGlioblastomaHumansImmune ToleranceMice, Inbred C57BLMice, KnockoutMyeloid-Derived Suppressor CellsTumor MicroenvironmentAntigens, CD20B7-H1 AntigenCD274 protein, human

Identifiers

PMID31530559
PMCPMC6891201
OpenAlexW2974227664

What OpenQuestion holds

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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.