Evidence map›Paper›PMID 31679017›Full record

ReviewNeuro-oncology2020

Immune biology of glioma-associated macrophages and microglia: functional and therapeutic implications.

Jun Wei, Peiwen Chen, Pravesh Gupta, Martina Ott, Daniel Zamler, Cynthia Kassab, Krishna P Bhat, Michael A Curran, John F de Groot, Amy B Heimberger

Abstract readReview
In one paragraph

Review in Neuro-oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 163 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
163citing papers in PubMed, 1 pooled it
–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

163 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. KITENIN-CCL20 axis is a potential therapeutic target for modulating immunosuppressive tumor microenvironment in glioblastoma.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

103 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

10 authors.

Jun WeiDepartments of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Peiwen ChenCancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Pravesh GuptaTranslational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Martina OttDepartments of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Daniel ZamlerGenomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cynthia KassabDepartments of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Krishna P BhatTranslational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Michael A CurranImmunology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
John F de GrootNeuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Amy B HeimbergerDepartments of Neurosurgery, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Kathrin Milbury · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

CNS immune defenses are marshaled and dominated by brain resident macrophages and microglia, which are the innate immune sentinels and frontline host immune barriers against various pathogenic insults. These myeloid lineage cells are the predominant immune population in gliomas and can constitute up to 30-50% of the total cellular composition. Parenchymal microglial cells and recruited monocyte-derived macrophages from the periphery exhibit disease-specific phenotypic characteristics with spatial and temporal distinctions and are heterogeneous subpopulations based on their molecular signatures. A preponderance of myeloid over lymphoid lineage cells during CNS inflammation, including gliomas, is a contrasting feature of brain immunity relative to peripheral immunity. Herein we discuss glioma-associated macrophage and microglia immune biology in the context of their identity, molecular drivers of recruitment, nomenclature and functional paradoxes, therapeutic reprogramming and polarization strategies, relevant challenges, and our perspectives on therapeutic modulation.

Indexed as

AnimalsBrain NeoplasmsGliomaHumansMacrophagesMicrogliagliomaimmune suppressionmacrophagesmicroglia

Identifiers

PMID31679017
PMCPMC7442334

What OpenQuestion holds

Textmetadata
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.