Evidence map›Paper›PMID 30506802›Full record

ArticleBrain pathology (Zurich, Switzerland)2019

Distribution and prognostic impact of microglia/macrophage subpopulations in gliomas.

Pia S Zeiner, Corinna Preusse, Anna Golebiewska, Jenny Zinke, Ane Iriondo, Arnaud Muller, Tony Kaoma, Katharina Filipski, Monika Müller-Eschner, Simon Bernatz and 14 more

Abstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 122 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
122citing 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

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

  1. Pooled it
  2. Review
  3. CD163 Dominance Within Macrophages/Microglia Reflects a Favorable Prognosis in Patients With Glioblastoma.Neuropathology : official journal of the Japanese Society of Neuropathology · 2026
    Article
  4. Article
  5. Article
  6. Immune Subtypes and Survival in Patients with Primary Glioma.medRxiv : the preprint server for health sciences · 2026
    Article
  7. Review
  8. Accumulation of Siglec10European journal of immunology · 2026
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Magnetic resonance imaging-based radiomics for predicting infiltration levels of CD68+ tumor-associated macrophages in glioblastomas.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2025
    Article
  17. Article
  18. Article
  19. Article
  20. Review

62 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

24 authors.

Pia S ZeinerEdinger Institute, Institute of Neurology, Goethe University Frankfurt, Frankfurt am Main, Germany.ORCID 0000-0001-6626-9211
Corinna PreusseDepartment of Neuropathology, Charité Berlin, Berlin, Germany.
Anna GolebiewskaNORLUX Neuro-Oncology Laboratory, Department of Oncology, Luxembourg Institute of Health (LIH), Luxembourg.
Jenny ZinkeEdinger Institute, Institute of Neurology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Ane IriondoEdinger Institute, Institute of Neurology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Arnaud MullerDepartment of Oncology, Luxembourg Institute of Health (LIH), Luxembourg.
Tony KaomaDepartment of Oncology, Luxembourg Institute of Health (LIH), Luxembourg.
Katharina FilipskiEdinger Institute, Institute of Neurology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Monika Müller-EschnerInstitute of Neuroradiology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Simon BernatzEdinger Institute, Institute of Neurology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Anna-Eva BlankEdinger Institute, Institute of Neurology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Peter BaumgartenEdinger Institute, Institute of Neurology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Elena IlinaEdinger Institute, Institute of Neurology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Anne GroteInstitute of Pathology and Neuropathology, Medical University Hannover, Hannover, Germany.
Martin L HansmannSenckenberg Institute of Pathology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Marcel A VerhoffInstitute of Legal Medicine, Goethe University Frankfurt, Frankfurt am Main, Germany.
Kea FranzDr. Senckenberg Institute of Neurooncology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Friedrich FeuerhakeInstitute of Pathology and Neuropathology, Medical University Hannover, Hannover, Germany.
Joachim P SteinbachDr. Senckenberg Institute of Neurooncology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Jörg WischhusenDepartment of Gynecology, University of Wuerzburg, Wuerzburg, Germany.
Werner StenzelDepartment of Neuropathology, Charité Berlin, Berlin, Germany.
Simone P NiclouNORLUX Neuro-Oncology Laboratory, Department of Oncology, Luxembourg Institute of Health (LIH), Luxembourg.
Patrick N HarterEdinger Institute, Institute of Neurology, Goethe University Frankfurt, Frankfurt am Main, Germany.
Michel MittelbronnEdinger Institute, Institute of Neurology, Goethe University Frankfurt, Frankfurt am Main, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While the central nervous system is considered an immunoprivileged site and brain tumors display immunosuppressive features, both innate and adaptive immune responses affect glioblastoma (GBM) growth and treatment resistance. However, the impact of the major immune cell population in gliomas, represented by glioma-associated microglia/macrophages (GAMs), on patients' clinical course is still unclear. Thus, we aimed at assessing the immunohistochemical expression of selected microglia and macrophage markers in 344 gliomas (including gliomas from WHO grade I-IV). Furthermore, we analyzed a cohort of 241 IDH1R132H-non-mutant GBM patients for association of GAM subtypes and patient overall survival. Phenotypical properties of GAMs, isolated from high-grade astrocytomas by CD11b-based magnetic cell sorting, were analyzed by immunocytochemistry, mRNA microarray, qRT-PCR and bioinformatic analyses. A higher amount of CD68-, CD163- and CD206-positive GAMs in the vital tumor core was associated with beneficial patient survival. The mRNA expression profile of GAMs displayed an upregulation of factors that are considered as pro-inflammatory M1 (eg, CCL2, CCL3L3, CCL4, PTGS2) and anti-inflammatory M2 polarization markers (eg, MRC1, LGMN, CD163, IL10, MSR1), the latter rather being associated with phagocytic functions in the GBM microenvironment. In summary, we present evidence that human GBMs contain mixed M1/M2-like polarized GAMs and that the levels of different GAM subpopulations in the tumor core are positively associated with overall survival of patients with IDH1R132H-non-mutant GBMs.

Indexed as

AdultAgedAnimalsAstrocytomaBrain NeoplasmsCell Line, TumorFemaleGlioblastomaGliomaHumansImmunohistochemistryMacrophagesMaleMiceMicrogliaMiddle Agedgliomaglioma-associated microglia and macrophagesimmune polarizationtumor microenvironment

Identifiers

PMID30506802
PMCPMC6849857

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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.