Evidence map›Paper›PMID 31690954›Full record

ArticleCancer immunology, immunotherapy : CII2019

Predominance of M2 macrophages in gliomas leads to the suppression of local and systemic immunity.

Aurobind Vidyarthi, Tapan Agnihotri, Nargis Khan, Sanpreet Singh, Manoj K Tewari, Bishan D Radotra, Deepyan Chatterjee, Javed N Agrewala

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 4% 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

100 citing papers in PubMed, 1 synthesis or guideline pooled it, 138 citations in OpenAlex.

  1. Pooled it
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  7. Article
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  11. ApoE Inhibits the Progression of Glioma by Activating Immune Function.Journal of cellular and molecular medicine · 2025
    Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Immunotherapy in Glioblastoma.Cancer treatment and research · 2025
    Review
  19. Inflammatory factors collaboratively linkFrontiers in immunology · 2025
    Review
  20. Interactions between glioblastoma and myeloid cells.Frontiers in cell and developmental biology · 2025
    Review

40 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

8 authors at 4 institutions in 3 countries.

Aurobind VidyarthiImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, India.
Tapan AgnihotriImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, India.
Nargis KhanImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, India.
Sanpreet SinghImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, India.
Manoj K TewariDepartment of Neurosurgery, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Bishan D RadotraDepartment of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Deepyan ChatterjeeImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, India.
Javed N AgrewalaImmunology Laboratory, CSIR-Institute of Microbial Technology, Chandigarh, India. jagrewala@iitrpr.ac.in.
Institute of Microbial Technology · INPost Graduate Institute of Medical Education and Research · INChristie (Canada) · CAMcGill University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma is a highly prevalent and aggressive form of primary brain tumor. It represents approximately 56% of all the newly diagnosed gliomas. Macrophages are one of the major constituents of tumor-infiltrating immune cells in the human gliomas. The role of immunosuppressive macrophages is very well documented in correlation with the poor prognosis of patients suffering from breast, prostate, bladder and cervical cancers. The current study highlights the correlation between the tumor-associated macrophage phenotypes and glioma progression. We observed an increase in the pool of M2 macrophages in high-grade gliomas, as confirmed by their CD68 and CD163 double-positive phenotype. In contrast, less M1 macrophages were noticed in high-grade gliomas, as evidenced by the down-regulation in the expression of CCL3 marker. In addition, we observed that higher gene expression ratio of CD163/CCL3 is associated with glioma progression. The Kaplan-Meier survival plots indicate that glioma patients with lower expression of M2c marker (CD163), and higher expression of M1 marker (CCL3) had better survival. Furthermore, we examined the systemic immune response in the peripheral blood and noted a predominance of M2 macrophages, myeloid-derived suppressor cells and PD-1

Indexed as

Antigens, CDAntigens, Differentiation, MyelomonocyticBrain NeoplasmsCarcinogenesisCD163 AntigenCD4-Positive T-LymphocytesCD68 MoleculeChemokine CCL3CytokinesDisease ProgressionGene Expression Regulation, NeoplasticGlioblastomaHumansImmune ToleranceImmunity, HumoralMacrophagesAntigens, CDAntigens, Differentiation, MyelomonocyticCD163 AntigenCD68 antigen, humanCD68 MoleculeChemokine CCL3CytokinesPDCD1 protein, humanProgrammed Cell Death 1 ReceptorReceptors, Cell SurfaceCCL3CD163GliomaPD-1Tumor-associated macrophages

Identifiers

PMID31690954
PMCPMC11028103
OpenAlexW2984698492

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.