Evidence map›Paper›PMID 40787444›Full record

ReviewFrontiers in immunology2025

Harnessing innate immunity against glioblastoma microenvironment.

Wenbo Zhang, Wanhong Zhang, Henghao Wu, Xinsheng Han

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–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

9 citing papers in PubMed.

  1. Review
  2. Targeting the COX-2/PGECancer immunology, immunotherapy : CII · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
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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

4 authors.

Wenbo Zhang *Department of Neurology, Kaifeng Central Hospital, Xinxiang Medical University, Kaifeng, China.
Wanhong Zhang *Department of Neurosurgery, Kaifeng Central Hospital, Kaifeng, China.
Henghao WuDepartment of Neurosurgery, Kaifeng Central Hospital, Kaifeng, China.
Xinsheng HanDepartment of Neurology, Kaifeng Central Hospital, Kaifeng, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) possesses a profoundly immunosuppressive tumor microenvironment (TME) dominated by innate immune mechanisms. Tumor-associated macrophages (TAMs), microglia, and myeloid-derived suppressor cells (MDSCs) constitute the major immunosuppressive axis, promoting tumor progression through cytokine secretion (IL-10, TGF-β), metabolic reprogramming, and inhibition of cytotoxic immunity. These innate immune cells not only facilitate immune evasion but also impair adaptive T-cell responses, limiting the efficacy of current immunotherapies. Emerging evidence highlights the therapeutic potential of targeting innate immunity via TAM repolarization, MDSC depletion, and NK cell activation to reshape the immunosuppressive TME. This review summarizes the pivotal role of innate immunity in GBM pathogenesis and explores novel combinatorial strategies that integrate innate immune modulation with checkpoint blockade, oncolytic virotherapy, and metabolic interventions to overcome therapeutic resistance in this lethal malignancy.

Indexed as

Brain NeoplasmsGlioblastomaImmunity, InnateTumor MicroenvironmentAnimalsHumansImmunotherapyMyeloid-Derived Suppressor CellsOncolytic VirotherapyTumor-Associated Macrophagesglioblastomaimmunotherapyinnate immunitymicrogliamyeloidderived suppressor cellsNK celltumor-associated macrophagestumor microenvironment

Identifiers

PMID40787444
PMCPMC12331708

What OpenQuestion holds

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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.