Evidence map›Paper›PMID 41576930›Full record

ArticleCancer cell2026

IGSF11-VISTA is a critical and targetable immune checkpoint axis in diffuse midline glioma.

Raphaël Collot, Cristian Ruiz-Moreno, Celina Honhoff, Thijs J M van den Broek, Amber K L Wezenaar, Daan J Kloosterman, Hendrikus C R Ariese, Hannah Johnson, Britt M T Vervoort, Amal Jeiroshi and 17 more

Abstract read
In one paragraph

Article in Cancer cell, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. 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

27 authors.

Raphaël CollotPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Oncode Institute, Utrecht, the Netherlands.
Cristian Ruiz-MorenoPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Department of Molecular Biology, Faculty of Science, Radboud University, Nijmegen, the Netherlands.
Celina HonhoffPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Oncode Institute, Utrecht, the Netherlands.
Thijs J M van den BroekPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Oncode Institute, Utrecht, the Netherlands.
Amber K L WezenaarPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Oncode Institute, Utrecht, the Netherlands.
Daan J KloostermanPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Oncode Institute, Utrecht, the Netherlands.
Hendrikus C R AriesePrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Oncode Institute, Utrecht, the Netherlands.
Hannah JohnsonPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Oncode Institute, Utrecht, the Netherlands.
Britt M T VervoortPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Oncode Institute, Utrecht, the Netherlands.
Amal JeiroshiPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Jens BuntPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Ravian L van IneveldPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Oncode Institute, Utrecht, the Netherlands.
Emma BokobzaPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Oncode Institute, Utrecht, the Netherlands.
Heggert G RebelPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Oncode Institute, Utrecht, the Netherlands.
Brigit M Te PasPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Femke C A RingnaldaPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Oncode Institute, Utrecht, the Netherlands.
Marc van de WeteringPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Oncode Institute, Utrecht, the Netherlands.
Pierre A RobeDepartment of Neurology and Neurosurgery, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, the Netherlands.
Marcel KoolPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; University Medical Center Utrecht, Utrecht, the Netherlands; Hopp Children's Cancer Center (KiTZ), Heidelberg, Germany; Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ) and German Cancer Research Consortium (DKTK), Heidelberg, Germany.
Jennifer R CochranDepartment of Bioengineering, Stanford University Schools of Engineering and Medicine, Stanford, CA, USA.
Mariëtte E G KranendonkPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Dannis G van VuurdenPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Esther HullemanPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Ellen J WehrensPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Oncode Institute, Utrecht, the Netherlands.
Anoek ZomerPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Oncode Institute, Utrecht, the Netherlands.
Hendrik G StunnenbergPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Department of Molecular Biology, Faculty of Science, Radboud University, Nijmegen, the Netherlands.
Anne C RiosPrincess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands; Oncode Institute, Utrecht, the Netherlands; Department of Biology, Faculty of Science, Utrecht University, Utrecht, the Netherlands. Electronic address: a.c.rios@prinsesmaximacentrum.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diffuse midline glioma (DMG) is an aggressive pediatric brain tumor with no curative treatment, and lacks a comprehensive understanding of immune-tumor cell interactions within their spatial context. Our multi-omics approach, integrating single-nuclei RNA sequencing, spatial transcriptomics, and high-dimensional imaging, utilizes patient samples and an experimental murine DMG model to unveil two spatially distinct regions. MES-patterns are defined by mesenchymal (MES) tumor cells and blood-derived immune cells, whereas AOO-patterns are enriched with astrocyte (AC)-, oligodendrocyte (OC)-, and oligodendrocyte precursor cell (OPC)-like cancer populations, alongside homeostatic-like microglia. The less-studied immune checkpoint, IGSF11, is primarily expressed by AOO-associated cancer cells, while its receptor VISTA is detected mainly in homeostatic microglia. Targeting IGSF11-VISTA results in tumor reduction and survival benefit, mediated by brain-resident microglia and independent of T cell infiltration. This positions IGSF11-VISTA as a promising immune checkpoint treatment axis to harness the local brain immune response against DMG.

Indexed as

B7 AntigensBrain NeoplasmsGliomaMembrane ProteinsAnimalsGene Expression Regulation, NeoplasticHumansImmune Checkpoint InhibitorsMiceMicrogliaB7 AntigensImmune Checkpoint InhibitorsMembrane ProteinsVSIR protein, humancancer-immune landscapediffuse midline gliomaIGSF11-VISTA immune checkpointmicroglia-cancer interactionspatial multi-omics profiling

Identifiers

PMID41576930
PMCPMC12994606

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LicenceCC BY-NC-ND
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Registered trials

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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.