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Record W4414799658 · doi:10.1093/neuonc/noaf193.014

JS07.6.A AGE-APPROPRIATE MODELS OF PAEDIATRIC BRAIN TUMOURS REVEAL THE INFLUENCE OF AGE ON TUMOUR-IMMUNE INTERACTION.

2025· article· en· W4414799658 on OpenAlexaff
Zahra Abbas, Omar Elaskalani, Sébastien Malinge, Merridee A. Wouters, Jens Truong, Irudayam Maria Johnson, John K. Kuster, Aziza Nassar, Hannah Smolders, Hilary Hii, Anne McDonnell, A. RENDLE SHORT, Meegan Howlett, C L Kleinmann, Nada Jabado, Terrance G. Johns, Misty R. Jenkins, Timothy N. Phoenix, Nicholas G. Gottardo, Rishi S. Kotecha, Laurence C. Cheung, Timo Lassmann, W. Joost Lesterhuis, Raelene Endersby

Bibliographic record

VenueNeuro-Oncology · 2025
Typearticle
Languageen
FieldMedicine
TopicCancer Immunotherapy and Biomarkers
Canadian institutionsMcGill UniversityMcGill Genome CentreJewish General Hospital
Fundersnot available
KeywordsImmune systemCD8Tumor microenvironmentJuvenileImmunotherapyCytotoxic T cellMajor histocompatibility complexCancerGenetically modified mouse

Abstract

fetched live from OpenAlex

Abstract BACKGROUND The developing immune system of a child is distinct to that of an adult. These differences in the immune system are often ignored in preclinical paediatric cancer research, where adult mice are more commonly used, overlooking potential developmental influences on cancer-microenvironment interactions. These influences are of particular importance when testing immunotherapeutic agents for paediatric cancers. MATERIAL AND METHODS Here, we sought to understand the impact of age on brain tumour progression and tumour-immune interactions. To address this, we have developed paediatric brain cancer mouse models which reflect the developing microenvironment in which these tumours arise. Using spectral flow cytometry, RNA sequencing, and immunohistochemistry, we have characterised differences in the tumour-immune microenvironment of multiple orthotopically-implanted murine brain tumour models in juvenile mice compared to adults. RESULTS We found that identical brain tumour cells elicited tumours that grew faster in juvenile mice and had reduced immune cell infiltration compared to adults. Moreover, immune infiltrates were markedly distinct between juvenile and adult mice. Specifically, juvenile mice possessed more naïve-like CD8 T cells and reduced effector, resident, and exhausted-like CD8 T cells. Tumour-associated macrophages in juvenile mice had reduced MHC II expression and appeared polarized towards an anti-inflammatory state, potentially suppressing effective anti-tumour immune responses. Importantly, we demonstrate that repolarisation of macrophages using immune-modulating agents changed the paediatric tumour-infiltrating immune microenvironment towards a more “adult-like state”, that may enhance immunotherapy effectiveness. CONCLUSION Our findings highlight the significant influence of preclinical model age on cancer-microenvironment interactions. Acknowledging the challenge in finding an appropriate match for human development in mice, these data strongly support the use of age-relevant models in preclinical paediatric cancer studies, especially when evaluating agents which target the microenvironment.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Simulation or modeling · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.005
Threshold uncertainty score0.018

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.000
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0010.000
Science and technology studies0.0000.001
Scholarly communication0.0000.001
Open science0.0010.000
Research integrity0.0010.002
Insufficient payload (model declined to judge)0.0050.002

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.020
GPT teacher head0.304
Teacher spread0.284 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designSimulation or modeling
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2025
Admission routes1
Has abstractyes

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