Evidence map›Paper›PMID 42662577›Full record

ReviewFrontiers in immunology2026

Unconventional guardians of the brain: MAIT cells as emerging players in glioblastoma immunity.

Eleanor M Eddy, Timothy Patton, Alexander D Barrow, Alexandra J Corbett

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Eleanor M EddyDepartment of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, VIC, Australia.
Timothy PattonDepartment of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, VIC, Australia.
Alexander D BarrowDepartment of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, VIC, Australia.
Alexandra J CorbettDepartment of Microbiology and Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, VIC, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastomas (GBM) are an aggressive form of brain cancer with no curative treatment options. While T cell therapies have demonstrated substantial success in combatting blood cancers, their application for solid tumours, including GBM, is hampered by the immunosuppressive tumour microenvironment and scarcity of tumour antigen-specific targets. There is an urgent need to better understand the immune response to GBM to enable the development of new therapeutic approaches. Recently, a resident population of mucosal-associated invariant T (MAIT) cells in the brain has been described, which may perform critical immune surveillance functions. Recent research also suggests that MAIT cells play diverse roles in anti-tumour immunity, and there is much interest in exploring the potential of MAIT cells in immune therapy by harnessing their cytotoxic capacity and tissue homing properties. However, findings on the role of MAIT cells in cancer are conflicting, while many basic questions regarding MAIT-tumour cell interactions remain. Here we review the challenges for GBM treatment, as well as the potential of unconventional T cells in cancer immunotherapy, with a focus on MAIT cells, their potential role in cancer, and their suitability as novel therapeutic targets in solid tumours such as GBM.

Indexed as

BrainBrain NeoplasmsGlioblastomaMucosal-Associated Invariant T CellsAnimalsHumansImmunotherapyTumor MicroenvironmentbrainGBMglioblastomaimmune therapyMAIT cells

Identifiers

PMID42662577
PMCPMC13519977

What OpenQuestion holds

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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.