Evidence map›Paper›PMID 40140675›Full record

ArticleNature communications2025

Spatial mapping of immune cell environments in NF2-related schwannomatosis vestibular schwannoma.

Adam P Jones, Michael J Haley, Miriam H Meadows, Grace E Gregory, Cathal J Hannan, Ana K Simmons, Leoma D Bere, Daniel G Lewis, Pedro Oliveira, Miriam J Smith and 6 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Trial
  2. Article
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  6. Review
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  8. Review
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

16 authors.

Adam P Jones *Division of Immunology, Immunity to Infection and Respiratory Medicine, Faculty of Biology, Medicine & Health, The University of Manchester, Manchester, UK.
Michael J Haley *Division of Immunology, Immunity to Infection and Respiratory Medicine, Faculty of Biology, Medicine & Health, The University of Manchester, Manchester, UK.
Miriam H MeadowsDivision of Immunology, Immunity to Infection and Respiratory Medicine, Faculty of Biology, Medicine & Health, The University of Manchester, Manchester, UK.ORCID http://orcid.org/0000-0002-5063-0161
Grace E GregoryGeoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Northern Care Alliance NHS Foundation Trust, University of Manchester, Manchester, UK.
Cathal J HannanGeoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Northern Care Alliance NHS Foundation Trust, University of Manchester, Manchester, UK.
Ana K SimmonsDivision of Immunology, Immunity to Infection and Respiratory Medicine, Faculty of Biology, Medicine & Health, The University of Manchester, Manchester, UK.ORCID http://orcid.org/0009-0001-2943-6700
Leoma D BereDivision of Immunology, Immunity to Infection and Respiratory Medicine, Faculty of Biology, Medicine & Health, The University of Manchester, Manchester, UK.
Daniel G LewisGeoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Northern Care Alliance NHS Foundation Trust, University of Manchester, Manchester, UK.
Pedro OliveiraDepartment of Pathology, The Christie Hospital, Manchester, UK.
Miriam J SmithGeoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Northern Care Alliance NHS Foundation Trust, University of Manchester, Manchester, UK.ORCID http://orcid.org/0000-0002-3184-0817
Andrew T KingGeoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Northern Care Alliance NHS Foundation Trust, University of Manchester, Manchester, UK.ORCID http://orcid.org/0000-0002-6546-7248
D Gareth R EvansGeoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Northern Care Alliance NHS Foundation Trust, University of Manchester, Manchester, UK.
Pawel PaszekDivision of Immunology, Immunity to Infection and Respiratory Medicine, Faculty of Biology, Medicine & Health, The University of Manchester, Manchester, UK.ORCID http://orcid.org/0000-0002-0363-0716
David BroughGeoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Northern Care Alliance NHS Foundation Trust, University of Manchester, Manchester, UK. David.brough@manchester.ac.uk.ORCID http://orcid.org/0000-0002-2250-2381
Omar N PathmanabanGeoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Northern Care Alliance NHS Foundation Trust, University of Manchester, Manchester, UK. omar.pathmanaban@manchester.ac.uk.ORCID http://orcid.org/0000-0002-5083-9416
Kevin N CouperDivision of Immunology, Immunity to Infection and Respiratory Medicine, Faculty of Biology, Medicine & Health, The University of Manchester, Manchester, UK. kevin.couper@manchester.ac.uk.ORCID http://orcid.org/0000-0003-4659-8960

Funding

DH | National Institute for Health Research (NIHR) IS-BRC-1215-20007DH | National Institute for Health Research (NIHR) NIHR203308RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BB/S019324/1RCUK | Medical Research Council (MRC) MR/T016515/1RCUK | Medical Research Council (MRC) MR/V034650/1
6 · The paper itself

Abstract

NF2-related Schwannomatosis (NF2 SWN) is a rare disease characterised by the growth of multiple nervous system neoplasms, including bilateral vestibular schwannoma (VS). VS tumours are characterised by extensive leucocyte infiltration. However, the immunological landscape in VS and the spatial determinants within the tumour microenvironment that shape the trajectory of disease are presently unknown. In this study, to elucidate the complex immunological networks across VS, we performed imaging mass cytometry (IMC) on clinically annotated VS samples from NF2 SWN patients. We reveal the heterogeneity in neoplastic cell, myeloid cell and T cell populations that co-exist within VS, and that distinct myeloid cell and Schwann cell populations reside within varied spatial contextures across characteristic Antoni A and B histomorphic niches. Interestingly, T-cell populations co-localise with tumour-associated macrophages (TAMs) in Antoni A regions, seemingly limiting their ability to interact with tumorigenic Schwann cells. This spatial landscape is altered in Antoni B regions, where T-cell populations appear to interact with PD-L1

Indexed as

NeurilemmomaNeurofibromatosesNeurofibromatosis 2Neuroma, AcousticSkin NeoplasmsTumor MicroenvironmentAdultB7-H1 AntigenFemaleHumansMaleMiddle AgedMyeloid CellsNeurofibromin 2Schwann CellsT-LymphocytesB7-H1 AntigenNeurofibromin 2NF2 protein, human

Identifiers

PMID40140675
PMCPMC11947219

What Socratic holds

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LicenceCC BY
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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 Socratic graph.