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

Jones, A. P.
Haley, M. J.
Meadows, M. H.
Gregory, G. E.
Hannan, C. J.
Simmons, A. K.
Bere, L. D.
Lewis, D. G.
Oliveira, P.
Smith, M. J.
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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(+) Schwann cells. We also demonstrate that prior bevacizumab treatment (VEGF-A antagonist) preferentially reduces alternatively activated-like TAMs, whilst enhancing CD44 expression, in bevacizumab-treated tumours. Together, we describe niche-dependent modes of T-cell regulation in NF2 SWN VS, indicating the potential for microenvironment-altering therapies for VS.
Affiliation
Division of Immunology, Immunity to Infection and Respiratory Medicine, Faculty of Biology, Medicine & Health, The University of Manchester, Manchester, UK. Geoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Northern Care Alliance NHS Foundation Trust, University of Manchester, Manchester, UK. Division of Neuroscience, Faculty of Biology, Medicine & Health, The University of Manchester, Manchester, UK. Department of Neurosurgery, Manchester Centre for Clinical Neurosciences, Salford Royal Hospital NHS Foundation Trust, Salford, UK. Department of Pathology, The Christie Hospital, Manchester, UK. Division of Evolution, Infection and Genomics, Faculty of Biology, Medicine & Health, The University of Manchester, Manchester, UK. Department of Biosystems and Soft Matter, Institute of Fundamental Technological Research, Polish Academy of Sciences, Warsaw, Poland. Geoffrey 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. Division of Neuroscience, Faculty of Biology, Medicine & Health, The University of Manchester, Manchester, UK. David.brough@manchester.ac.uk. Geoffrey 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. Division of Neuroscience, Faculty of Biology, Medicine & Health, The University of Manchester, Manchester, UK. omar.pathmanaban@manchester.ac.uk. Department of Neurosurgery, Manchester Centre for Clinical Neurosciences, Salford Royal Hospital NHS Foundation Trust, Salford, UK. omar.pathmanaban@manchester.ac.uk. Division of Immunology, Immunity to Infection and Respiratory Medicine, Faculty of Biology, Medicine & Health, The University of Manchester, Manchester, UK. kevin.couper@manchester.ac.uk. Geoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Northern Care Alliance NHS Foundation Trust, University of Manchester, Manchester, UK. kevin.couper@manchester.ac.uk.
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2025
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Jones AP, Haley MJ, Meadows MH, Gregory GE, Hannan CJ, Simmons AK, et al. Spatial mapping of immune cell environments in NF2-related schwannomatosis vestibular schwannoma. Nature communications. 2025 Mar 26;16(1):2944. PubMed PMID: 40140675. Pubmed Central PMCID: PMC11947219. Epub 2025/03/27. eng.
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