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      The tumor micro-environment in pediatric glioma: friend or foe?

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          Abstract

          Brain tumors are the leading cause of morbidity and mortality related to cancer in children, where high-grade glioma harbor the worst prognosis. It has become obvious that pediatric glioma differs significantly from their adult counterparts, rendering extrapolations difficult. Curative options for several types of glioma are lacking, albeit ongoing research efforts and clinical trials. As already proven in the past, inter- and intratumoral heterogeneity plays an important role in the resistance to therapy and thus implicates morbidity and mortality for these patients. However, while less studied, the tumor micro-environment (TME) adds another level of heterogeneity. Knowledge gaps exist on how the TME interacts with the tumor cells and how the location of the various cell types in the TME influences tumor growth and the response to treatment. Some studies identified the presence of several (immune) cell types as prognostic factors, but often lack a deeper understanding of the underlying mechanisms, possibly leading to contradictory findings. Although the TME in pediatric glioma is regarded as “cold”, several treatment options are emerging, with the TME being the primary target of treatment. Therefore, it is crucial to study the TME of pediatric glioma, so that the interactions between TME, tumoral cells and therapeutics can be better understood before, during and after treatment. In this review, we provide an overview of the available insights into the composition and role of the TME across different types of pediatric glioma. Moreover, where possible, we provide a framework on how a particular TME may influence responses to conventional- and/or immunotherapy.

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          PD-1 Blockade in Tumors with Mismatch-Repair Deficiency.

          Somatic mutations have the potential to encode "non-self" immunogenic antigens. We hypothesized that tumors with a large number of somatic mutations due to mismatch-repair defects may be susceptible to immune checkpoint blockade.
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            TGF-β attenuates tumour response to PD-L1 blockade by contributing to exclusion of T cells

            Therapeutic antibodies that block the programmed death-ligand 1 (PD-L1)/programmed death-1 (PD-1) pathway can induce robust and durable responses in patients with various cancers, including metastatic urothelial cancer (mUC) 1–5 . However, these responses only occur in a subset of patients. Elucidating the determinants of response and resistance is key to improving outcomes and developing new treatment strategies. Here, we examined tumours from a large cohort of mUC patients treated with an anti–PD-L1 agent (atezolizumab) and identified major determinants of clinical outcome. Response was associated with CD8+ T-effector cell phenotype and, to an even greater extent, high neoantigen or tumour mutation burden (TMB). Lack of response was associated with a signature of transforming growth factor β (TGF-β) signalling in fibroblasts, particularly in patients with CD8+ T cells that were excluded from the tumour parenchyma and instead found in the fibroblast- and collagen-rich peritumoural stroma—a common phenotype among patients with mUC. Using a mouse model that recapitulates this immune excluded phenotype, we found that therapeutic administration of a TGF-β blocking antibody together with anti–PD-L1 reduced TGF-β signalling in stromal cells, facilitated T cell penetration into the centre of the tumour, and provoked vigorous anti-tumour immunity and tumour regression. Integration of these three independent biological features provides the best basis for understanding outcome in this setting and suggests that TGF-β shapes the tumour microenvironment to restrain anti-tumour immunity by restricting T cell infiltration.
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              CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2011–2015

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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                13 October 2023
                2023
                : 14
                : 1227126
                Affiliations
                [1] 1Department of Pediatrics, University Hospitals Leuven , Leuven, Belgium
                [2] 2Laboratory for Precision Cancer Medicine, Translational Cell and Tissue Research, Department of Imaging and Pathology, KU Leuven , Leuven, Belgium
                [3] 3Pediatric Oncology, Department of Oncology, KU Leuven , Leuven, Belgium
                Author notes

                Edited by: Carmen Salguero Aranda, Spanish National Research Council (CSIC), Spain

                Reviewed by: Pengping Li, Xiaoshan Affiliated Hospital of Wenzhou Medical University, China; Ana Teresa Amaral, University of Coimbra, Portugal

                *Correspondence: Frederik De Smet, Frederik.desmet@ 123456kuleuven.be
                Article
                10.3389/fimmu.2023.1227126
                10611473
                37901250
                40dbd4a0-4637-455c-8a23-76d856a9fead
                Copyright © 2023 Messiaen, Jacobs and De Smet

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 22 May 2023
                : 27 September 2023
                Page count
                Figures: 1, Tables: 3, Equations: 0, References: 113, Pages: 15, Words: 8000
                Funding
                Funded by: Fonds Wetenschappelijk Onderzoek , doi 10.13039/501100003130;
                Funded by: KU Leuven , doi 10.13039/501100004040;
                Funded by: Kom op tegen Kanker , doi 10.13039/501100011851;
                Funded by: Olivia Fund , doi 10.13039/100020345;
                JM is funded by the Research Foundation Flanders (grant number 1156522N) and the Olivia Hendrickx Research Fund. This research was further granted KULeuven grant (C14/17/084) en Kom op tegen kanker (Stand up against Cancer).
                Categories
                Immunology
                Review
                Custom metadata
                Cancer Immunity and Immunotherapy

                Immunology
                pediatric glioma,tumor micro-environment,t-cells,myeloid cells,immunotherapy
                Immunology
                pediatric glioma, tumor micro-environment, t-cells, myeloid cells, immunotherapy

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