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Gemistocytic tumor cells programmed for glial scarring characterize T cell confinement in IDH-mutant astrocytoma

  • Levi van Hijfte
  • , Marjolein Geurts
  • , Iris de Heer
  • , Santoesha A. Ghisai
  • , Hayri E. Balcioglu
  • , Youri Hoogstrate
  • , Wies R. Vallentgoed
  • , Rania Head
  • , Rosa Luning
  • , Thierry van den Bosch
  • , Bart Westerman
  • , Pieter Wesseling
  • , Johanna A. Joyce
  • , Pim French
  • , Reno Debets

Research output: Contribution to journalArticlepeer-review

5 Citations (Scopus)

Abstract

Isocitrate dehydrogenase 1/2 mutant (IDHmt) astrocytoma is considered a T cell-deprived tumor, yet little is known regarding the phenotypes underlying T cell exclusion. Using bulk, single nucleus and spatial RNA and protein profiling, we demonstrate that a distinct spatial organization underlies T cell confinement to the perivascular space (T cell cuff) in IDHmt astrocytoma. T cell cuffs are uniquely characterized by a high abundance of gemistocytic tumor cells (GTC) in the surrounding stroma. Integrative analysis shows that GTC-high tumors are enriched for lymphocytes and tumor associated macrophages (TAM) and express immune cell migration and activation programs. Specifically, GTCs constitute a distinct sub-cluster of the astrocyte-like tumor cell state that co-localizes with immune reactive TAMs. Neighboring GTCs and TAMs express receptor-ligand pairs characteristic of reactive astrogliosis and glial scarring, such as SPP1/CD44 and IL-1β/IL1R1. Collectively, we reveal that T cell confinement in IDHmt astrocytomas associates with GTC-TAM networks that mimic glial scarring mechanisms.

Original languageEnglish
Article number1156
JournalNature communications
Volume16
Issue number1
DOIs
Publication statusPublished - 29 Jan 2025

Keywords

  • Astrocytoma/genetics
  • T-Lymphocytes/immunology
  • Humans
  • Tumor-Associated Macrophages/immunology
  • Female
  • Male
  • Astrocytes/pathology
  • Mutation
  • Brain Neoplasms/genetics
  • Isocitrate Dehydrogenase/genetics
  • Gliosis/pathology
  • Cell Movement

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