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Consensus statement on microglial and macrophage functions in gliomas

  • Yuqi Zheng
  • , Islam Alzoubi
  • , Manuel B Graeber
  • , Atul Anand
  • , Lara Barazzuol
  • , Mario Dorostkar
  • , Karl Frontzek
  • , Anna Golebiewska
  • , Costas G Hadjipanayis
  • , Tibor Hortobagyi
  • , Azzam Ismail
  • , Gerard H Jansen
  • , Bozena Kaminska
  • , Daniel Kirschenbaum
  • , Yoshihiro Komohara
  • , Bjarne Winther Kristensen
  • , Kevin S Lee
  • , Emilie Le Rhun
  • , Q Richard Lu
  • , Kaspar Matiasek
  • Christian Mawrin, Alessandro Michelucci, Nicola Montemurro, Marc-André Mouthon, Quan Liu, Regina Reimann, Roman Sankowski, Alejandro Schcolnik-Cabrera, Michael Schulz, Christian M Schürch, Marius Schwabenland, Aurélie Tchoghandjian, Indrė Valiulytė-Simaitė, Mariano S Viapiano, Tobias Weiss, Michael Weller, Max Wintermark

Publikation: Beitrag in Fachzeitschrift (peer-reviewed)Übersichtsartikel

Abstract

This international consensus statement synthesizes key findings on the complex roles of microglia and macrophages (tumor-associated microglia/macrophages or TAMs) in glioma progression and therapeutic resistance. Recent advances have highlighted the cellular, spatial, and temporal heterogeneity of TAMs, their functional plasticity, and the intricate interactions between TAMs, glioma stem cells, and the neuronal microenvironment, challenging the M1/M2 classification paradigm for TAMs in gliomas and other misconceptions. The statement emphasizes that glioma cells manipulate TAMs to suppress anti-tumor functions, while microglia-mediated modulation of neuron-glioma cell interactions promotes tumor progression. Furthermore, glioblastoma-derived extracellular vesicles (EVs) reprogram microglia to support tumor progression, offering novel therapeutic targets. To advance research and develop more effective treatments, the statement advocates for precision therapies targeting specific TAM subsets or functions, the use of bioengineered EVs as a therapeutic approach, and a shift away from simplistic terminology like "M1/M2" and "neuroinflammation". Ultimately, this new understanding can support innovative strategies to modulate the tumor microenvironment, turning immunosuppression into immunostimulation and improving outcomes for patients with glioblastoma and other types of gliomas.

OriginalspracheEnglisch
Aufsatznummer39
FachzeitschriftActa Neuropathologica
Jahrgang151
Ausgabenummer1
DOIs
PublikationsstatusVeröffentlicht - Juni 2026

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