TY - JOUR
T1 - De novo H3.3K27M-altered diffuse midline glioma in human brainstem organoids to dissect GD2 CAR T cell function
AU - Bessler, Nils
AU - Wezenaar, Amber K.L.
AU - Ariese, Hendrikus C.R.
AU - Honhoff, Celina
AU - Dommann, Noëlle
AU - Wehrens, Ellen J.
AU - Ruiz Moreno, Cristian
AU - van den Broek, Thijs J.M.
AU - Collot, Raphaël V.U.
AU - Kloosterman, Daan J.
AU - Keramati, Farid
AU - Roosen, Mieke
AU - de Blank, Sam
AU - van Vliet, Esmée
AU - Barrera Román, Mario
AU - Gatti, Lucrezia C.D.E.
AU - Ertürk, Ali
AU - Kuball, Jürgen
AU - Sebestyén, Zsolt
AU - Kool, Marcel
AU - Patrizi, Sara
AU - Miele, Evelina
AU - Künkele, Annette
AU - Kranendonk, Mariëtte E.G.
AU - Cornel, Annelisa M.
AU - Nierkens, Stefan
AU - Mayer, Christian
AU - Stunnenberg, Hendrik G.
AU - Alemany, Anna
AU - Alieva, Maria
AU - Rios, Anne C.
N1 - © 2026. The Author(s).
PY - 2026/2
Y1 - 2026/2
N2 - Diffuse midline glioma (DMG) is a highly aggressive and untreatable pediatric cancer primarily arising in the pontine brainstem region, necessitating the development of representative models for treatment advance. Here we developed an FGF4-driven human brainstem organoid model, which we used to genetically engineer H3.3K27M-altered DMG. We demonstrated that brainstem pontine glial specification is critical for DMG tumorigenesis, yielding infiltrative tumors that recapitulate patient-representative intratumoral heterogeneity. Prolonged GD2 chimeric antigen receptor (CAR) T cell treatment mirrored clinical outcomes and revealed extensive transcriptional heterogeneity, from which both potent effector and dysfunctional CAR T cell populations could be identified. Furthermore, incorporation of myeloid cells generated DMG-specific microglia that reduced treatment efficacy and revealed CAR T cell functional states most vulnerable to microglia-mediated immunosuppression. Thus, we present a representative DMG model offering a months-long experimental window in vitro, which we leveraged to delineate CAR T cell functionality and microglial impact, aiding therapy development for this devastating disease.
AB - Diffuse midline glioma (DMG) is a highly aggressive and untreatable pediatric cancer primarily arising in the pontine brainstem region, necessitating the development of representative models for treatment advance. Here we developed an FGF4-driven human brainstem organoid model, which we used to genetically engineer H3.3K27M-altered DMG. We demonstrated that brainstem pontine glial specification is critical for DMG tumorigenesis, yielding infiltrative tumors that recapitulate patient-representative intratumoral heterogeneity. Prolonged GD2 chimeric antigen receptor (CAR) T cell treatment mirrored clinical outcomes and revealed extensive transcriptional heterogeneity, from which both potent effector and dysfunctional CAR T cell populations could be identified. Furthermore, incorporation of myeloid cells generated DMG-specific microglia that reduced treatment efficacy and revealed CAR T cell functional states most vulnerable to microglia-mediated immunosuppression. Thus, we present a representative DMG model offering a months-long experimental window in vitro, which we leveraged to delineate CAR T cell functionality and microglial impact, aiding therapy development for this devastating disease.
KW - Microglia/immunology
KW - Animals
KW - T-Lymphocytes/immunology
KW - Immunotherapy, Adoptive/methods
KW - Humans
KW - Glioma/genetics
KW - Brain Stem/pathology
KW - Receptors, Chimeric Antigen/immunology
KW - Mice
KW - Organoids/pathology
KW - Brain Stem Neoplasms/genetics
KW - Gangliosides
UR - https://www.scopus.com/pages/publications/105026667992
UR - https://www.mendeley.com/catalogue/fa19ddd5-de90-35a8-b157-66df510c9cce/
U2 - 10.1038/s43018-025-01084-0
DO - 10.1038/s43018-025-01084-0
M3 - Article
C2 - 41492091
AN - SCOPUS:105026667992
SN - 2662-1347
VL - 7
SP - 316
EP - 333
JO - Nature Cancer
JF - Nature Cancer
IS - 2
ER -