A H3K27M-targeted vaccine in adults with diffuse midline glioma.


Journal

Nature medicine
ISSN: 1546-170X
Titre abrégé: Nat Med
Pays: United States
ID NLM: 9502015

Informations de publication

Date de publication:
10 2023
Historique:
received: 23 02 2023
accepted: 22 08 2023
medline: 23 10 2023
pubmed: 22 9 2023
entrez: 22 9 2023
Statut: ppublish

Résumé

Substitution of lysine 27 to methionine in histone H3 (H3K27M) defines an aggressive subtype of diffuse glioma. Previous studies have shown that a H3K27M-specific long peptide vaccine (H3K27M-vac) induces mutation-specific immune responses that control H3K27M

Identifiants

pubmed: 37735561
doi: 10.1038/s41591-023-02555-6
pii: 10.1038/s41591-023-02555-6
pmc: PMC10579055
doi:

Substances chimiques

Histones 0
Vaccines 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2586-2592

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2023. The Author(s).

Références

Louis, D. N. et al. The 2021 WHO classification of tumors of the central nervous system: a summary. Neuro. Oncol. 23, 1231–1251 (2021).
doi: 10.1093/neuonc/noab106 pubmed: 34185076 pmcid: 8328013
Bender, S. et al. Reduced H3K27me3 and DNA hypomethylation are major drivers of gene expression in K27M mutant pediatric high-grade gliomas. Cancer Cell 24, 660–672 (2013).
doi: 10.1016/j.ccr.2013.10.006 pubmed: 24183680
Jessa, S. et al. K27M in canonical and noncanonical H3 variants occurs in distinct oligodendroglial cell lineages in brain midline gliomas. Nat. Genet. 54, 1865–1880 (2022).
doi: 10.1038/s41588-022-01205-w pubmed: 36471070 pmcid: 9742294
Liu, I. et al. The landscape of tumor cell states and spatial organization in H3-K27M mutant diffuse midline glioma across age and location. Nat. Genet. 54, 1881–1894 (2022).
doi: 10.1038/s41588-022-01236-3 pubmed: 36471067 pmcid: 9729116
Kramm, C. M. et al. Thalamic high-grade gliomas in children: a distinct clinical subset? Neuro. Oncol. 13, 680–689 (2011).
doi: 10.1093/neuonc/nor045 pubmed: 21636712 pmcid: 3107103
Robison, N. J. & Kieran, M. W. Diffuse intrinsic pontine glioma: a reassessment. J. Neurooncol. 119, 7–15 (2014).
doi: 10.1007/s11060-014-1448-8 pubmed: 24792486
Vuong, H. G., Ngo, T. N. M., Le, H. T. & Dunn, I. F. The prognostic significance of HIST1H3B/C and H3F3A K27M mutations in diffuse midline gliomas is influenced by patient age. J. Neurooncol. 158, 405–412 (2022).
doi: 10.1007/s11060-022-04027-2 pubmed: 35606633
Omuro, A. et al. Nivolumab with or without ipilimumab in patients with recurrent glioblastoma: results from exploratory phase I cohorts of CheckMate 143. Neuro. Oncol. 20, 674–686 (2018).
doi: 10.1093/neuonc/nox208 pubmed: 29106665
Vinci, M. et al. Functional diversity and cooperativity between subclonal populations of pediatric glioblastoma and diffuse intrinsic pontine glioma cells. Nat. Med. 24, 1204–1215 (2018).
doi: 10.1038/s41591-018-0086-7 pubmed: 29967352 pmcid: 6086334
Jha, P. et al. Analysis of PD-L1 expression and T cell infiltration in different molecular subgroups of diffuse midline gliomas. Neuropathology 39, 413–424 (2019).
doi: 10.1111/neup.12594 pubmed: 31625205
Alexandrov, L. B. et al. Signatures of mutational processes in human cancer. Nature 500, 415–421 (2013).
doi: 10.1038/nature12477 pubmed: 23945592 pmcid: 3776390
McGranahan, N. et al. Clonal neoantigens elicit T cell immunoreactivity and sensitivity to immune checkpoint blockade. Science 351, 1463–1469 (2016).
doi: 10.1126/science.aaf1490 pubmed: 26940869 pmcid: 4984254
Touat, M. et al. Mechanisms and therapeutic implications of hypermutation in gliomas. Nature 580, 517–523 (2020).
doi: 10.1038/s41586-020-2209-9 pubmed: 32322066 pmcid: 8235024
Cacciotti, C. et al. Immune checkpoint inhibition for pediatric patients with recurrent/refractory CNS tumors: a single institution experience. J. Neurooncol. 149, 113–122 (2020).
doi: 10.1007/s11060-020-03578-6 pubmed: 32627129
Majzner, R. G. et al. GD2-CAR T cell therapy for H3K27M-mutated diffuse midline gliomas. Nature 603, 934–941 (2022).
doi: 10.1038/s41586-022-04489-4 pubmed: 35130560 pmcid: 8967714
Martínez-Vélez, N. et al. The oncolytic virus Delta-24-RGD elicits an antitumor effect in pediatric glioma and DIPG mouse models. Nat. Commun. 10, 2235 (2019).
doi: 10.1038/s41467-019-10043-0 pubmed: 31138805 pmcid: 6538754
Mueller, S. et al. Mass cytometry detects H3.3K27M-specific vaccine responses in diffuse midline glioma. J. Clin. Invest. 130, 6325–6337 (2020).
doi: 10.1172/JCI140378 pubmed: 32817593 pmcid: 7685729
Ochs, K. et al. K27M-mutant histone-3 as a novel target for glioma immunotherapy. Oncoimmunology 6, e1328340 (2017).
doi: 10.1080/2162402X.2017.1328340 pubmed: 28811969 pmcid: 5543817
Immisch, L. et al. H3.3K27M mutation is not a suitable target for immunotherapy in HLA-A2
Platten, M. et al. A vaccine targeting mutant IDH1 in newly diagnosed glioma. Nature 592, 463–468 (2021).
doi: 10.1038/s41586-021-03363-z pubmed: 33762734 pmcid: 8046668
Schumacher, T. et al. A vaccine targeting mutant IDH1 induces antitumour immunity. Nature 512, 324–327 (2014).
doi: 10.1038/nature13387 pubmed: 25043048
Kilian, M. et al. MHC class II-restricted antigen presentation is required to prevent dysfunction of cytotoxic T cells by blood-borne myeloids in brain tumors. Cancer Cell 41, 235–251 (2023).
doi: 10.1016/j.ccell.2022.12.007 pubmed: 36638785
Bunse, L. et al. Suppression of antitumor T cell immunity by the oncometabolite (R)-2-hydroxyglutarate. Nat. Med. 24, 1192–1203 (2018).
doi: 10.1038/s41591-018-0095-6 pubmed: 29988124
Reardon, D. A. et al. Rindopepimut with bevacizumab for patients with relapsed EGFRvIII-expressing glioblastoma (ReACT): results of a double-blind randomized phase II trial. Clin. Cancer Res. 26, 1586–1594 (2020).
doi: 10.1158/1078-0432.CCR-18-1140 pubmed: 32034072
Weller, M. et al. Rindopepimut with temozolomide for patients with newly diagnosed, EGFRvIII-expressing glioblastoma (ACT IV): a randomised, double-blind, international phase 3 trial. Lancet Oncol. 18, 1373–1385 (2017).
doi: 10.1016/S1470-2045(17)30517-X pubmed: 28844499
Goff, S. L. et al. Pilot trial of adoptive transfer of chimeric antigen receptor-transduced T cells targeting EGFRvIII in patients with glioblastoma. J. Immunother. 42, 126–135 (2019).
doi: 10.1097/CJI.0000000000000260 pubmed: 30882547 pmcid: 6691897
van den Bent, M. J. et al. Changes in the EGFR amplification and EGFRvIII expression between paired primary and recurrent glioblastomas. Neuro. Oncol. 17, 935–941 (2015).
doi: 10.1093/neuonc/nov013 pubmed: 25691693 pmcid: 5762005
Bunse, L. et al. Proximity ligation assay evaluates IDH1R132H presentation in gliomas. J. Clin. Invest. 125, 593–606 (2015).
pubmed: 25555220 pmcid: 4319432
Grant, C. E. & Bailey, T. L. XSTREME: comprehensive motif analysis of biological sequence datasets. Preprint at bioRxiv https://doi.org/10.1101/2021.09.02.458722 (2021).

Auteurs

Niklas Grassl (N)

DKTK CCU Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Department of Neurology, Medical Faculty Mannheim, MCTN, Heidelberg University, Mannheim, Germany.
DKFZ-Hector Cancer Institute at University Medical Center Mannheim, Mannheim, Germany.

Isabel Poschke (I)

DKTK CCU Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Immune Monitoring Unit, German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT), Heidelberg, Germany.

Katharina Lindner (K)

DKTK CCU Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Immune Monitoring Unit, German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT), Heidelberg, Germany.

Lukas Bunse (L)

DKTK CCU Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Department of Neurology, Medical Faculty Mannheim, MCTN, Heidelberg University, Mannheim, Germany.
DKFZ-Hector Cancer Institute at University Medical Center Mannheim, Mannheim, Germany.

Iris Mildenberger (I)

DKTK CCU Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Department of Neurology, Medical Faculty Mannheim, MCTN, Heidelberg University, Mannheim, Germany.
DKFZ-Hector Cancer Institute at University Medical Center Mannheim, Mannheim, Germany.

Tamara Boschert (T)

DKTK CCU Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Immune Monitoring Unit, German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT), Heidelberg, Germany.
Helmholtz Institute for Translational Oncology (HI-TRON) Mainz, German Cancer Research Center, Mainz, Germany.

Kristine Jähne (K)

DKTK CCU Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Department of Neurology, Medical Faculty Mannheim, MCTN, Heidelberg University, Mannheim, Germany.
DKFZ-Hector Cancer Institute at University Medical Center Mannheim, Mannheim, Germany.

Edward W Green (EW)

DKTK CCU Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Department of Neurology, Medical Faculty Mannheim, MCTN, Heidelberg University, Mannheim, Germany.
DKFZ-Hector Cancer Institute at University Medical Center Mannheim, Mannheim, Germany.

Ingrid Hülsmeyer (I)

DKTK CCU Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Immune Monitoring Unit, German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT), Heidelberg, Germany.

Simone Jünger (S)

DKTK CCU Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Immune Monitoring Unit, German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT), Heidelberg, Germany.

Tobias Kessler (T)

Department of Neurology, University Hospital Heidelberg, Heidelberg, Germany.
National Center for Tumor Diseases (NCT), University Hospital Heidelberg, Heidelberg, Germany.

Abigail K Suwala (AK)

Department of Neuropathology, University Hospital Heidelberg, Heidelberg, Germany.
DKTK Clinical Cooperation Unit Neuropathology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Philipp Eisele (P)

Department of Neurology, Medical Faculty Mannheim, MCTN, Heidelberg University, Mannheim, Germany.

Michael O Breckwoldt (MO)

DKTK CCU Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
DKFZ-Hector Cancer Institute at University Medical Center Mannheim, Mannheim, Germany.
Department of Neuroradiology, Heidelberg University Hospital, Heidelberg, Germany.

Peter Vajkoczy (P)

Department of Neurosurgery, Charité-Universitätsmedizin Berlin, Berlin, Germany.

Oliver M Grauer (OM)

Department of Neurology with Institute of Translational Neurology, University of Münster, Münster, Germany.

Ulrich Herrlinger (U)

Division of Clinical Neurooncology, Department of Neurology, University Hospital Bonn, University of Bonn, Bonn, Germany.

Joerg-Christian Tonn (JC)

Department of Neurosurgery, University of Munich LMU, Munich, Germany.

Monika Denk (M)

Institute of Cell Biology, Department of Immunology, University of Tübingen, Tübingen, Germany.

Felix Sahm (F)

Department of Neuropathology, University Hospital Heidelberg, Heidelberg, Germany.
DKTK Clinical Cooperation Unit Neuropathology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Martin Bendszus (M)

Department of Neuroradiology, Heidelberg University Hospital, Heidelberg, Germany.

Andreas von Deimling (A)

Department of Neuropathology, University Hospital Heidelberg, Heidelberg, Germany.
DKTK Clinical Cooperation Unit Neuropathology, German Cancer Research Center (DKFZ), Heidelberg, Germany.

Frank Winkler (F)

Department of Neurology, University Hospital Heidelberg, Heidelberg, Germany.
National Center for Tumor Diseases (NCT), University Hospital Heidelberg, Heidelberg, Germany.

Wolfgang Wick (W)

Department of Neurology, University Hospital Heidelberg, Heidelberg, Germany.
National Center for Tumor Diseases (NCT), University Hospital Heidelberg, Heidelberg, Germany.

Michael Platten (M)

DKTK CCU Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany. m.platten@dkfz-heidelberg.de.
Department of Neurology, Medical Faculty Mannheim, MCTN, Heidelberg University, Mannheim, Germany. m.platten@dkfz-heidelberg.de.
DKFZ-Hector Cancer Institute at University Medical Center Mannheim, Mannheim, Germany. m.platten@dkfz-heidelberg.de.
Immune Monitoring Unit, German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT), Heidelberg, Germany. m.platten@dkfz-heidelberg.de.
Helmholtz Institute for Translational Oncology (HI-TRON) Mainz, German Cancer Research Center, Mainz, Germany. m.platten@dkfz-heidelberg.de.

Katharina Sahm (K)

DKTK CCU Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), Heidelberg, Germany. k.sahm@dkfz-heidelberg.de.
Department of Neurology, Medical Faculty Mannheim, MCTN, Heidelberg University, Mannheim, Germany. k.sahm@dkfz-heidelberg.de.
DKFZ-Hector Cancer Institute at University Medical Center Mannheim, Mannheim, Germany. k.sahm@dkfz-heidelberg.de.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH