Site-Specific Considerations on Engineered T Cells for Malignant Gliomas.

CAR T cells CARs FUS glioblastoma glioma intrathecal delivery nanotechnology systemic delivery

Journal

Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304

Informations de publication

Date de publication:
19 Jul 2022
Historique:
received: 19 06 2022
revised: 14 07 2022
accepted: 16 07 2022
entrez: 27 7 2022
pubmed: 28 7 2022
medline: 28 7 2022
Statut: epublish

Résumé

Immunotherapy has revolutionized cancer treatment. Despite the recent advances in immunotherapeutic approaches for several tumor entities, limited response has been observed in malignant gliomas, including glioblastoma (GBM). Conversely, one of the emerging immunotherapeutic modalities is chimeric antigen receptors (CAR) T cell therapy, which demonstrated promising clinical responses in other solid tumors. Current pre-clinical and interventional clinical studies suggest improved efficacy when CAR-T cells are delivered locoregionally, rather than intravenously. In this review, we summarize possible CAR-T cell administration routes including locoregional therapy, systemic administration with and without focused ultrasound, direct intra-arterial drug delivery and nanoparticle-enhanced delivery in glioma. Moreover, we discuss published as well as ongoing and planned clinical trials involving CAR-T cell therapy in malignant glioma. With increasing neoadjuvant and/or adjuvant combinatorial immunotherapeutic concepts and modalities with specific modes of action for malignant glioma, selection of administration routes becomes increasingly important.

Identifiants

pubmed: 35885047
pii: biomedicines10071738
doi: 10.3390/biomedicines10071738
pmc: PMC9312945
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : Helmholtz Gemeinschaft, Zukun-ftsthema "Immunology and Infection"
ID : ZT0027, WP3
Organisme : the German Research Foundation
ID : Project ID 404521405
Organisme : SFB1389-B01 - UNITE Glioblastoma
ID : Project ID 394046768

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Auteurs

Nirmeen Elmadany (N)

DKTK (German Cancer Consortium), Clinical Cooperation Unit (CCU), Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Department of Neurology, Medical Faculty Mannheim, MCTN, University of Heidelberg, 68167 Mannheim, Germany.

Obada T Alhalabi (OT)

Brain Tumor Translational Targets, DKFZ Junior Group, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Department of Neurosurgery, Heidelberg University Hospital, 69120 Heidelberg, Germany.

Michael Platten (M)

DKTK (German Cancer Consortium), Clinical Cooperation Unit (CCU), Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Department of Neurology, Medical Faculty Mannheim, MCTN, University of Heidelberg, 68167 Mannheim, Germany.
Immune Monitoring Unit, National Center for Tumor Diseases (NCT), 69120 Heidelberg, Germany.
Helmholtz Institute of Translational Oncology (HI-TRON), 55131 Mainz, Germany.
DKFZ Hector Cancer Institute, University Medical Center Mannheim, 68167 Mannheim, Germany.

Lukas Bunse (L)

DKTK (German Cancer Consortium), Clinical Cooperation Unit (CCU), Neuroimmunology and Brain Tumor Immunology, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Department of Neurology, Medical Faculty Mannheim, MCTN, University of Heidelberg, 68167 Mannheim, Germany.

Classifications MeSH