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Oncolytic adenovirus and gene therapy with EphA2-BiTE for the treatment of pediatric high-grade gliomas.
- Source :
-
Journal for immunotherapy of cancer [J Immunother Cancer] 2021 May; Vol. 9 (5). - Publication Year :
- 2021
-
Abstract
- Background: Pediatric high-grade gliomas (pHGGs) are among the most common and incurable malignant neoplasms of childhood. Despite aggressive, multimodal treatment, the outcome of children with high-grade gliomas has not significantly improved over the past decades, prompting the development of innovative approaches.<br />Methods: To develop an effective treatment, we aimed at improving the suboptimal antitumor efficacy of oncolytic adenoviruses (OAs) by testing the combination with a gene-therapy approach using a bispecific T-cell engager (BiTE) directed towards the erythropoietin-producing human hepatocellular carcinoma A2 receptor (EphA2), conveyed by a replication-incompetent adenoviral vector (EphA2 adenovirus (EAd)). The combinatorial approach was tested in vitro, in vivo and thoroughly characterized at a molecular level.<br />Results: After confirming the relevance of EphA2 as target in pHGGs, documenting a significant correlation with worse clinical outcome of the patients, we showed that the proposed strategy provides significant EphA2-BiTE amplification and enhanced tumor cell apoptosis, on coculture with T cells. Moreover, T-cell activation through an agonistic anti-CD28 antibody further increased the activation/proliferation profiles and functional response against infected tumor cells, inducing eradication of highly resistant, primary pHGG cells. The gene-expression analysis of tumor cells and T cells, after coculture, revealed the importance of both EphA2-BiTE and costimulation in the proposed system. These in vitro observations translated into significant tumor control in vivo, in both subcutaneous and a more challenging orthotopic model.<br />Conclusions: The combination of OA and EphA2-BiTE gene therapy strongly enhances the antitumor activity of OA, inducing the eradication of highly resistant tumor cells, thus supporting the clinical translation of the approach.<br />Competing Interests: Competing interests: None declared.<br /> (© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.)
- Subjects :
- Adenoviridae metabolism
Adenoviridae pathogenicity
Animals
Antibodies, Bispecific metabolism
Apoptosis
Brain Neoplasms genetics
Brain Neoplasms metabolism
Brain Neoplasms virology
Cell Line, Tumor
Coculture Techniques
Cytotoxicity, Immunologic
Female
Gene Expression Regulation, Neoplastic
Genetic Vectors
Glioma genetics
Glioma metabolism
Glioma virology
Humans
Lymphocyte Activation
Lymphocytes, Tumor-Infiltrating immunology
Lymphocytes, Tumor-Infiltrating metabolism
Mice, Inbred NOD
Mice, SCID
Neoplasm Grading
Oncolytic Viruses metabolism
Oncolytic Viruses pathogenicity
Receptor, EphA2 metabolism
T-Lymphocytes immunology
T-Lymphocytes metabolism
Xenograft Model Antitumor Assays
Mice
Adenoviridae genetics
Antibodies, Bispecific genetics
Brain Neoplasms therapy
Genetic Therapy
Glioma therapy
Oncolytic Virotherapy
Oncolytic Viruses genetics
Receptor, EphA2 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2051-1426
- Volume :
- 9
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Journal for immunotherapy of cancer
- Publication Type :
- Academic Journal
- Accession number :
- 33963009
- Full Text :
- https://doi.org/10.1136/jitc-2020-001930