Advancements and challenges in developing in vivo CAR T cell therapies for cancer treatment.
- Publisher:
- ELSEVIER
- Publication Type:
- Journal Article
- Citation:
- EBioMedicine, 2024, 106, pp. 105266
- Issue Date:
- 2024-08
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Bui, TA | |
dc.contributor.author | Mei, H | |
dc.contributor.author | Sang, R | |
dc.contributor.author | Ortega, DG | |
dc.contributor.author |
Deng, W |
|
dc.date.accessioned | 2024-09-12T23:22:22Z | |
dc.date.available | 2024-07-22 | |
dc.date.available | 2024-09-12T23:22:22Z | |
dc.date.issued | 2024-08 | |
dc.identifier.citation | EBioMedicine, 2024, 106, pp. 105266 | |
dc.identifier.issn | 2352-3964 | |
dc.identifier.issn | 2352-3964 | |
dc.identifier.uri | http://hdl.handle.net/10453/180801 | |
dc.description.abstract | The Chimeric Antigen Receptor (CAR) T cell therapy has emerged as a ground-breaking immunotherapeutic approach in cancer treatment. To overcome the complexity and high manufacturing cost associated with current ex vivo CAR T cell therapy products, alternative strategies to produce CAR T cells directly in the body have been developed in recent years. These strategies involve the direct infusion of CAR genes via engineered nanocarriers or viral vectors to generate CAR T cells in situ. This review offers a comprehensive overview of recent advancements in the development of T cell-targeted CAR generation in situ. Additionally, it identifies the challenges associated with in vivo CAR T method and potential strategies to overcome these issues. | |
dc.format | Print-Electronic | |
dc.language | eng | |
dc.publisher | ELSEVIER | |
dc.relation | http://purl.org/au-research/grants/nhmrc/1181889 | |
dc.relation.ispartof | EBioMedicine | |
dc.relation.isbasedon | 10.1016/j.ebiom.2024.105266 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | 1103 Clinical Sciences, 1117 Public Health and Health Services | |
dc.subject.classification | 3202 Clinical sciences | |
dc.subject.classification | 4202 Epidemiology | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Neoplasms | |
dc.subject.mesh | Immunotherapy, Adoptive | |
dc.subject.mesh | Receptors, Chimeric Antigen | |
dc.subject.mesh | T-Lymphocytes | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Genetic Vectors | |
dc.subject.mesh | Receptors, Antigen, T-Cell | |
dc.subject.mesh | T-Lymphocytes | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Neoplasms | |
dc.subject.mesh | Receptors, Antigen, T-Cell | |
dc.subject.mesh | Immunotherapy, Adoptive | |
dc.subject.mesh | Genetic Vectors | |
dc.subject.mesh | Receptors, Chimeric Antigen | |
dc.title | Advancements and challenges in developing in vivo CAR T cell therapies for cancer treatment. | |
dc.type | Journal Article | |
utslib.citation.volume | 106 | |
utslib.location.activity | Netherlands | |
utslib.for | 1103 Clinical Sciences | |
utslib.for | 1117 Public Health and Health Services | |
pubs.organisational-group | University of Technology Sydney | |
pubs.organisational-group | University of Technology Sydney/Faculty of Engineering and Information Technology | |
pubs.organisational-group | University of Technology Sydney/Faculty of Engineering and Information Technology/School of Biomedical Engineering | |
utslib.copyright.status | open_access | * |
dc.rights.license | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND 4.0). To view a copy of this license, visit https://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.date.updated | 2024-09-12T23:22:20Z | |
dc.rights.holder | © 2024 The Author(s). | |
pubs.publication-status | Published | |
pubs.volume | 106 |
Abstract:
The Chimeric Antigen Receptor (CAR) T cell therapy has emerged as a ground-breaking immunotherapeutic approach in cancer treatment. To overcome the complexity and high manufacturing cost associated with current ex vivo CAR T cell therapy products, alternative strategies to produce CAR T cells directly in the body have been developed in recent years. These strategies involve the direct infusion of CAR genes via engineered nanocarriers or viral vectors to generate CAR T cells in situ. This review offers a comprehensive overview of recent advancements in the development of T cell-targeted CAR generation in situ. Additionally, it identifies the challenges associated with in vivo CAR T method and potential strategies to overcome these issues.
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