Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/100013
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dc.contributorDepartment of Health Technology and Informatics-
dc.creatorLiu, Z-
dc.creatorZhou, J-
dc.creatorYang, X-
dc.creatorLiu, Y-
dc.creatorZou, C-
dc.creatorLv, W-
dc.creatorChen, C-
dc.creatorCheng, KKY-
dc.creatorChen, T-
dc.creatorChang, LJ-
dc.creatorWu, D-
dc.creatorMao, J-
dc.date.accessioned2023-07-28T03:36:42Z-
dc.date.available2023-07-28T03:36:42Z-
dc.identifier.urihttp://hdl.handle.net/10397/100013-
dc.language.isoenen_US
dc.publisherBioMed Central Ltd.en_US
dc.rights© The Author(s). 2023. Open access. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.en_US
dc.rightsThe following publication Liu, Z., Zhou, J., Yang, X. et al. Safety and antitumor activity of GD2-Specific 4SCAR-T cells in patients with glioblastoma. Mol Cancer 22, 3 (2023) is available at https://doi.org/10.1186/s12943-022-01711-9.en_US
dc.subjectGD2en_US
dc.subject4SCAR‑Ten_US
dc.subjectGBMen_US
dc.subjectSafetyen_US
dc.subjectTumor microenvironmenten_US
dc.titleSafety and antitumor activity of GD2-Specific 4SCAR-T cells in patients with glioblastomaen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume22-
dc.identifier.doi10.1186/s12943-022-01711-9-
dcterms.abstractBackground: This study aimed to validate whether infusion of GD2-specific fourth-generation safety-designed chimeric antigen receptor (4SCAR)-T cells is safe and whether CAR-T cells exert anti-glioblastoma (GBM) activity.-
dcterms.abstractMethods: A total of eight patients with GD2-positive GBM were enrolled and infused with autologous GD2-specific 4SCAR-T cells, either through intravenous administration alone or intravenous combined with intracavitary administration.-
dcterms.abstractResults: 4SCAR-T cells expanded for 1–3 weeks and persisted at a low frequency in peripheral blood. Of the eight evaluable patients, four showed a partial response for 3 to 24 months, three had progressive disease for 6 to 23 months, and one had stable disease for 4 months after infusion. For the entire cohort, the median overall survival was 10 months from the infusion. GD2 antigen loss and infiltrated T cells were observed in the tumor resected after infusion.-
dcterms.abstractConclusion: Both single and combined infusions of GD2-specific 4SCAR-T cells in targeting GBM were safe and well tolerated, with no severe adverse events. In addition, GD2-specific 4SCAR-T cells partially mediate antigen loss and activate immune responses in the tumor microenvironment. Validation of our findings in a larger prospective trial is warranted.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationMolecular cancer, 2023, v. 22, 3-
dcterms.isPartOfMolecular cancer-
dcterms.issued2023-
dc.identifier.scopus2-s2.0-85145911702-
dc.identifier.pmid36617554-
dc.identifier.eissn1476-4598-
dc.identifier.artn3-
dc.description.validate202307 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera2336en_US
dc.identifier.SubFormID47533en_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China; Shenzhen Basic Research Program of Shenzhen Science and Technology Innovation Commissionen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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