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dc.contributor.authorKlampatsa, A
dc.contributor.authorHaas, AR
dc.contributor.authorMoon, EK
dc.contributor.authorAlbelda, SM
dc.coverage.spatialSwitzerland
dc.date.accessioned2022-09-02T08:13:01Z
dc.date.available2022-09-02T08:13:01Z
dc.date.issued2017-09-01
dc.identifierARTN 115
dc.identifiercancers9090115
dc.identifier.citationCancers, 2017, 9 (9), pp. E115 -en_US
dc.identifier.issn2072-6694
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5372
dc.identifier.eissn2072-6694
dc.identifier.eissn2072-6694
dc.identifier.doi10.3390/cancers9090115
dc.description.abstractCancer immunotherapy has now become a recognized approach to treating cancers. In addition to checkpoint blockade, adoptive T cell transfer (ACT) using chimeric antigen receptors (CARs) has shown impressive clinical outcomes in leukemias and is now being explored in solid tumors. CARs are engineered receptors, stably or transiently transduced into T cells, that aim to enhance T cell effector function by recognizing and binding to a specific tumor-associated antigen. In this review, we provide a summary of CAR T cell preclinical studies and clinical trials for malignant pleural mesothelioma (MPM), a rare, locally invasive pleural cancer with poor prognosis. We list other attractive potential targets for CAR T cell therapy for MPM, and discuss augmentation strategies of CAR T cell therapy with other forms of immunotherapy in this disease.
dc.formatElectronic
dc.format.extentE115 -
dc.languageeng
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.relation.ispartofCancers
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectadoptive cell transfer
dc.subjectchimeric antigen receptor T cells
dc.subjectimmunotherapy
dc.subjectmesothelioma
dc.titleChimeric Antigen Receptor (CAR) T Cell Therapy for Malignant Pleural Mesothelioma (MPM).en_US
dc.typeJournal Article
dcterms.dateAccepted2017-08-30
dc.date.updated2022-09-02T08:12:26Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.3390/cancers9090115en_US
rioxxterms.licenseref.startdate2017-09-01
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/28862644
pubs.issue9
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics/Thoracic Oncology Immunotherapy Group (TOIG)
pubs.organisational-group/ICR/ImmNet
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.3390/cancers9090115
pubs.volume9
icr.researchteamThor Onco Immuno Groupen_US
dc.contributor.icrauthorKlampatsa, Astero
icr.provenanceDeposited by Mr Arek Surman on 2022-09-02. Deposit type is initial. No. of files: 1. Files: Chimeric Antigen Receptor (CAR) T Cell Therapy for Malignant Pleural Mesothelioma (MPM). .pdf


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