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dc.contributor.authorKlampatsa, A
dc.contributor.authorDimou, V
dc.contributor.authorAlbelda, SM
dc.date.accessioned2021-01-28T15:38:04Z
dc.date.available2021-01-28T15:38:04Z
dc.date.issued2021-04-03
dc.identifier.citationExpert opinion on biological therapy, 2020, pp. 1 - 14
dc.identifier.issn1471-2598
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4329
dc.identifier.eissn1744-7682
dc.identifier.doi10.1080/14712598.2021.1843628
dc.description.abstractIntroduction: Mesothelin (MSLN) is a tumor differentiation antigen normally restricted to the body's mesothelial surfaces, but significantly overexpressed in a broad range of solid tumors. For this reason, MSLN has emerged as an important target for the development of novel immunotherapies. This review focuses on anti-MSLN chimeric antigen receptor (CAR) T cell immunotherapy approaches.Areas covered: A brief overview of MSLN as a therapeutic target and existing anti-MSLN antibody-based drugs and vaccines is provided. A detailed account of anti-MSLN CAR-T cell approaches utilized in preclinical models is presented. Finally, a comprehensive summary of currently ongoing and completed anti-MSLN CAR-T cell clinical trials is discussed.Expert opinion: Initial trials using anti-MSLN CAR-T cells have been safe, but efficacy has been limited. Employing regional routes of delivery, introducing novel modifications leading to enhanced tumor infiltration and persistence, and improved safety profiles and combining anti-MSLN CAR-T cells with standard therapies, could render them more efficacious in the treatment of solid malignancies.
dc.formatPrint-Electronic
dc.format.extent1 - 14
dc.languageeng
dc.language.isoeng
dc.publisherTAYLOR & FRANCIS LTD
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.titleMesothelin-targeted CAR-T cell therapy for solid tumors.
dc.typeJournal Article
dcterms.dateAccepted2020-10-26
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1080/14712598.2021.1843628
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2020-11-12
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfExpert opinion on biological therapy
pubs.notesNot known
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
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.publication-statusPublished
pubs.embargo.termsNot known
icr.researchteamThoracic Oncology Immunotherapy Group (TOIG)
icr.researchteamThoracic Oncology Immunotherapy Group (TOIG)
dc.contributor.icrauthorKlampatsa, Astero


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