PD-L1 in systemic immunity: unraveling its contribution to PD-1/PD-L1 blockade immunotherapy

dc.contributor.authorBocanegra Gondán, Ana Isabel
dc.contributor.authorBlanco, Ester
dc.contributor.authorFernández Hinojal, Gonzalo
dc.contributor.authorChocarro de Erauso, Luisa
dc.contributor.authorZuazo Ibarra, Miren
dc.contributor.departmentCiencias de la Saludes_ES
dc.contributor.departmentOsasun Zientziakeu
dc.contributor.funderGobierno de Navarra / Nafarroako Gobernuaes
dc.date.accessioned2021-02-04T12:24:47Z
dc.date.available2021-02-04T12:24:47Z
dc.date.issued2020
dc.description.abstractThe use of monoclonal antibodies targeting PD-1/PD-L1 axis completely changed anticancer treatment strategies. However, despite the significant improvement in overall survival and progression-free survival of patients undergoing these immunotherapy treatments, the only clinically accepted biomarker with some prediction capabilities for the outcome of the treatment is PD-L1 expression in tumor biopsies. Nevertheless, even when having PD-L1-positive tumors, numerous patients do not respond to these treatments. Considering the high cost of these therapies and the risk of immune-related adverse events during therapy, it is necessary to identify additional biomarkers that would facilitate stratifying patients in potential responders and non-responders before the start of immunotherapies. Here, we review the utility of PD-L1 expression not only in tumor cells but in immune system cells and their influence on the antitumor activity of immune cell subsets.en
dc.description.sponsorshipThe Oncoimmunology group is funded by Asociación Española Contra el Cáncer, (AECC PROYE16001ESCO); Instituto de Salud Carlos III, Spain, (FIS grant PI17/02119); and a 'Precipita' Crowdfunding grant (FECYT), no grant number; Government of Navarre grant (BMED 050-2019); Independent Clinical Research Projects Call (Instituto de Salud Carlos III, Spain; TRANSPOCART); Proyectos estratégicos I+D, Departamento de Industria, Gobierno de Navarra (DESCARTHES).en
dc.format.extent17 p.
dc.format.mimetypeapplication/pdfen
dc.identifier.doi10.3390/ijms21165918
dc.identifier.issn1422-0067 (Electronic)
dc.identifier.urihttps://academica-e.unavarra.es/handle/2454/39151
dc.language.isoengen
dc.publisherMDPIen
dc.relation.ispartofInternational Journal of Molecular Sciences, 2020, 21(16), 5918en
dc.relation.publisherversionhttps://doi.org/10.3390/ijms21165918
dc.rights© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.en
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectPD-L1en
dc.subjectImmunotherapyen
dc.subjectImmuneen
dc.subjectCheckpoint inhibitionen
dc.subjectSystemic myeloid subsetsen
dc.subjectLiquid biopsyen
dc.subjectBiomarkersen
dc.titlePD-L1 in systemic immunity: unraveling its contribution to PD-1/PD-L1 blockade immunotherapyen
dc.typeinfo:eu-repo/semantics/article
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dspace.entity.typePublication
relation.isAuthorOfPublicationfe5c362e-3c0c-4edb-aa2e-0de27c815ad2
relation.isAuthorOfPublication193d800d-c38c-4627-b9d8-d29435d8214c
relation.isAuthorOfPublication.latestForDiscoveryfe5c362e-3c0c-4edb-aa2e-0de27c815ad2

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