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dc.rights.licenseopenen_US
dc.contributor.authorHAYDAY, Adrian
hal.structure.identifierImmunology from Concept and Experiments to Translation = Immunologie Conceptuelle, Expérimentale et Translationnelle [ImmunoConcept]
dc.contributor.authorDECHANET-MERVILLE, Julie
IDREF: 061667994
dc.contributor.authorROSSJOHN, Jamie
dc.contributor.authorSILVA-SANTOS, Bruno
dc.date.accessioned2024-10-25T08:50:47Z
dc.date.available2024-10-25T08:50:47Z
dc.date.issued2024-10-04
dc.identifier.issn0036-8075en_US
dc.identifier.urioai:crossref.org:10.1126/science.abq7248
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/202802
dc.description.abstractEnThe premise of cancer immunotherapy is that cancers are specifically visible to an immune system tolerized to healthy self. The promise of cancer immunotherapy is that immune effector mechanisms and immunological memory can jointly eradicate cancers and inoperable metastases and de facto vaccinate against recurrence. For some patients with hitherto incurable diseases, including metastatic melanoma, this promise is being realized by game-changing immunotherapies based on αβ T cells. Today’s challenges are to bring benefit to greater numbers of patients of diverse ethnicities, target more cancer types, and achieve a cure while incurring fewer adverse events. In meeting those challenges, specific benefits may be offered by γδ T cells, which compose a second T cell lineage with distinct recognition capabilities and functional traits that bridge innate and adaptive immunity. γδ T cell–based clinical trials, including off-the-shelf adoptive cell therapy and agonist antibodies, are yielding promising results, although identifiable problems remain. In addressing those problems, we advocate that immunotherapies be guided by the distinctive biology of γδ T cells, as elucidated by ongoing research.
dc.language.isoENen_US
dc.sourcecrossref
dc.titleCancer immunotherapy by γδ T cells
dc.typeArticle de revueen_US
dc.identifier.doi10.1126/science.abq7248en_US
dc.subject.halSciences du Vivant [q-bio]/Immunologieen_US
dc.identifier.pubmed39361750en_US
bordeaux.journalScienceen_US
bordeaux.volume386en_US
bordeaux.hal.laboratoriesImmunoConcEpT - UMR 5164en_US
bordeaux.issue6717en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcedissemin
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
workflow.import.sourcedissemin
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.title=Cancer%20immunotherapy%20by%20%CE%B3%CE%B4%20T%20cells&rft.atitle=Cancer%20immunotherapy%20by%20%CE%B3%CE%B4%20T%20cells&rft.jtitle=Science&rft.date=2024-10-04&rft.volume=386&rft.issue=6717&rft.eissn=0036-8075&rft.issn=0036-8075&rft.au=HAYDAY,%20Adrian&DECHANET-MERVILLE,%20Julie&ROSSJOHN,%20Jamie&SILVA-SANTOS,%20Bruno&rft.genre=article


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