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dc.rights.licenseopenen_US
hal.structure.identifierImmunology from Concept and Experiments to Translation = Immunologie Conceptuelle, Expérimentale et Translationnelle [ImmunoConcept]
dc.contributor.authorKHAIRALLAH, Camille
hal.structure.identifierImmunology from Concept and Experiments to Translation = Immunologie Conceptuelle, Expérimentale et Translationnelle [ImmunoConcept]
dc.contributor.authorNETZER, Sonia
hal.structure.identifierImmunology from Concept and Experiments to Translation = Immunologie Conceptuelle, Expérimentale et Translationnelle [ImmunoConcept]
dc.contributor.authorVILLACRECES, Arnaud
hal.structure.identifierImmunology from Concept and Experiments to Translation = Immunologie Conceptuelle, Expérimentale et Translationnelle [ImmunoConcept]
dc.contributor.authorJUZAN, Marina
dc.contributor.authorROUSSEAU, Benoît
dc.contributor.authorDULANTO, Sara
dc.contributor.authorGIESE, Alban
dc.contributor.authorCOSTET, Pierre
hal.structure.identifierImmunology from Concept and Experiments to Translation = Immunologie Conceptuelle, Expérimentale et Translationnelle [ImmunoConcept]
dc.contributor.authorPRALORAN, Vincent
hal.structure.identifierImmunology from Concept and Experiments to Translation = Immunologie Conceptuelle, Expérimentale et Translationnelle [ImmunoConcept]
dc.contributor.authorMOREAU, Jean-François
dc.contributor.authorDUBUS, Pierre
dc.contributor.authorVERMIJLEN, David
hal.structure.identifierImmunology from Concept and Experiments to Translation = Immunologie Conceptuelle, Expérimentale et Translationnelle [ImmunoConcept]
dc.contributor.authorDECHANET-MERVILLE, Julie
IDREF: 061667994
hal.structure.identifierImmunology from Concept and Experiments to Translation = Immunologie Conceptuelle, Expérimentale et Translationnelle [ImmunoConcept]
dc.contributor.authorCAPONE, Myriam
dc.date.accessioned2021-10-27T08:22:41Z
dc.date.available2021-10-27T08:22:41Z
dc.date.issued2015-03-01
dc.identifier.issn1553-7374en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/117094
dc.description.abstractEnCytomegalovirus (CMV) is a leading infectious cause of morbidity in immune-compromised patients. γδ T cells have been involved in the response to CMV but their role in protection has not been firmly established and their dependency on other lymphocytes has not been addressed. Using C57BL/6 αβ and/or γδ T cell-deficient mice, we here show that γδ T cells are as competent as αβ T cells to protect mice from CMV-induced death. γδ T cell-mediated protection involved control of viral load and prevented organ damage. γδ T cell recovery by bone marrow transplant or adoptive transfer experiments rescued CD3ε-/- mice from CMV-induced death confirming the protective antiviral role of γδ T cells. As observed in humans, different γδ T cell subsets were induced upon CMV challenge, which differentiated into effector memory cells. This response was observed in the liver and lungs and implicated both CD27+ and CD27- γδ T cells. NK cells were the largely preponderant producers of IFNγ and cytotoxic granules throughout the infection, suggesting that the protective role of γδ T cells did not principally rely on either of these two functions. Finally, γδ T cells were strikingly sufficient to fully protect Rag-/-γc-/- mice from death, demonstrating that they can act in the absence of B and NK cells. Altogether our results uncover an autonomous protective antiviral function of γδ T cells, and open new perspectives for the characterization of a non classical mode of action which should foster the design of new γδ T cell based therapies, especially useful in αβ T cell compromised patients.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enAnimals
dc.subject.enHerpesviridae Infections
dc.subject.enImmunity
dc.subject.enCellular
dc.subject.enMice
dc.subject.enMice
dc.subject.enKnockout
dc.subject.enMuromegalovirus
dc.subject.enReceptors
dc.subject.enAntigen
dc.subject.enT-Cell
dc.subject.engamma-delta
dc.subject.enT-Lymphocytes
dc.title.enγδ T cells confer protection against murine cytomegalovirus (MCMV).
dc.title.alternativePLoS Pathogen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1371/journal.ppat.1004702en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologie
dc.identifier.pubmed25747674en_US
bordeaux.journalPLoS Pathogensen_US
bordeaux.pagee1004702en_US
bordeaux.volume11en_US
bordeaux.hal.laboratoriesImmunoConcEpT - UMR 5164en_US
bordeaux.issue3en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-03760886
hal.version1
hal.exportfalse
workflow.import.sourcepubmed
dc.rights.ccCC BYen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=PLoS%20Pathogens&rft.date=2015-03-01&rft.volume=11&rft.issue=3&rft.spage=e1004702&rft.epage=e1004702&rft.eissn=1553-7374&rft.issn=1553-7374&rft.au=KHAIRALLAH,%20Camille&NETZER,%20Sonia&VILLACRECES,%20Arnaud&JUZAN,%20Marina&ROUSSEAU,%20Beno%C3%AEt&rft.genre=article


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