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dc.rights.licenseopenen_US
dc.contributor.authorHOFFMANN DAHL, Elin
dc.contributor.authorMBALA, Placide
hal.structure.identifierBordeaux population health [BPH]
hal.structure.identifierGlobal Health in the Global South [GHiGS]
dc.contributor.authorJUCHET, Sylvain
dc.contributor.authorTOURÉ, Abdoulaye
hal.structure.identifierBordeaux population health [BPH]
hal.structure.identifierGlobal Health in the Global South [GHiGS]
dc.contributor.authorMONTOYO, Alice
hal.structure.identifierBordeaux population health [BPH]
hal.structure.identifierGlobal Health in the Global South [GHiGS]
dc.contributor.authorSERRA, Beatrice
dc.contributor.authorKOJAN, Richard
dc.contributor.authorD'ORTENZIO, Eric
dc.contributor.authorBLOMBERG, Bjorn
dc.contributor.authorJASPARD, Marie
dc.date.accessioned2024-11-15T13:40:14Z
dc.date.available2024-11-15T13:40:14Z
dc.date.issued2024-10-01
dc.identifier.issn2214-109Xen_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/203312
dc.description.abstractEnEbola virus disease kills more than half of people infected. Since the disease is transmitted via close human contact, identifying individuals at the highest risk of developing the disease is possible on the basis of the type of contact (correlated with viral exposure). Different candidates for post-exposure prophylaxis (PEP; ie, vaccines, antivirals, and monoclonal antibodies) each have their specific benefits and limitations, which we discuss in this Viewpoint. Approved monoclonal antibodies have been found to reduce mortality in people with Ebola virus disease. As monoclonal antibodies act swiftly by directly targeting the virus, they are promising candidates for targeted PEP in contacts at high risk of developing disease. This intervention could save lives, halt viral transmission, and, ultimately, help curtail outbreak propagation. We explore how a strategic integration of monoclonal antibodies and vaccines as PEP could provide both immediate and long-term protection against Ebola virus disease, highlighting ongoing clinical research that aims to refine this approach, and discuss the transformative potential of a successful PEP strategy to help control viral haemorrhagic fever outbreaks.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.subject.enHemorrhagic Fever
dc.subject.enEbola
dc.subject.enHumans
dc.subject.enPost-Exposure Prophylaxis
dc.subject.enDisease Outbreaks
dc.subject.enEbola Vaccines
dc.subject.enAntibodies
dc.subject.enMonoclonal
dc.subject.enAntiviral Agents
dc.subject.enEbolavirus
dc.title.enImproving Ebola virus disease outbreak control through targeted post-exposure prophylaxis
dc.title.alternativeLancet Glob Healthen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/S2214-109X(24)00255-9en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed39270687en_US
bordeaux.journalThe Lancet global healthen_US
bordeaux.pagee1730-e1736en_US
bordeaux.volume12en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue10en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamGHIGS_BPHen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDInstitut de Recherche pour le Développementen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04785562
hal.version1
hal.date.transferred2024-11-15T13:40:16Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=The%20Lancet%20global%20health&rft.date=2024-10-01&rft.volume=12&rft.issue=10&rft.spage=e1730-e1736&rft.epage=e1730-e1736&rft.eissn=2214-109X&rft.issn=2214-109X&rft.au=HOFFMANN%20DAHL,%20Elin&MBALA,%20Placide&JUCHET,%20Sylvain&TOUR%C3%89,%20Abdoulaye&MONTOYO,%20Alice&rft.genre=article


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