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dc.contributor.authorMILLS, KINGSTONen
dc.date.accessioned2016-06-23T12:33:23Z
dc.date.available2016-06-23T12:33:23Z
dc.date.issued2015en
dc.date.submitted2015en
dc.identifier.citationBrummelman J, Wilk MM, Han WG, van Els CA, Mills KH, Roads to the development of improved pertussis vaccines paved by immunology., Pathogens and disease, 73, 8, 2015, ftv067en
dc.identifier.issn2049-632Xen
dc.identifier.otherYen
dc.descriptionPUBLISHEDen
dc.description.abstractCurrent acellular pertussis vaccines have various shortcomings, which may contribute to their suboptimal efficacy and waning immunity in vaccinated populations. This calls for the development of new pertussis vaccines capable of inducing long-lived protective immunity. Immunization with whole cell pertussis vaccines and natural infection with Bordetella pertussis induce distinct and more protective immune responses when compared with immunization with acellular pertussis vaccines. Therefore, the immune responses induced with whole cell vaccine or after infection can be used as a benchmark for the development of third-generation vaccines against pertussis. Here, we review the literature on the immunology of B. pertussis infection and vaccination and discuss the lessons learned that will help in the design of improved pertussis vaccines.en
dc.format.extentftv067en
dc.relation.ispartofseriesPathogens and diseaseen
dc.relation.ispartofseries73en
dc.relation.ispartofseries8en
dc.rightsYen
dc.subjectBordetella pertussisen
dc.subjectT cellen
dc.subjectToll-like receptor agonisten
dc.titleRoads to the development of improved pertussis vaccines paved by immunology.en
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/millsken
dc.identifier.rssinternalid107739en
dc.identifier.doihttp://dx.doi.org/10.1093/femspd/ftv067en
dc.rights.ecaccessrightsopenAccess
dc.subject.TCDThemeImmunology, Inflammation & Infectionen
dc.identifier.orcid_id0000-0003-3646-8222en
dc.identifier.urihttp://hdl.handle.net/2262/76635


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