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Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11812
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dc.contributor.authorWoods, Katherineen
dc.contributor.authorCebon, Jonathan Sen
dc.date.accessioned2015-05-16T01:26:26Z
dc.date.available2015-05-16T01:26:26Z
dc.date.issued2013-07-17en
dc.identifier.citationClinical Cancer Research 2013; 19(15): 4021-3en
dc.identifier.govdoc23864163en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11812en
dc.description.abstractDespite success with immune checkpoint inhibitors, clinical benefit from cancer vaccines remains elusive. Combined targeting of melanoma-specific CD4(+) and CD8(+) T-lymphocyte epitopes was associated with improved survival compared with targeting either alone, or when a nonspecific helper epitope was used. We discuss the potential role of antigen-specific CD4 help.en
dc.language.isoenen
dc.subject.otherAntigens, CD4.immunologyen
dc.subject.otherCD4-Positive T-Lymphocytesen
dc.subject.otherCD8-Positive T-Lymphocytesen
dc.subject.otherCancer Vaccines.immunology.therapeutic useen
dc.subject.otherEpitopes, T-Lymphocyte.immunologyen
dc.subject.otherFlow Cytometryen
dc.subject.otherHumansen
dc.subject.otherImmunotherapyen
dc.subject.otherLymphocyte Activation.immunologyen
dc.subject.otherMelanoma.immunology.pathology.therapyen
dc.subject.otherSurvival Analysisen
dc.titleTumor-specific T-cell help is associated with improved survival in melanoma.en
dc.typeJournal Articleen
dc.identifier.journaltitleClinical Cancer Researchen
dc.identifier.affiliationLudwig Institute for Cancer Research Melbourne-Austin Branch, Heidelberg, Australiaen
dc.identifier.doi10.1158/1078-0432.CCR-13-1349en
dc.description.pages4021-3en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/23864163en
dc.type.austinJournal Articleen
local.name.researcherCebon, Jonathan S
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
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