Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/9729
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dc.contributor.authorMaraskovsky, Eugeneen
dc.contributor.authorSjölander, Sigriden
dc.contributor.authorDrane, Debbie Pen
dc.contributor.authorSchnurr, Maxen
dc.contributor.authorLe, Thuy T Ten
dc.contributor.authorMateo, Luisen
dc.contributor.authorLuft, Thomasen
dc.contributor.authorMasterman, Kelly-Anneen
dc.contributor.authorTai, Tsin-Yeeen
dc.contributor.authorChen, Qiyuanen
dc.contributor.authorGreen, Simonen
dc.contributor.authorSjölander, Andersen
dc.contributor.authorPearse, Martin Jen
dc.contributor.authorLemonnier, Francois Aen
dc.contributor.authorChen, Weisanen
dc.contributor.authorCebon, Jonathan Sen
dc.contributor.authorSuhrbier, Andreasen
dc.date.accessioned2015-05-15T22:55:46Z
dc.date.available2015-05-15T22:55:46Z
dc.date.issued2004-04-15en
dc.identifier.citationClinical Cancer Research; 10(8): 2879-90en
dc.identifier.govdoc15102697en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/9729en
dc.description.abstractNY-ESO-1 is a 180 amino-acid human tumor antigen expressed by many different tumor types and belongs to the family of "cancer-testis" antigens. In humans, NY-ESO-1 is one of the most immunogenic tumor antigens and NY-ESO-1 peptides have been shown to induce NY-ESO-1-specific CD8(+) CTLs capable of altering the natural course of NY-ESO-1-expressing tumors in cancer patients. Here we describe the preclinical immunogenicity and efficacy of NY-ESO-1 protein formulated with the ISCOMATRIX adjuvant (NY-ESO-1 vaccine). In vitro, the NY-ESO-1 vaccine was readily taken up by human monocyte-derived dendritic cells, and on maturation, these human monocyte-derived dendritic cells efficiently cross-presented HLA-A2-restricted epitopes to NY-ESO-1-specific CD8(+) T cells. In addition, epitopes of NY-ESO-1 protein were also presented on MHC class II molecules to NY-ESO-1-specific CD4(+) T cells. The NY-ESO-1 vaccine induced strong NY-ESO-1-specific IFN-gamma and IgG2a responses in C57BL/6 mice. Furthermore, the NY-ESO-1 vaccine induced NY-ESO-1-specific CD8(+) CTLs in HLA-A2 transgenic mice that were capable of lysing human HLA-A2(+) NY-ESO-1(+) tumor cells. Finally, C57BL/6 mice, immunized with the NY-ESO-1 vaccine, were protected against challenge with a B16 melanoma cell line expressing NY-ESO-1. These data illustrate that the NY-ESO-1 vaccine represents a potent therapeutic anticancer vaccine.en
dc.language.isoenen
dc.subject.otherAdjuvants, Immunologicen
dc.subject.otherAnimalsen
dc.subject.otherAntigens, CD4.biosynthesisen
dc.subject.otherAntigens, Neoplasm.chemistryen
dc.subject.otherAntineoplastic Agents.pharmacologyen
dc.subject.otherCD8-Positive T-Lymphocytes.immunology.metabolismen
dc.subject.otherCancer Vaccinesen
dc.subject.otherCell Line, Tumoren
dc.subject.otherDisease Progressionen
dc.subject.otherDose-Response Relationship, Drugen
dc.subject.otherEnzyme-Linked Immunosorbent Assayen
dc.subject.otherEpitopes.chemistryen
dc.subject.otherEscherichia coli.metabolismen
dc.subject.otherHLA-A2 Antigen.chemistryen
dc.subject.otherImmunity, Cellularen
dc.subject.otherImmunoglobulin G.chemistryen
dc.subject.otherImmunohistochemistryen
dc.subject.otherMelanoma, Experimentalen
dc.subject.otherMembrane Proteins.chemistryen
dc.subject.otherMiceen
dc.subject.otherMice, Inbred BALB Cen
dc.subject.otherMice, Inbred C57BLen
dc.subject.otherMice, Transgenicen
dc.subject.otherMonocytes.metabolismen
dc.subject.otherPeptides.chemistryen
dc.subject.otherPhenotypeen
dc.subject.otherPlasmids.metabolismen
dc.subject.otherRNA, Messenger.metabolismen
dc.subject.otherRecombinant Proteins.chemistryen
dc.subject.otherReverse Transcriptase Polymerase Chain Reactionen
dc.subject.otherTime Factorsen
dc.subject.otherTransfectionen
dc.titleNY-ESO-1 protein formulated in ISCOMATRIX adjuvant is a potent anticancer vaccine inducing both humoral and CD8+ t-cell-mediated immunity and protection against NY-ESO-1+ tumors.en
dc.typeJournal Articleen
dc.identifier.journaltitleClinical Cancer Researchen
dc.identifier.affiliationLudwig Institute for Cancer Research, Austin and Repatriation Medical Centre, Melbourne, Victoria, Australiaen
dc.description.pages2879-90en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/15102697en
dc.type.austinJournal Articleen
local.name.researcherCebon, Jonathan S
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
Appears in Collections:Journal articles
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