Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/9496
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dc.contributor.authorLiu, Zhanqien
dc.contributor.authorLee, Fook-Theanen
dc.contributor.authorHanai, Nobuoen
dc.contributor.authorSmyth, Fiona Een
dc.contributor.authorBurgess, Antony Wen
dc.contributor.authorOld, Lloyd Jen
dc.contributor.authorScott, Andrew Men
dc.date.accessioned2015-05-15T22:36:43Z
dc.date.available2015-05-15T22:36:43Z
dc.date.issued2002-10-07en
dc.identifier.citationCancer Immunity 2002; 2(): 13en
dc.identifier.govdoc12747758en
dc.identifier.otherPUBMEDen
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/9496en
dc.description.abstractThe chimeric KM871 monoclonal antibody targets the GD3 disialoganglioside antigen and is under investigation for its immunotherapeutic potential in melanoma. Preclinical and phase I studies have demonstrated the biodistribution and specific tumour targeting of KM871 to metastatic melanoma in vivo, with a long half-life and lack of immunogenicity making it an attractive candidate for further clinical trials. In vitro studies have demonstrated KM871 induces high levels of cytotoxicity in both antibody-dependent cellular-cytotoxicity (ADCC) and complement-dependent cytotoxicity (CDC) assays. In order to investigate the potential for cytokine upregulation of KM871-mediated ADCC, freshly isolated healthy donor PBMC effector cells were cultured in the presence or absence of the cytokines interleukin-2, interleukin-12 and granulocyte/macrophage-colony stimulating factor and the ADCC determined over a 10-day period. In the absence of these cytokines, ADCC activity of 1 micro g/ml KM871 on (51) Cr-labeled SK-MEL-28 target cells could not be detected after 72 hrs of culture of PBMC effector cells in media. In contrast, ADCC mediated by KM871 was significantly enhanced and maintained for the 10-day study period upon culturing PBMCs with media containing IL-2 and/or IL-12, but not with GM-CSF. FACS analysis of the effector cell population indicated CD3-/CD16+56+ NK cells were primarily responsible for the KM871-mediated ADCC activity and a direct correlation was observed between the percentage of NK cells and the level of cytotoxicity mediated by the PBMCs. Furthermore, ADCC was significantly reduced using NK-depleted PBMCs. These results suggest combining IL-2 or IL-12 with KM871 may enhance KM871 immune-mediated cell killing in patients with metastatic melanoma.en
dc.language.isoenen
dc.subject.otherAntibodies, Monoclonal.pharmacologyen
dc.subject.otherAntibody-Dependent Cell Cytotoxicity.drug effectsen
dc.subject.otherAntigens, CD3.analysisen
dc.subject.otherAntigens, CD56.analysisen
dc.subject.otherAntigens, CD8.analysisen
dc.subject.otherCytokines.pharmacologyen
dc.subject.otherFlow Cytometryen
dc.subject.otherGangliosides.immunologyen
dc.subject.otherGranulocyte-Macrophage Colony-Stimulating Factor.pharmacologyen
dc.subject.otherHumansen
dc.subject.otherInterleukin-12.pharmacologyen
dc.subject.otherInterleukin-2.pharmacologyen
dc.subject.otherKiller Cells, Natural.cytology.drug effects.immunologyen
dc.subject.otherLeukocytes, Mononuclear.cytology.drug effects.immunologyen
dc.subject.otherReceptors, IgG.analysisen
dc.subject.otherRecombinant Fusion Proteins.immunology.pharmacologyen
dc.subject.otherT-Lymphocytes.cytology.drug effects.immunologyen
dc.subject.otherTime Factorsen
dc.subject.otherTumor Cells, Cultureden
dc.titleCytokine enhancement of in vitro antibody-dependent cellular cytotoxicity mediated by chimeric anti-GD3 monoclonal antibody KM871.en
dc.typeJournal Articleen
dc.identifier.journaltitleCancer immunityen
dc.identifier.affiliationLudwig Institute for Cancer Research, Melbourne Tumour Biology Branch, Austin and Repatriation Medical Centre, Heidelberg, Victoria, 3084, Australiaen
dc.description.pages13en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/12747758en
dc.type.austinJournal Articleen
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairetypeJournal Article-
crisitem.author.deptMolecular Imaging and Therapy-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
Appears in Collections:Journal articles
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