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Authordc.contributor.authorChennamadhavuni, Divya 
Authordc.contributor.authorSaavedra-Avila, Noemi Alejandra 
Authordc.contributor.authorCarreño, Leandro J. 
Authordc.contributor.authorGuberman-Pfeffer, Matthew J. 
Authordc.contributor.authorArora, Pooja 
Authordc.contributor.authorYongqing, Tang 
Authordc.contributor.authorKoay, Hui Fern 
Authordc.contributor.authorGodfrey, Dale I. 
Authordc.contributor.authorKeshipeddy, Santosh 
Authordc.contributor.authorRichardson, Stewart K. 
Authordc.contributor.authorSundararaj, Srinivasan 
Authordc.contributor.authorLo, Jae Ho 
Authordc.contributor.authorWen, Xiangshu 
Authordc.contributor.author 
Admission datedc.date.accessioned2019-03-18T12:02:15Z
Available datedc.date.available2019-03-18T12:02:15Z
Publication datedc.date.issued2018
Cita de ítemdc.identifier.citationCell Chemical Biology, Volumen 25, Issue 5, 2018, Pages 571-584.e8
Identifierdc.identifier.issn24519448
Identifierdc.identifier.issn24519456
Identifierdc.identifier.other10.1016/j.chembiol.2018.02.009
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/167463
Abstractdc.description.abstract© 2018 Elsevier Ltd Glycosylceramides that activate CD1d-restricted invariant natural killer T (iNKT) cells have potential therapeutic applications for augmenting immune responses against cancer and infections. Previous studies using mouse models identified sphinganine variants of α-galactosylceramide as promising iNKT cell activators that stimulate cytokine responses with a strongly proinflammatory bias. However, the activities of sphinganine variants in mice have generally not translated well to studies of human iNKT cell responses. Here, we show that strongly proinflammatory and anti-tumor iNKT cell responses were achieved in mice by a variant of α-galactosylceramide that combines a sphinganine base with a hydrocinnamoyl ester on C6″ of the sugar. Importantly, the activities observed with this variant were largely preserved for human iNKT cell responses. Structural and in silico modeling studies provided a mechanistic basis for these findings and suggested basic principles for captu
Lenguagedc.language.isoen
Publisherdc.publisherElsevier Ltd
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceCell Chemical Biology
Keywordsdc.subjectcancer immunotherapy
Keywordsdc.subjectCD1d
Keywordsdc.subjectgalactosylceramide
Keywordsdc.subjectiNKT cells
Keywordsdc.subjectKRN7000
Keywordsdc.subjecttumor immunity
Keywordsdc.subjectα-GalCer
Títulodc.titleDual Modifications of α-Galactosylceramide Synergize to Promote Activation of Human Invariant Natural Killer T Cells and Stimulate Anti-tumor Immunity
Document typedc.typeArtículo de revista
dcterms.accessRightsdcterms.accessRightsAcceso Abierto
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile