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Author | dc.contributor.author | Chennamadhavuni, Divya | |
Author | dc.contributor.author | Saavedra-Avila, Noemi Alejandra | |
Author | dc.contributor.author | Carreño, Leandro J. | |
Author | dc.contributor.author | Guberman-Pfeffer, Matthew J. | |
Author | dc.contributor.author | Arora, Pooja | |
Author | dc.contributor.author | Yongqing, Tang | |
Author | dc.contributor.author | Koay, Hui Fern | |
Author | dc.contributor.author | Godfrey, Dale I. | |
Author | dc.contributor.author | Keshipeddy, Santosh | |
Author | dc.contributor.author | Richardson, Stewart K. | |
Author | dc.contributor.author | Sundararaj, Srinivasan | |
Author | dc.contributor.author | Lo, Jae Ho | |
Author | dc.contributor.author | Wen, Xiangshu | |
Author | dc.contributor.author | | |
Admission date | dc.date.accessioned | 2019-03-18T12:02:15Z | |
Available date | dc.date.available | 2019-03-18T12:02:15Z | |
Publication date | dc.date.issued | 2018 | |
Cita de ítem | dc.identifier.citation | Cell Chemical Biology, Volumen 25, Issue 5, 2018, Pages 571-584.e8 | |
Identifier | dc.identifier.issn | 24519448 | |
Identifier | dc.identifier.issn | 24519456 | |
Identifier | dc.identifier.other | 10.1016/j.chembiol.2018.02.009 | |
Identifier | dc.identifier.uri | https://repositorio.uchile.cl/handle/2250/167463 | |
Abstract | dc.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 | |
Lenguage | dc.language.iso | en | |
Publisher | dc.publisher | Elsevier Ltd | |
Type of license | dc.rights | Attribution-NonCommercial-NoDerivs 3.0 Chile | |
Link to License | dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/cl/ | |
Source | dc.source | Cell Chemical Biology | |
Keywords | dc.subject | cancer immunotherapy | |
Keywords | dc.subject | CD1d | |
Keywords | dc.subject | galactosylceramide | |
Keywords | dc.subject | iNKT cells | |
Keywords | dc.subject | KRN7000 | |
Keywords | dc.subject | tumor immunity | |
Keywords | dc.subject | α-GalCer | |
Título | dc.title | Dual Modifications of α-Galactosylceramide Synergize to Promote Activation of Human Invariant Natural Killer T Cells and Stimulate Anti-tumor Immunity | |
Document type | dc.type | Artículo de revista | |
dcterms.accessRights | dcterms.accessRights | Acceso Abierto | |
Cataloguer | uchile.catalogador | SCOPUS | |
Indexation | uchile.index | Artículo de publicación SCOPUS | |
uchile.cosecha | uchile.cosecha | SI | |
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