Activation of human invariant natural killer T cells with a thioglycoside analogue of α-galactosylceramide

Copyright © 2011 Elsevier Inc. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 140(2011), 2 vom: 15. Aug., Seite 196-207
1. Verfasser: Hogan, Andrew E (VerfasserIn)
Weitere Verfasser: O'Reilly, Vincent, Dunne, Margaret R, Dere, Ravindra T, Zeng, Shijuan G, O'Brien, Cashel, Amu, Sylvie, Fallon, Padraic G, Exley, Mark A, O'Farrelly, Cliona, Zhu, Xiangming, Doherty, Derek G
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2011
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Antigens, CD1d Galactosylceramides Thiogalactosides Thioglycosides alpha-S-galactosylceramide alpha-galactosylceramide Interleukin-10 130068-27-8 mehr... Interleukin-12 187348-17-0 Interleukin-4 207137-56-2 Interferon-gamma 82115-62-6
Beschreibung
Zusammenfassung:Copyright © 2011 Elsevier Inc. All rights reserved.
Activation of CD1d-restricted invariant NKT (iNKT) cells with the glycolipid α-galactosylceramide (α-GalCer) confers protection against disease in murine models, however, clinical trials in humans have had limited impact. We synthesized a novel thioglycoside analogue of α-GalCer, denoted α-S-GalCer, and tested its efficacy for stimulating human iNKT cells in vitro. α-S-GalCer stimulated cytokine release by iNKT cells in a CD1d-dependent manner and primed CD1d(+) target cells for lysis. α-S-GalCer-stimulated iNKT cells induced maturation of monocyte-derived dendritic cells into antigen-presenting cells that released IL-12 and small amounts of IL-10. The nature and potency of α-S-GalCer and α-GalCer in human iNKT cell activation were similar. However, in contrast to α-GalCer, α-S-GalCer did not activate murine iNKT cells in vivo. Because of its enhanced stability in biological systems, α-S-GalCer may be superior to α-GalCer as a parent compound for developing adjuvant therapies for humans
Beschreibung:Date Completed 03.10.2011
Date Revised 25.07.2011
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-7035
DOI:10.1016/j.clim.2011.03.016