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Wu, D.* ; Xing, G.W.* ; Poles, M.A.* ; Horowitz, A.* ; Kinjo, Y.* ; Sullivan, B.* ; Bodmer-Narkevitch, V.* ; Plettenburg, O.* ; Kronenberg, M.F.* ; Tsuji, M.* ; Ho, D.D.* ; Wong, C.H.*

Bacterial glycolipids and analogs as antigens for CD1d-restricted NKT cells.

Proc. Natl. Acad. Sci. U.S.A. 102, 1351-1356 (2005)
DOI PMC
Open Access Gold as soon as Publ. Version/Full Text is submitted to ZB.
The CD1 family of proteins binds self and foreign glycolipids for presentation to CD1-restricted T cells. To identify previously uncharacterized active CD1 ligands, especially those of microbial origin, numerous glycolipids were synthesized and tested for their ability to stimulate mouse and human natural killer T (NKT) cells. They included analogs of the well known NKT cell agonist alpha-galactosyl ceramide (alpha-GalCer), bacterial glycolipids, and variations of the self-glycolipid, sulfatide. Bacterial glycolipids, alpha-galacturonosyl-ceramides from Sphingomonas wittichii, although structurally similar to alpha-GalCer, have significant differences in the sugar head group as well as the ceramide portion. The Sphingomonas glycosphingolipids (GSLs) and sulfatide variants were shown to activate human NKT cells as measured by IL-4 and IFN-gamma secretion. Moreover, CD1d-dimer staining revealed human NKT cell reactivity toward these GSLs and to the sulfatides in a fashion comparable with alpha-GalCer. Because alpha-GalCer is a marine-sponge-derived ligand, our study here shows that bacterium-derived antigens are also able to stimulate mouse and human NKT cells.
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Publication type Article: Journal article
Document type Scientific Article
Language english
Publication Year 2005
HGF-reported in Year 0
ISSN (print) / ISBN 0027-8424
e-ISSN 1091-6490
Quellenangaben Volume: 102, Issue: 5, Pages: 1351-1356 Article Number: , Supplement: ,
Publisher National Academy of Sciences
Reviewing status Peer reviewed
Institute(s) Institute of Medicinal Chemistry (IMC)
POF-Topic(s) 30203 - Molecular Targets and Therapies
Research field(s) Enabling and Novel Technologies
PSP Element(s) G-506300-001
PubMed ID 15665086
Erfassungsdatum 2005-09-09