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
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	  PMC
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			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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        Article: Journal article
    
 
    
        Document type
        Scientific Article
    
 
    
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        Language
        english
    
 
    
        Publication Year
        2005
    
 
    
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        0
    
 
    
    
        ISSN (print) / ISBN
        0027-8424
    
 
    
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        1091-6490
    
 
    
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	    Volume: 102,  
	    Issue: 5,  
	    Pages: 1351-1356 
	    Article Number: ,  
	    Supplement: ,  
	
    
 
    
        
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            Publisher
            National Academy of Sciences
        
 
        
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        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
    
 
    
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        Erfassungsdatum
        2005-09-09