@article{cc1b99cc75df464497c436e6ae1df4ed,
title = "Exogenous and endogenous glycolipid antigens activate NKT cells during microbial infections",
abstract = "CD1d-restricted natural killer T (NKT) cells are innate-like lymphocytes that express a conserved T-cell receptor and contribute to host defence against various microbial pathogens. However, their target lipid antigens have remained elusive. Here we report evidence for microbial, antigen-specific activation of NKT cells against Gram-negative, lipopolysaccharide (LPS)-negative alpha-Proteobacteria such as Ehrlichia muris and Sphingomonas capsulata. We have identified glycosylceramides from the cell wall of Sphingomonas that serve as direct targets for mouse and human NKT cells, controlling both septic shock reaction and bacterial clearance in infected mice. In contrast, Gram-negative, LPS-positive Salmonella typhimurium activates NKT cells through the recognition of an endogenous lysosomal glycosphingolipid, iGb3, presented by LPS-activated dendritic cells. These findings identify two novel antigenic targets of NKT cells in antimicrobial defence, and show that glycosylceramides are an alternative to LPS for innate recognition of the Gram-negative, LPS-negative bacterial cell wall.",
author = "Jochen Mattner and DeBord, {Kristin L.} and Nahed Ismail and Goff, {Randal D.} and Carlos Cantu and Dapeng Zhou and Pierre Saint-Mezard and Vivien Wang and Ying Gao and Ning Yin and Kasper Hoebe and Olaf Schneewind and David Walker and Bruce Beutler and Luc Teyton and Savage, {Paul B.} and Albert Bendelac",
note = "Funding Information: Acknowledgements We thank K. J. L. Hammond for critical reading of the manuscript, and S. Sidobre, L. Sidobre, K. J. L. Hammond and A. Khurana for mCD1d protein. This work was supported by grants from the National Institutes of Health (to M.K., to C-H.W. and to M.T.). Y.K. was supported in part by the Yamada Science Foundation. Funding Information: Acknowledgements We thank D. Wei for reading the manuscript, K. Thompson for help with biochemical characterization of Sphingomonas and growth of bacteria, S. Porcelli for the gift of anti-human CD1d, R. Duggan, J. Marvin and B. Eisfelder for cell sorting, L. Taylor for managing the mouse colonies, and the University of Chicago Digestive Disease Research center for equipment. Supported by NIH grants to A.B., P.S.B. and L.T., an NIH award to K.L.D. and O.S., an NIH grant to B.B., a Cancer Research Institute fellowship to J.M. and D.Z., and a fellowship from the Fondation pour la Recherche Medicale to P.S.-M.",
year = "2005",
month = mar,
day = "24",
doi = "10.1038/nature03408",
language = "English (US)",
volume = "434",
pages = "525--529",
journal = "Nature",
issn = "0028-0836",
publisher = "Nature Publishing Group",
number = "7032",
}