Exogenous and endogenous glycolipid antigens activate NKT cells during microbial infections

被引:898
作者
Mattner, J
DeBord, KL
Ismail, N
Goff, RD
Cantu, C
Zhou, DP
Saint-Mezard, P
Wang, V
Gao, Y
Yin, N
Hoebe, K
Schneewind, O
Walker, D
Beutler, B
Teyton, L
Savage, PB [1 ]
Bendelac, A
机构
[1] Univ Chicago, Comm Immunol, Chicago, IL 60637 USA
[2] Univ Chicago, Comm Microbiol, Chicago, IL 60637 USA
[3] Univ Texas, Med Branch, Dept Pathol, Galveston, TX 77555 USA
[4] Brigham Young Univ, Dept Chem & Biochem, Provo, UT 84602 USA
[5] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nature03408
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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(1,2). 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.
引用
收藏
页码:525 / 529
页数:5
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