Diacylated sulfoglycolipids are novel mycobacterial antigens stimulating CD1-restricted T cells during infection with Mycobacterium tuberculosis

被引:225
作者
Gilleron, M
Stenger, S
Mazorra, Z
Wittke, F
Mariotti, S
Böhmer, G
Prandi, J
Mori, L
Puzo, G
De Libero, G
机构
[1] Univ Basel Hosp, Dept Res, CH-4031 Basel, Switzerland
[2] CNRS, Inst Pharmacol & Biol Struct, Dept Mecanismes Mol Infect Mycobacteriennes, F-31077 Toulouse, France
[3] Inst Klin Mikrobiol Immunol & Hyg, D-91054 Erlangen, Germany
[4] Bezirksklinikum Obermain, D-96248 Kutzenberg, Ebensfeld, Germany
关键词
vaccination; intracellular bacteria; protection; cytotoxic CD8(+) T cells; lipids;
D O I
10.1084/jem.20031097
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mycobacterial lipids comprise a heterogeneous group of molecules capable of inducing T cell responses in humans. To identify novel antigenic lipids and increase our understanding of lipid-mediated immune responses, we established a panel of T cell clones with different lipid specificities. Using this approach we characterized a novel lipid antigen belonging to the group of diacylated sulfoglycolipids purified from Mycobacterium tuberculosis. The structure of this sulfoglycolipid was identified as 2-palinitoyl or 2-stearoyl-3-hydroxyphthioceranoyl-2'-sulfate-alpha-alpha'-D-trehalose (Ac(2)SGL). Its immunogenicity is dependent on the presence of the sulfate group and of the two fatty acids. Ac(2)SGL is mainly presented by CD1b molecules after internalization in a cellular compartment with low pH. Ac(2)SGL-specific T cells release interferon gamma, efficiently recognize M. tuberculosis-infected cells, and kill intracellular bacteria. The presence of Ac(2)SGL-responsive T cells in vivo is strictly dependent on previous contact with M. tuberculosis, but independent from the development of clinically overt disease. These properties identify Ac(2)SGL as a promising candidate to be tested in novel vaccines against tuberculosis.
引用
收藏
页码:649 / 659
页数:11
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