Cutting edge:: Human γδ T cells are activated by intermediates of the 2-C-methyl-D-erythritol 4-phosphate pathway of isoprenoid biosynthesis

被引:72
|
作者
Altincicek, B
Moll, J
Campos, N
Foerster, G
Beck, E
Hoeffler, JF
Grosdemange-Billiard, C
Rodríguez-Concepción, M
Rohmer, M
Boronat, A
Eberl, M
Jomaa, H
机构
[1] Univ Giessen, Inst Biochem, D-35392 Giessen, Germany
[2] Joman Pharmaka GmbH, Giessen, Germany
[3] Univ Barcelona, Dept Bioquim & Biol Mol, Barcelona, Spain
[4] Univ Strasbourg, Inst Le Bel, CNRS, F-67070 Strasbourg, France
来源
JOURNAL OF IMMUNOLOGY | 2001年 / 166卷 / 06期
关键词
D O I
10.4049/jimmunol.166.6.3655
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Activation of V gamma9/V delta2 T cells by small nonprotein Ags is frequently observed after infection with various viruses, bacteria, and eukaryotic parasites. We suggested earlier that compounds synthesized by the 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway of isopentenyl pyrophosphate synthesis are responsible for the V gamma9/V delta2 T cell reactivity of many pathogens. Using genetically engineered Escherichia coli knockout strains, we now demonstrate that the ability of E. coli extracts to stimulate gamma delta T cell proliferation is abrogated when genes coding for essential enzymes of the MEP pathway, dxr or gcpE, are disrupted or deleted from the bacterial genome.
引用
收藏
页码:3655 / 3658
页数:4
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