Cutting Edge: Human γδ T Cells Are Activated by Intermediates of the 2-C-methyl-d -erythritol 4-phosphate Pathway of Isoprenoid Biosynthesis
Author(s) -
Boran Altincicek,
Jens M. Moll,
Narciso Campos,
G. Elizabeth Foerster,
Ewald Beck,
JeanFrançois Hoeffler,
Catherine GrosdemangeBilliard,
Manuel RodríguezConcepción,
Michel Rohmer,
Albert Boronat,
Matthias Eberl,
Hassan Jomaa
Publication year - 2001
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.166.6.3655
Subject(s) - isopentenyl pyrophosphate , escherichia coli , biosynthesis , enzyme , bacteria , biology , gene , biochemistry , cell , chemistry , microbiology and biotechnology , genetics
Activation of V gamma 9/V delta 2 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 gamma 9/V delta 2 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.
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