| Atincicek, B., Moll, J., Campos, N., Foerster, G., Beck, E., Hoeffler, J. F., Grosdemange-Billiard, C., Rodriguez-Concepcion, M., Rohmer, M., Boronat, A., Eberl, Matthias  ORCID: https://orcid.org/0000-0002-9390-5348 and Jomaa, H.
      2001.
      
      Cutting edge: human gamma delta T cells are activated by intermediates of the 2-C-methyl-D-erythritol 4-phosphate pathway of isoprenoid biosynthesis.
      The Journal of Immunology
      166
      
        (6)
      
      , pp. 3655-3658.
      
      10.4049/jimmunol.166.6.3655 | 
Abstract
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.
| Item Type: | Article | 
|---|---|
| Date Type: | Publication | 
| Status: | Published | 
| Schools: | Schools > Medicine Research Institutes & Centres > Systems Immunity Research Institute (SIURI) | 
| Subjects: | R Medicine > R Medicine (General) R Medicine > RZ Other systems of medicine | 
| Publisher: | American Association of Immunologists | 
| ISSN: | 0022-1767 | 
| Last Modified: | 27 Oct 2022 09:01 | 
| URI: | https://orca.cardiff.ac.uk/id/eprint/64137 | 
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