Journal
EUROPEAN JOURNAL OF IMMUNOLOGY
Volume 44, Issue 9, Pages 2571-2576Publisher
WILEY-BLACKWELL
DOI: 10.1002/eji.201444712
Keywords
Antigen presentation/processing; Antigen receptors; gamma delta T cell; T cells; TCR
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Funding
- Interdiziplinares Zentrum fur Klinische Forschung (IZKF) [01KS9603]
- IZKF [Z-6]
- German Excellence Initiative to the Graduate School of Life Sciences
- University of Wurzburg
- DAAD-STIBET Doktorandenprogramm
- Wilhelm Sander-Stiftung [2013.907.1]
- Fonds der chemischen Industrie (Liebig Stipendium)
- State of Bavaria (Habilitanden-stipendium)
- DAAD-German academic exchange service
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Pyrophosphorylated metabolites of isoprenoid-biosynthesis (phosphoantigens, PAgs) activate V gamma 9V delta 2 T cells during infections and trigger antitumor activity. This activation depends on expression of butyrophilin 3 A1 (BTN3A1) by antigen-presenting cells. This report defines the minimal genetic requirements for activation of V gamma 9V delta 2 T cells by PAgs and mAb 20.1. We compared PAg-presentation by BTN3A1-transduced CHO hamster cells with that of CHO cells containing the complete human chromosome 6 (Chr6). BTN3A1 expression alone was sufficient for activation of V gamma 9V delta 2 T-cell receptor transductants by mAb 20.1., while activation by PAgs also required the presence of Chr6. We take this finding as evidence that gene(s) on Chr6 in addition to BTN3A1 are mandatory for PAg-mediated activation of V gamma 9V delta 2 T cells. This observation is important for the design of animal models for PAg-mediated immune responses and provokes speculations about the analogy between genes controlling PAg presentation and MHC-localized genes controlling peptide-antigen presentation.
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