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The Journal of Immunology, 2005, 174: 6045-6053.
Copyright © 2005 by The American Association of Immunologists

{gamma}{delta} T Cells Respond Directly to Pathogen-Associated Molecular Patterns 1,2

Jodi F. Hedges, Kirk J. Lubick and Mark A. Jutila3

Veterinary Molecular Biology, Montana State University, Bozeman, MT 59718

{gamma}{delta} T cells recognize unprocessed or non-peptide Ags, respond rapidly to infection, and localize to mucosal surfaces. We have hypothesized that the innate functions of {gamma}{delta} T cells may be more similar to those of cells of the myeloid lineage than to other T cells. To begin to test this assumption, we have analyzed the direct response of cultured human and peripheral blood bovine {gamma}{delta} T cells to pathogen associated molecular patterns (PAMPs) in the absence of APCs using microarray, real-time RT-PCR, proteome array, and chemotaxis assays. Our results indicate that purified {gamma}{delta} T cells respond directly to PAMPs by increasing expression of chemokine and activation-related genes. The response was distinct from that to known {gamma}{delta} T cell Ags and different from the response of myeloid cells to PAMPs. In addition, we have analyzed the expression of a variety of PAMP receptors in {gamma}{delta} T cells. Freshly purified bovine {gamma}{delta} T cells responded more robustly to PAMPs than did cultured human cells and expressed measurable mRNA encoding a variety of PAMP receptors. Our results suggest that rapid response to PAMPs through the expression of PAMP receptors may be another innate role of {gamma}{delta} T cells.




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