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Dual antigenic recognition by cloned human gamma delta T cells.
J Holoshitz, … , D R McKinley, N K Bayne
J Holoshitz, … , D R McKinley, N K Bayne
Published January 1, 1992
Citation Information: J Clin Invest. 1992;89(1):308-314. https://doi.org/10.1172/JCI115577.
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Research Article

Dual antigenic recognition by cloned human gamma delta T cells.

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Abstract

The function of gamma delta T cells is still elusive. The nature of the antigens that they recognize and the mode of presentation of these antigens are largely unknown. The majority of human peripheral gamma delta T cells bear a V gamma 9/V delta 2 T cell receptor, and display nonclonal reactivity to mycobacteria, without restriction by MHC. It is unknown whether these cells have clonal antigenic specificity as well. Here we describe rheumatoid arthritis-derived V gamma 9/V delta 2 T cell clones, displaying dual antigenic recognition: a nonclonal, MHC-unrestricted recognition of mycobacteria, and a clonal recognition of a short tetanus toxin peptide presented by HLA-DRw53, a nonpolymorphic class II MHC molecule associated with susceptibility to rheumatoid arthritis. This is the first evidence that V gamma 9/V delta 2 T cells can recognize nominal antigenic peptides presented by class II MHC molecules. These results suggest that much like alpha beta T cells, V gamma 9/V delta 2 cells may contribute to the immune response against foreign antigens in an antigen-specific and MHC-restricted manner. The reactivity of these gamma delta T cells to mycobacteria may represent a superantigen-like phenomenon.

Authors

J Holoshitz, L M Vila, B J Keroack, D R McKinley, N K Bayne

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