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Monoclonal antibodies that identify the CD3 molecules expressed specifically at the surface of porcine γδ‐T cells
Author(s) -
Yang Huaizhi,
Parkhouse R. Michael E.,
Wileman Thomas
Publication year - 2005
Publication title -
immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.297
H-Index - 133
eISSN - 1365-2567
pISSN - 0019-2805
DOI - 10.1111/j.1365-2567.2005.02137.x
Subject(s) - cd3 , t cell receptor , monoclonal antibody , epitope , antigen , biology , antigenicity , t cell , microbiology and biotechnology , antibody , immunoprecipitation , signal transduction , immunology , immune system , cd8
Summary The CD3 antigen is a surface structure associated with the T‐cell receptor (TCR) to form a complex involved in antigen recognition and signal transduction. Reports on the structures of the CD3 molecules associated with αβ‐ and γδ‐TCR have been contradictory. To investigate this issue, we raised a panel of monoclonal antibodies (mAb) against purified porcine CD3 molecules. Unlike the conventional anti‐CD3, these mAb reacted specifically with peripheral γδ‐T cells, but not with αβ‐T cells. Immunoprecipitation showed that the antibody recognized a subset of CD3 molecules that were associated with γδ‐TCR. Also unlike the conventional anti‐CD3, these mAb, though directed at two different epitope groups, failed to induce antigenic modulation, T‐cell proliferation and CD3‐redirected cytotoxicity. Taken together, these results suggest that there are differences in the antigenicity, signal transduction potentials and probably structural differences between the CD3 molecules expressed at the surface of αβ‐ and γδ‐T cells.