Control of B cell lymphoma recognition via natural killer inhibitory receptors implies a role for human Vγ9/Vδ2 T cells in tumor immunity

P Fisch, E Meuer, D Pende… - European Journal of …, 1997 - Wiley Online Library
P Fisch, E Meuer, D Pende, S Rothenfußer, O Viale, S Kock, S Ferrone, D Fradelizi, G Klein…
European Journal of Immunology, 1997Wiley Online Library
The Vγ9/Vδ2 T cell receptor (TCR) is expressed by most human γδ T cells. We show here
that cytotoxic T lymphocytes of the Vγ9/Vδ2 subset, but not of the Vδ1 subset of human γδ T
cells, express natural killer inhibitory receptors (KIR) with specificity for different HLA class I
alleles that down‐regulate TCR‐mediated signaling in response to HLA class I‐expressing
B cell lymphomas. Vγ9/Vδ2 T cell clones with a T helper cell phenotype lack KIR and
produce lymphokines in response to most human B cell lymphomas, just as they do upon …
Abstract
The Vγ9/Vδ2 T cell receptor (TCR) is expressed by most human γδ T cells. We show here that cytotoxic T lymphocytes of the Vγ9/Vδ2 subset, but not of the Vδ1 subset of human γδ T cells, express natural killer inhibitory receptors (KIR) with specificity for different HLA class I alleles that down‐regulate TCR‐mediated signaling in response to HLA class I‐expressing B cell lymphomas. Vγ9/Vδ2 T cell clones with a T helper cell phenotype lack KIR and produce lymphokines in response to most human B cell lymphomas, just as they do upon recognition of the HLA class l‐deficient human Burkitt's lymphoma Daudi. Thus, human Vγ9/Vδ2 T cells have an innate specificity for nonpolymorphic cell surface structures expressed by many lymphoma cells and their cytotoxic activity is controlled by KIR. These results imply a general role of human Vγ9/Vδ2 T cells in the defense against hematopoietic tumors that is distinct from NK cells.
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