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

  • Paul Fisch
  • , Eva Meuer
  • , Daniela Pende
  • , Simon Rothenfußer
  • , Oriane Viale
  • , Sylvia Kock
  • , Soldano Ferrone
  • , Didier Fradelizi
  • , George Klein
  • , Lorenzo Moretta
  • , Hans Georg Rammensee
  • , Thierry Boon
  • , Pierre Coulie
  • , Pierre Van Der Bruggen

Research output: Contribution to journalArticlepeer-review

122 Scopus citations

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 I-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.

Original languageEnglish
Pages (from-to)3368-3379
Number of pages12
JournalEuropean Journal of Immunology
Volume27
Issue number12
DOIs
StatePublished - Dec 1997
Externally publishedYes

Keywords

  • B cell lymphoma
  • Natural killer receptor
  • γδ T lymphocyte

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