Expression and function of the natural cytotoxicity receptor NKp46 on circulating malignant CD4+ T lymphocytes of Sézary syndrome patients

J Invest Dermatol. 2011 Apr;131(4):969-76. doi: 10.1038/jid.2010.404. Epub 2010 Dec 30.

Abstract

The natural cytotoxicity receptors NKp30, NKp44, and NKp46 were identified as activating receptors mainly expressed by natural killer (NK) lymphocytes. In this study we show that peripheral blood malignant CD4(+) T lymphocytes from patients with Sézary syndrome, an aggressive form of cutaneous T-cell lymphoma, express NKp46 at their cell surface. Although NKp46 does not behave as an independent functional receptor, its engagement provides a strong inhibiting signal on the malignant T lymphocyte CD3-induced proliferation. We show that this inhibition is correlated with a decreased phosphorylation of the CD3ζ chain associated with NKp46 and/or the TCR/CD3 complexes. Our results reveal that in addition to KIR3DL2/CD158k expression, NKp46 could represent an additional marker on the circulating malignant T lymphocytes of Sézary patients, where it displays an as yet unreported function of inhibitory co-receptor able to interfere with the processes governing their CD3-dependent proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers, Tumor
  • CD3 Complex / metabolism
  • CD4-Positive T-Lymphocytes / physiology*
  • Cell Division / immunology
  • Flow Cytometry
  • Gene Expression / immunology
  • Humans
  • In Vitro Techniques
  • Natural Cytotoxicity Triggering Receptor 1 / genetics*
  • Natural Cytotoxicity Triggering Receptor 1 / metabolism*
  • Neoplastic Cells, Circulating / immunology
  • Receptors, KIR2DL2 / genetics
  • Receptors, KIR2DL2 / metabolism
  • Receptors, KIR3DL1 / genetics
  • Receptors, KIR3DL1 / metabolism
  • Sezary Syndrome* / immunology
  • Sezary Syndrome* / pathology
  • Sezary Syndrome* / physiopathology
  • Signal Transduction / immunology
  • Skin Neoplasms* / immunology
  • Skin Neoplasms* / pathology
  • Skin Neoplasms* / physiopathology

Substances

  • Biomarkers, Tumor
  • CD3 Complex
  • KIR2DL2 protein, human
  • KIR3DL1 protein, human
  • NCR1 protein, human
  • Natural Cytotoxicity Triggering Receptor 1
  • Receptors, KIR2DL2
  • Receptors, KIR3DL1