Cross-talk between activated human NK cells and CD4+ T cells via OX40-OX40 ligand interactions

J Immunol. 2004 Sep 15;173(6):3716-24. doi: 10.4049/jimmunol.173.6.3716.

Abstract

It is important to understand which molecules are relevant for linking innate and adaptive immune cells. In this study, we show that OX40 ligand is selectively induced on IL-2, IL-12, or IL-15-activated human NK cells following stimulation through NKG2D, the low affinity receptor for IgG (CD16) or killer cell Ig-like receptor 2DS2. CD16-activated NK cells costimulate TCR-induced proliferation, and IFN-gamma produced by autologous CD4+ T cells and this process is dependent upon expression of OX40 ligand and B7 by the activated NK cells. These findings suggest a novel and unexpected link between the natural and specific immune responses, providing direct evidence for cross-talk between human CD4+ T cells and NK receptor-activated NK cells.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antigens, CD / physiology
  • Antigens, Surface
  • B7-1 Antigen / metabolism
  • B7-1 Antigen / physiology*
  • B7-2 Antigen
  • CD28 Antigens / metabolism
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / metabolism*
  • Cell Communication / immunology*
  • Cell Division / immunology
  • Cell Line, Tumor
  • Cytokines / blood
  • Cytokines / physiology
  • Humans
  • Killer Cells, Natural / immunology
  • Killer Cells, Natural / metabolism*
  • Ligands
  • Lymphocyte Activation / immunology*
  • Membrane Glycoproteins / physiology
  • Membrane Proteins
  • Oligonucleotide Array Sequence Analysis
  • Receptor Cross-Talk / immunology*
  • Receptors, Antigen, T-Cell / physiology
  • Receptors, Immunologic / blood
  • Receptors, Immunologic / physiology
  • Receptors, KIR
  • Receptors, OX40
  • Receptors, Tumor Necrosis Factor / metabolism
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / metabolism*
  • Tumor Necrosis Factor-alpha / physiology
  • Up-Regulation / immunology

Substances

  • Antigens, CD
  • Antigens, Surface
  • B7-1 Antigen
  • B7-2 Antigen
  • CD28 Antigens
  • CD86 protein, human
  • Cytokines
  • Ligands
  • Membrane Glycoproteins
  • Membrane Proteins
  • Receptors, Antigen, T-Cell
  • Receptors, Immunologic
  • Receptors, KIR
  • Receptors, OX40
  • Receptors, Tumor Necrosis Factor
  • TNFRSF4 protein, human
  • Tumor Necrosis Factor-alpha