CD56bright NK cells are enriched at inflammatory sites and can engage with monocytes in a reciprocal program of activation

J Immunol. 2004 Nov 15;173(10):6418-26. doi: 10.4049/jimmunol.173.10.6418.

Abstract

Human NK cells may be divided into a CD56(dim) subset and a CD56(bright) subset. In peripheral blood, CD56(dim) NK cells dominate, whereas in lymph nodes, CD56(bright) NK cells are more common. In this study we show that CD56(bright) NK cells accumulate within inflammatory lesions in a wide variety of clinical diseases affecting several different anatomical sites. We demonstrate that when activated by the monokines IL-12, IL-15, and IL-18, these NK cells promote TNF-alpha production by CD14(+) monocytes in a manner that is dependent on cell:cell contact. Conversely, CD14(+) monocytes synergize with monokines to promote IFN-gamma production by these NK cells. Again, this interaction is dependent on cell:cell contact. The experiments show that CD56(bright) NK cells accumulate in inflammatory lesions and, in the appropriate cytokine environment, can engage with CD14(+) monocytes in a reciprocal activatory fashion, thereby amplifying the inflammatory response. Such a positive feedback loop is likely to be important in the pathogenesis of chronic inflammatory conditions such as rheumatoid arthritis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arthritis, Rheumatoid / immunology
  • CD56 Antigen / biosynthesis*
  • Cell Aggregation / immunology
  • Cell Communication / immunology*
  • Cells, Cultured
  • Coculture Techniques
  • Cytokines / physiology
  • Humans
  • Immunophenotyping
  • Inflammation / immunology
  • Inflammation / metabolism
  • Interferon-gamma / biosynthesis
  • Killer Cells, Natural / immunology*
  • Killer Cells, Natural / metabolism
  • Killer Cells, Natural / pathology*
  • Lipopolysaccharide Receptors / biosynthesis
  • Lymphocyte Activation / immunology*
  • Lymphocyte Subsets / immunology
  • Lymphocyte Subsets / metabolism
  • Lymphocyte Subsets / pathology
  • Macrophage Activation / immunology*
  • Monocytes / immunology*
  • Monocytes / metabolism
  • Monocytes / pathology*
  • Organ Specificity / immunology

Substances

  • CD56 Antigen
  • Cytokines
  • Lipopolysaccharide Receptors
  • Interferon-gamma