CD28 is not directly involved in the response of human CD3- CD56+ natural killer cells to lipopolysaccharide: a role for T cells

Immunology. 2004 Apr;111(4):384-90. doi: 10.1111/j.0019-2805.2004.01834.x.

Abstract

We have previously shown that human CD3- CD56+ and CD3+ CD56+ cells from some individuals mount vigorous proliferative responses to lipopolysaccharide. Such responses have been blocked by the presence of cytotoxic T-lymphocyte antigen-4 immunoglobulin fusion protein in the cultures, implicating a role for B7-mediated costimulation. Here we confirm this inhibition of natural killer (NK) expansion using antibodies against B7-1 and B7-2. We were unable to specifically detect CD28 on the surface of resting or stimulated human peripheral blood NK cells, however, in either lipopolysaccharide-responsive or non-responsive individuals, using a panel of four different anti-CD28 monoclonal antibodies. T-cell depletion from peripheral blood mononuclear cell cultures resulted in a reduction in the induction of CD25 on activated CD3- CD56hi cells and in the expansion and proliferation of CD3- CD56+ NK cells. Furthermore, reconstitution experiments using peripheral blood dendritic cells and purified NK cells demonstrated that NK expansion could only be achieved in the presence of purified T cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antibodies, Monoclonal / immunology
  • Antigens, CD / immunology
  • B7-1 Antigen / immunology
  • B7-2 Antigen
  • CD28 Antigens / immunology*
  • CD3 Complex / blood
  • CD56 Antigen / blood*
  • Cell Communication / immunology
  • Cell Division / immunology
  • Cells, Cultured
  • Dendritic Cells / immunology
  • Humans
  • Killer Cells, Natural / immunology*
  • Lipopolysaccharides / immunology
  • Membrane Glycoproteins / immunology
  • Receptors, Interleukin-2 / blood
  • T-Lymphocytes / immunology*

Substances

  • Antibodies, Monoclonal
  • Antigens, CD
  • B7-1 Antigen
  • B7-2 Antigen
  • CD28 Antigens
  • CD3 Complex
  • CD56 Antigen
  • CD86 protein, human
  • Lipopolysaccharides
  • Membrane Glycoproteins
  • Receptors, Interleukin-2