Enhancement of natural killer activity by an antibody to CD44

J Immunol. 1993 Feb 1;150(3):812-20.

Abstract

In this study, we examined the in vitro effect of an anti-CD44 mAb, S5, on NK function using canine PBMC as effectors. S5 enhanced NK activity in a dose-dependent and rapid fashion as did IM7, another anti-CD44 mAb that recognizes a common epitope(s) on CD44. Other anti-CD44 mAb (Hermes-1 and S3) that recognize epitopes distinct from S5 and IM7 had a variable effect on NK activity. The activation of increased killing by S5 only occurred when NK-sensitive targets were used, suggesting that lymphokine-activated killer cells were not being induced. Antibody-dependent cell cytotoxicity was not the mechanism involved in the augmentation of NK activity, nor was it Fc receptor-dependent, inasmuch as S5 F(ab')2 was able to increase NK activity. F(ab') fragments of S5 were equivalent to intact S5 in their ability to stimulate NK activity, demonstrating that cross-linking of CD44 was not a necessary component of stimulation, and that nonspecific agglutination of target and effector cells was not occurring via the two F(ab) arms. The enhancement of NK function was monocyte-independent and mediated by radioresistant cells, indicating that the antibody enhanced NK cells directly. This finding would suggest that CD44 can direct a transmembrane signal for NK cell activation.

Publication types

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

MeSH terms

  • Animals
  • Antibodies, Monoclonal / immunology*
  • Antibody-Dependent Cell Cytotoxicity
  • Cell Line
  • Dogs
  • Humans
  • Immunoglobulin Fab Fragments / immunology
  • Killer Cells, Natural / immunology*
  • Lymphocyte Activation
  • Mice
  • Monocytes / physiology
  • Receptors, Lymphocyte Homing / immunology*

Substances

  • Antibodies, Monoclonal
  • Immunoglobulin Fab Fragments
  • Receptors, Lymphocyte Homing