CD40 ligation inhibits IL-2 and SAC+IL-2 induced proliferation in chronic lymphocytic leukaemia cells

Scand J Immunol. 1997 Jun;45(6):706-14. doi: 10.1046/j.1365-3083.1997.d01-451.x.

Abstract

This paper reports on differences between B cell-type chronic lymphocytic leukaemia (B-CLL) and normal B cells in their response to IL-2+thioredoxin (Trx), Staphylococcus aureus Cowan strain 1 (SAC)+IL-2+Trx, and to CD40 ligation of IL-2+Trx and SAC+IL-2+Trx stimulation. The authors found that Trx acted synergistically with IL-2 and SAC+IL-2 in inducing DNA synthesis in B-CLL cells, but not in the normal B cells. Interestingly, IL-2+Trx alone was found to induce proliferation in B-CLL cells from patients with advanced stages of disease. In addition, we also found that IL-2+Trx and SAC+IL-2+Trx-induced DNA synthesis of B-CLL cells was inhibited by CD40 activation (by soluble anti-CD40 MoAb and anti-CD40 MoAb presented on irradiated CD32L cells). In clear contrast, SAC+IL-2+ Trx-induced DNA synthesis of normal B cells was not inhibited by soluble anti-CD40 MoAb. The authors therefore conclude that B-CLL cells differ from normal B cells in their response to IL-2 (IL-2+Trx) and CD40 ligation.

Publication types

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

MeSH terms

  • Adult
  • Antibodies, Monoclonal / pharmacology
  • B-Lymphocytes / drug effects
  • B-Lymphocytes / immunology
  • CD40 Antigens / immunology*
  • CD40 Antigens / metabolism*
  • CD40 Antigens / pharmacology
  • Cell Division / drug effects
  • Cell Division / immunology
  • DNA Replication / drug effects
  • Fetal Blood / immunology
  • Humans
  • Interleukin-2 / pharmacology*
  • Leukemia, Lymphocytic, Chronic, B-Cell / immunology*
  • Leukemia, Lymphocytic, Chronic, B-Cell / metabolism
  • Leukemia, Lymphocytic, Chronic, B-Cell / pathology
  • Lymphocyte Activation / drug effects*
  • Staphylococcus aureus / immunology*
  • T-Lymphocytes / immunology
  • Thioredoxins / pharmacology
  • Tumor Cells, Cultured

Substances

  • Antibodies, Monoclonal
  • CD40 Antigens
  • Interleukin-2
  • Thioredoxins