Modulation of histamine type II receptors on CD8+ T cells by interleukin-2 and cimetidine

Int Arch Allergy Immunol. 1992;97(1):8-16. doi: 10.1159/000236089.

Abstract

CD8+ T cells are known to play a major role in regulating immune functions under normal and disease conditions. In this study a radioligand binding assay was used to quantitate histamine type II (H2) receptors on activated T cells. The objective was to examine the expression of H2 receptors on T cells during activation with interleukin-2 (IL-2) and treatment with cimetidine. Activated suppressor T cells induced by concanavalin A+IL-2 showed a significant (p less than 0.01) increase in H2 receptors compared to the control nonactivated T cells. The T cells expressing the H2 receptors were identified as CD8+ cells; those among them that had an enhanced level of H2 receptors were identified as CD25+. Treatment of activated suppressor cells with the H2 receptor antagonist cimetidine at a concentration of 10(-5) M significantly reduced the number of H2 receptors. Suppressor cells induced by Con A+IL-2 were able to suppress both IgG and IgM production that was reversible with cimetidine. Incubation of lymphocytes with 50 U/ml IL-2 alone in 3-day culture significantly (p less than 0.005) enhanced H2 receptor expression. These studies demonstrate that activated suppressor T cells that are CD8+CD25+ have enhanced levels of H2 receptors and can be modulated by cimetidine.

Publication types

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

MeSH terms

  • Antibody Formation / drug effects
  • CD8 Antigens / analysis*
  • Cells, Cultured
  • Cimetidine / pharmacology*
  • Concanavalin A
  • Humans
  • Interleukin-2 / pharmacology*
  • Receptors, Histamine H2 / drug effects*
  • Receptors, Interleukin-2 / analysis
  • T-Lymphocyte Subsets / chemistry
  • T-Lymphocytes, Regulatory / chemistry
  • T-Lymphocytes, Regulatory / drug effects*

Substances

  • CD8 Antigens
  • Interleukin-2
  • Receptors, Histamine H2
  • Receptors, Interleukin-2
  • Concanavalin A
  • Cimetidine