Antigen presentation by T cells inhibits IL-2 production and induces IL-4 release due to altered cognate signals

J Immunol. 1996 Apr 15;156(8):2769-75.

Abstract

Conflicting results of the effects of Ag presentation by MHC class II-expressing T cells have been described. In some studies class II-expressing T cells have been shown to act as effective APCs, while others have reported that the recognition of Ag on the surface of another T cell inactivates IL-2 production. In this study we have investigated the mechanisms involved in Ag presentation by T cells. The results obtained suggest that 1) lack of costimulation is not responsible for the inhibitory effects of T cell Ag presentation on IL-2 production; the provision of costimulation by immobilized anti-CD28 Ab or by the addition of accessory cells failed to reverse the effects of T cell Ag presentation, but restored the response to immobilized anti-CD3; 2) T cell Ag presentation induced a minimal increase in intracellular Ca2+ compared with that induced by antigen-pulsed B cells; this difference in the calcium response is not explained by quantitative differences in ligand density between B cells and T cells; and 3) despite the weak calcium signal, T cell presentation supported IL-4 release in the absence of IL-2 production. Taken together these data suggest that T cell Ag presentation leads to altered TCR/CD3-transduced signals, which biases the T cell towards a Th2 phenotype.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigen Presentation* / drug effects
  • Antigen-Presenting Cells / drug effects
  • Antigen-Presenting Cells / immunology*
  • Antigen-Presenting Cells / metabolism
  • B-Lymphocytes / immunology
  • B-Lymphocytes / metabolism
  • Calcium / metabolism
  • Cell Line
  • Extracellular Space / metabolism
  • Humans
  • Interleukin-12 / pharmacology
  • Interleukin-2 / antagonists & inhibitors*
  • Interleukin-2 / biosynthesis*
  • Interleukin-2 / metabolism
  • Interleukin-4 / metabolism*
  • Lymphocyte Activation
  • Mice
  • Signal Transduction / immunology*
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism

Substances

  • Interleukin-2
  • Interleukin-12
  • Interleukin-4
  • Calcium