IL-2 protects against anti-CD3-induced cell death in human medullary thymocytes

J Immunol. 1990 Sep 1;145(5):1364-8.

Abstract

In recent years, several studies have confirmed the clonal elimination of thymocytes with receptors that recognize Ag and MHC molecules present on the membrane of thymic stromal cells, a process that may be relevant to the establishment of self-tolerance. In our work, we show that anti-CD3 treatment of single positive CD4+ or CD8+ human medullary thymocytes (obtained by anti-CD1a plus C) induces their apoptotic death. Some events commonly associated with the early steps of normal activation (IL-2R expression, increase in cytoplasmic Ca2+) are also induced after anti-CD3 treatment. Nevertheless, IL-2 is not secreted by these activated cells. The addition of exogenous IL-2 inhibits the apoptosis induced by anti-CD3. We suggest that the lack of secretion of IL-2 by medullary thymocytes may be a physiologic mechanism implicated in the process of negative selection that leads to tolerance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal
  • Antigens, Differentiation, T-Lymphocyte / analysis
  • Antigens, Differentiation, T-Lymphocyte / physiology*
  • CD3 Complex
  • CD4-Positive T-Lymphocytes / immunology
  • CD8 Antigens
  • Calcium / physiology
  • Cell Survival
  • Cytoplasm / metabolism
  • DNA / analysis
  • Humans
  • Immune Tolerance*
  • In Vitro Techniques
  • Interleukin-2 / pharmacology*
  • Lymphocyte Activation
  • Receptors, Antigen, T-Cell / physiology*
  • Receptors, Interleukin-2 / metabolism
  • Solubility
  • T-Lymphocytes / physiology*
  • Thymus Gland / cytology*

Substances

  • Antibodies, Monoclonal
  • Antigens, Differentiation, T-Lymphocyte
  • CD3 Complex
  • CD8 Antigens
  • Interleukin-2
  • Receptors, Antigen, T-Cell
  • Receptors, Interleukin-2
  • DNA
  • Calcium