Requirement of IL-7 for IL-4-producing potential of MHC class I-selected CD4-CD8-TCR alpha beta+ thymocytes

Int Immunol. 1997 Jan;9(1):73-9. doi: 10.1093/intimm/9.1.73.

Abstract

IL-7 plays an important role in the growth and differentiation of T cells. We have previously reported that IL-7 induces preferential expansion of MHC class I-selected CD4-CD8-TCR alpha beta+ thymocytes which express a skewed V beta repertoire and are potent IL-4 producers. In this report, we provide evidence that IL-1 in combination with granulocyte macrophage colony stimulating factor can also expand this population. Yet, these cells do not share the functional characteristics of those obtained in the presence of IL-7, i.e. cytotoxic activity and high IL-4 production. These functional capacities can be acquired by adding IL-7. In conclusion, our findings demonstrate that the capacity of MHC class I-selected CD4-CD8-TCR alpha beta+ thymocytes to produce IL-4 as well as to kill target cells is IL-7 dependent.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / pharmacology
  • CD3 Complex / immunology
  • CD4 Antigens / analysis*
  • CD8 Antigens / analysis*
  • Cells, Cultured
  • Cytotoxicity, Immunologic / drug effects
  • Drug Combinations
  • Granulocyte-Macrophage Colony-Stimulating Factor / pharmacology
  • H-2 Antigens / immunology*
  • Interleukin-1 / pharmacology
  • Interleukin-4 / biosynthesis*
  • Interleukin-7 / physiology*
  • Lymphocyte Activation / drug effects
  • Mice
  • Mice, Inbred C3H
  • Mice, Mutant Strains
  • Receptors, Antigen, T-Cell, alpha-beta / analysis*
  • T-Lymphocyte Subsets / drug effects
  • T-Lymphocyte Subsets / metabolism*
  • Thymus Gland / cytology

Substances

  • Antibodies, Monoclonal
  • CD3 Complex
  • CD4 Antigens
  • CD8 Antigens
  • Drug Combinations
  • H-2 Antigens
  • Interleukin-1
  • Interleukin-7
  • Receptors, Antigen, T-Cell, alpha-beta
  • Interleukin-4
  • Granulocyte-Macrophage Colony-Stimulating Factor