IL-7 enhances Ag-specific human T cell response by increasing expression of IL-2R alpha and gamma chains

J Neuroimmunol. 1999 Apr 1;96(1):101-11. doi: 10.1016/s0165-5728(99)00002-8.

Abstract

Interleukin-7 has demonstrated potent enhancing effects on the growth and differentiation of several immature cell types, including thymocytes, and on survival of resting and antigen activated T cells. In this study, we evaluated the effects of IL-7 on post-thymic antigen-specific T cells from human blood. IL-7 was found to enhance proliferation responses and IFN-gamma secretion of myelin or recall Ag-specific Th1 cells through the selective up-regulation of the IL-2Ralpha and gamma but not beta chains in both an Ag-dependent and Ag-independent manner, but did not affect monocytes, B cells, or NK cells. These functions of IL-7 enhanced the detection of Th1 but not Th2 cell frequency by >2.5 fold, and promoted selection of Ag-specific Th1 cells by the limiting dilution method. Moreover, IL-7 pretreatment conferred increased resistance of CD4+ T cells to CD8+ cell lysis. These studies demonstrate that IL-7 promotes the growth and survival of circulating Ag-specific human Th1 cells through a mechanism that probably involves the gammac common receptor for IL-2 family members that includes IL-7.

Publication types

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

MeSH terms

  • Antigens, CD19 / immunology
  • Antigens, CD19 / metabolism
  • CD11 Antigens / immunology
  • CD11 Antigens / metabolism
  • CD4-Positive T-Lymphocytes / chemistry
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / metabolism
  • CD56 Antigen / immunology
  • CD56 Antigen / metabolism
  • CD8-Positive T-Lymphocytes / chemistry
  • CD8-Positive T-Lymphocytes / cytology
  • CD8-Positive T-Lymphocytes / metabolism*
  • Cell Division / immunology
  • Cell Survival / immunology
  • Clone Cells
  • Humans
  • Immunophenotyping
  • Interferon-gamma / immunology
  • Interferon-gamma / metabolism
  • Interleukin-2 / pharmacology
  • Interleukin-7 / pharmacology*
  • Receptors, Interleukin-2 / analysis
  • Receptors, Interleukin-2 / immunology
  • Receptors, Interleukin-2 / metabolism*
  • Thymus Gland / cytology

Substances

  • Antigens, CD19
  • CD11 Antigens
  • CD56 Antigen
  • Interleukin-2
  • Interleukin-7
  • Receptors, Interleukin-2
  • Interferon-gamma