Intracellular expression of interleukin-4 and interferon-gamma by a Mycobacterium tuberculosis antigen-stimulated CD4+ CD57+ T-cell subpopulation with memory phenotype in tuberculosis patients

Immunology. 2004 Jan;111(1):100-6. doi: 10.1111/j.1365-2567.2003.01785.x.

Abstract

In some chronic pathological conditions, antigen persistence activates and expands the CD4+ CD57+ T-cell subset. The host immune response against tuberculosis infection is maintained through the continuous presence of antigen-stimulated effector/memory helper T cells. To determine whether CD4+ CD57+ T cells were also expanded in human tuberculosis, we analysed (by flow cytometry) the phenotype of peripheral blood CD4+ T cells from 30 tuberculosis patients and 30 healthy controls. We observed a significant increase in the CD4+ CD57+ T-cell subset in tuberculosis patients in comparison to healthy controls (P < 0.001). Most CD4+ CD57+ T cells exhibited a CD28- CD45RO+ CD62L- phenotype, which is associated with memory cells. In vitro, a higher number of antigen-stimulated CD4+ CD57+ T cells produced intracellular interferon-gamma and interleukin-4 compared with antigen-stimulated CD4+ CD57- T cells (P < 0.001). These findings suggest that the majority of CD4+ CD57+ T cells correspond to a phenotype of activated memory T cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antigens, Bacterial / pharmacology*
  • CD4-Positive T-Lymphocytes / immunology*
  • CD57 Antigens / immunology
  • Case-Control Studies
  • Chronic Disease
  • Coculture Techniques
  • Flow Cytometry
  • Humans
  • Immunologic Memory
  • Interferon-gamma / analysis
  • Interferon-gamma / immunology*
  • Interleukin-4 / analysis
  • Interleukin-4 / immunology*
  • Intracellular Fluid / chemistry
  • Intracellular Fluid / immunology
  • Lymphocyte Activation
  • Lymphocyte Count
  • Mycobacterium tuberculosis / immunology*
  • Statistics, Nonparametric
  • Tuberculosis, Pulmonary / immunology*

Substances

  • Antigens, Bacterial
  • CD57 Antigens
  • Interleukin-4
  • Interferon-gamma