Selective generation of CD8+ T-cell clones from the peripheral blood of patients with cutaneous reactions to beta-lactam antibiotics

Br J Dermatol. 1993 Jun;128(6):619-26. doi: 10.1111/j.1365-2133.1993.tb00255.x.

Abstract

The presence, phenotype, and functional characteristics of peripheral blood penicillin-specific T lymphocytes in individuals with cutaneous allergic reactions to penicillin were investigated using in vitro long-term culture techniques. Peripheral blood mononuclear cells from two penicillin-allergic patients were stimulated in vitro with penicillin, and T-cell blasts were clonally expanded by limiting dilution. Seven T-cell clones were derived, all of which were CD3+ CD4- CD8+ HLA-DR+, and produced IL-2 and IFN-gamma upon stimulation. T-cell proliferation required the presence of antigen and autologous, but not allogeneic, antigen-presenting cells. In addition to the parent compound, the T-cell clones also developed a proliferative response to penicilloyl, the major metabolite of penicillin. The cloned T-cell lines were found to exhibit marked suppressor activity for Con A mitogenesis. The observed suppressor activity required cell-to-cell contact, as supernatants from these T-cell clones had no comparable inhibitory effect. These findings indicate that there is a predominance of penicillin-specific CD8+ T cells in the peripheral blood of individuals sensitized to beta-lactam antibiotics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / adverse effects*
  • CD3 Complex / immunology
  • CD4 Antigens / immunology
  • CD8 Antigens / immunology*
  • Cell Communication / immunology
  • Cell Division / immunology
  • Cells, Cultured
  • Clone Cells / immunology
  • Drug Eruptions / immunology*
  • HLA-DR Antigens / immunology
  • Humans
  • Interferon-gamma / biosynthesis
  • Interleukin-2 / biosynthesis
  • T-Lymphocytes / immunology*
  • beta-Lactams

Substances

  • Anti-Bacterial Agents
  • CD3 Complex
  • CD4 Antigens
  • CD8 Antigens
  • HLA-DR Antigens
  • Interleukin-2
  • beta-Lactams
  • Interferon-gamma