Study of the biological activities of toxic shock syndrome toxin-1: II. Induction of the proliferative response and the interleukin 2 production by T cells from human …

T Uchiyama, Y Kamagata, XJ Yan… - Clinical and …, 1987 - ncbi.nlm.nih.gov
T Uchiyama, Y Kamagata, XJ Yan, M Kohno, M Yoshioka, H Fujikawa, H Igarashi, M Okubo…
Clinical and experimental immunology, 1987ncbi.nlm.nih.gov
Toxic shock syndrome toxin-1 (TSST-1) is an exotoxin produced by Staphylococcus aureus
isolated from patients with toxic shock syndrome. We investigated the proliferative response
of human lymphocytes and their interleukin 2 (IL-2) production after stimulation with TSST-1
in vitro. Human cord blood mononuclear cells (HCBM) and human peripheral blood
mononuclear cells (HPBM) could proliferate with TSST-1 stimulation. T cell-depleted HPBM
showed only a marginal response to this toxin. A IL-2-like factor with a molecular weight of …
Abstract
Toxic shock syndrome toxin-1 (TSST-1) is an exotoxin produced by Staphylococcus aureus isolated from patients with toxic shock syndrome. We investigated the proliferative response of human lymphocytes and their interleukin 2 (IL-2) production after stimulation with TSST-1 in vitro. Human cord blood mononuclear cells (HCBM) and human peripheral blood mononuclear cells (HPBM) could proliferate with TSST-1 stimulation. T cell-depleted HPBM showed only a marginal response to this toxin. A IL-2-like factor with a molecular weight of 15-18 kD was obtained from the supernatants of TSST-1-stimulated HPBM cultures. The factor was absorbed by CTLL-2 cells but not by T cell-depleted murine spleen cells, indicating that it is IL-2. HPBM are very sensitive to TSST-1: a low concentration of TSST-1 (0· 01 ng/ml in 36 h stimulation) and a short period of stimulation (8 h at 10 ng/ml of the toxin) were fully effective for HPBM to produce substantial amounts of IL-2. Removal of T cells abrogated the TSST-1-induced IL-2 production by HPBM. Reconstituted cell cultures of nylon wool column-passed T cells and macrophages produced IL-2 by TSST-1 stimulation and, furthermore, the accessory activity of the macrophages could be partially replaced by a macrophage-derived factor containing interleukin 1. These findings indicate that T cells require macrophages or IL-1 for TSST-1-induced production of IL-2. The roles of lymphokines, including IL-2, in the development of this illness are discussed.
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