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Induction of Alloantigen-specific Anergy in Human Peripheral Blood Mononuclear Cells by Alloantigen Stimulation with Co-stimulatory Signal Blockade
Published on: March 14, 2011
Human lymphokine-activated killer cells suppress pokeweed mitogen-induced immunoglobulin synthesis
H Suzuki1, N Yamashita, M Maruyama
1First Department of Internal Medicine, Toyama Medical and Pharmaceutical University, School of Medicine, Japan.
Insights
Human lymphokine-activated killer (LAK) cells suppress immunoglobulin production. LAK cells kill activated T and B cells, reducing IgG synthesis in peripheral blood mononuclear cells (PBMC).
Area of Science:
- Immunology
- Cell Biology
Background:
- Pokeweed mitogen (PWM) stimulates immunoglobulin synthesis in peripheral blood mononuclear cells (PBMC).
- Lymphokine-activated killer (LAK) cells are immune cells with cytotoxic capabilities.
Purpose of the Study:
- To investigate the effect of LAK cells on PWM-induced immunoglobulin synthesis.
- To determine the mechanism by which LAK cells influence B cell antibody production.
Main Methods:
- In vitro culture of PBMC with recombinant human interleukin-2 (IL-2) to generate LAK cells.
- Assessing the cytotoxic activity of LAK cells against PWM-activated T and B cells.
- Evaluating IgG production in PBMC cultures supplemented with LAK cells.
Main Results:
- LAK cells, induced by IL-2, effectively lysed PWM-activated autologous T and B cells, but not unstimulated lymphocytes.
- CD8(+) and CD16(+) enriched LAK cells significantly suppressed IgG production.
- Control cells cultured without IL-2 showed minimal suppression of IgG synthesis.
Conclusions:
- LAK cells suppress immunoglobulin synthesis through the cytotoxic elimination of activated T and B cells.
- The findings highlight the role of LAK cells in regulating B cell antibody production via cell-mediated cytotoxicity.
Abstract:
The effect of human lymphokine-activated killer (LAK) cells on pokeweed mitogen (PWM) induced immunoglobulin synthesis by autologous peripheral blood mononuclear cells (PBMC) was studied. LAK cells induced by the in vitro culture with recombinant human interleukin-2 (IL-2) lysed PWM-activated autologous T cells and B cells, but did not lyse unstimulated lymphocytes. These effector cells which are capable of killing lymphoblasts were shown to express either CD16 surface markers. When CD8(+)-and CD16(+)-enriched cells isolated from the culture with IL-2 were added to cultures containing autologous PBMC and PWM, marked suppression of the IgG production was observed. In contrast, the control CD8(+)-and CD16(+)-enriched cells isolated from the culture without IL-2 showed a weak suppressive effect on PWM-induced IgG synthesis. These results suggest that LAK cells suppress immunoglobulin synthesis by the cytotoxic elimination of activated T cells and B cells.
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