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J Asthma Allergy Clin Immunol. 2002 Jun;22(2):436-445. Korean. Original Article.
Kim MS , Lee JS , Cho YJ .
Ewha Womans University College of Medicine, Department of Internal Medicine, Korea.

BACKGROUND AND OBJECTIVES: Recently, distinct cytokine-secreting subsets of CD8+ T cells, similar to their CD4+ Th1- and Th2-type counterparts, have been identified. In order to investigate the role of CD8+ T cells in the pathogenesis of allergic asthma, we determined the changes in the proportion of CD3, CD4+ and CD8+ T cells that expressed the IFN-gamma by Dermatophagoides pteronyssinus antigen 2 (Der p2) activation. METHODS: Peripheral blood mononuclear cells (PBMCs) were obtained from mild persistent allergic asthmatic(n=12) and control subjects(n=8) and cultured with Der p2 for 3 days, and then 12-0-tetracanoylphorbol-13-acetate and calcium ionophore were added 4 hours before staining. Surface CD3, CD4 or CD8 with intracytoplasmic IFN-gamma was measured simultaneously by flow cytometry. RESULTS: Comparing asthmatics with control subjects, we found no differences in the percentage of CD3+, CD4+, or CD8+ T cells in PBMCs stimulated with or without Der p2. When PBMCs were cultured in media only, the proportion of cells producing the cytokines IFN-gamma was similar in CD3+, CD4+ cells, but was significantly lower in CD8+ cells of the asthma group compared to the controls. Both CD4+ and CD8+ subsets revealed a similar degree of reduction in IFN-gamma positive cells in the asthma group compared with the controls by the stimulation of Der p2. CONCLUSION: These findings suggest that CD8+ T cells may be important in the pathogenesis of asthmatic inflammation by modulating the production of IFN-gamma.

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