Overexpression of IL-15 in vivo enhances Tc1 response, which inhibits allergic inflammation in a murine model of asthma

IL-15, a pleiotropic cytokine, is involved in the inflammatory responses in various infectious and autoimmune diseases. We have recently constructed I L-15-transgenic (Tg) mice, which have an increased number of memory-type CD 8(+) T cells in the peripheral lymphoid tissues. In the present study, we f ound that eosinophilia and Th2-type cytokine production in the airway were severely attenuated in OVA-sensitized IL-15-Tg mice following OVA inhalatio n, IL-15-Tg mice preferentially developed Tc1 responses mediated by CD8(+) T cells after OVA sensitization, and in vivo depletion of CD8+ T cells by a nti-CDS mAb aggravated the allergic airway inflammation in IL-15-Tg mice fo llowing OVA inhalation. Adoptive transfer of CD8(+) T cells from OVA-sensit ized IL-15-Tg mice into normal mice before OVA sensitization suppressed Th2 response to OVA in the normal mice. These results suggest that overexpress ion of IL-15 in vivo suppresses Th2-mediated-allergic airway response via i nduction of CD8(+) T cell-mediated Tc1 response.