Figure 5
Figure 5. Ruxolitinib reduces the numbers of activated and LCMV-specific CD8+ T cells in LCMV-infected Prf1−∕− mice. Mice treated with PBS, ruxolitinib, LCMV, and LCMV + ruxolitinib (L+R) were euthanized on day 9 postinfection. Splenocytes were stained using anti-CD4, CD8, CD44 antibodies and fluorochrome-conjugated MHC class I tetramer (Dbgp33). (A) Representative flow cytometric plots showing the percentages of CD4+, CD8+, CD8+CD44+ (top and middle panels, gated on live splenocytes) and CD8+gp33+ (bottom panels, gated on CD8+CD44+ cells) cells from a representative mouse in each group. (B) Percentage and (C) absolute number of splenic CD8+, CD8+CD44+, and CD8+CD44+gp33+ cells. Data are shown as mean ± SD and are representative of 4 independent experiments. *P < .05.

Ruxolitinib reduces the numbers of activated and LCMV-specific CD8+ T cells in LCMV-infected Prf1−∕− mice. Mice treated with PBS, ruxolitinib, LCMV, and LCMV + ruxolitinib (L+R) were euthanized on day 9 postinfection. Splenocytes were stained using anti-CD4, CD8, CD44 antibodies and fluorochrome-conjugated MHC class I tetramer (Dbgp33). (A) Representative flow cytometric plots showing the percentages of CD4+, CD8+, CD8+CD44+ (top and middle panels, gated on live splenocytes) and CD8+gp33+ (bottom panels, gated on CD8+CD44+ cells) cells from a representative mouse in each group. (B) Percentage and (C) absolute number of splenic CD8+, CD8+CD44+, and CD8+CD44+gp33+ cells. Data are shown as mean ± SD and are representative of 4 independent experiments. *P < .05.

Close Modal

or Create an Account

Close Modal
Close Modal