Figure 2.
Excess IL-18 acts on expanding T cells to drive virus-induced hyperinflammation. (A) Mice were infected with LCMV-Arm and assessed for IL-18R1 expression on splenic CD8+ and CD4+ T cells. (B) Representative histograms of IL-18R1 expression on splenic NK, CD4+CD44+, and CD8+CD44+ T lymphocytes of uninfected mice of the indicated genotypes. (C) Mice of the indicated genotypes were infected with LCMV-Arm and assessed for weight loss, splenomegaly, anemia, and serum IFNg and IL-18. Dashed horizontal lines represent the median values of infected CD4Cre-Il18r1fl/fl mice. Weight statistical significance compares Il18tg;CD4Cre-Il18r1fl/fl; and Il18tg;CD4Cre+Il18r1fl/fl mice. Data are representative of 2 independent experiments with a minimum of 3 mice per genotype. *Adjusted P < .05, **P < .01, ***P < .001, ***P < .0001 by unpaired t test on Day 8 values. Significance is only shown for comparisons where adjusted P < .05. Error bars represent SEM.

Excess IL-18 acts on expanding T cells to drive virus-induced hyperinflammation. (A) Mice were infected with LCMV-Arm and assessed for IL-18R1 expression on splenic CD8+ and CD4+ T cells. (B) Representative histograms of IL-18R1 expression on splenic NK, CD4+CD44+, and CD8+CD44+ T lymphocytes of uninfected mice of the indicated genotypes. (C) Mice of the indicated genotypes were infected with LCMV-Arm and assessed for weight loss, splenomegaly, anemia, and serum IFNg and IL-18. Dashed horizontal lines represent the median values of infected CD4Cre-Il18r1fl/fl mice. Weight statistical significance compares Il18tg;CD4Cre-Il18r1fl/fl; and Il18tg;CD4Cre+Il18r1fl/fl mice. Data are representative of 2 independent experiments with a minimum of 3 mice per genotype. *Adjusted P < .05, **P < .01, ***P < .001, ***P < .0001 by unpaired t test on Day 8 values. Significance is only shown for comparisons where adjusted P < .05. Error bars represent SEM.

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