Figure 4
Figure 4. Splenomegaly is associated with an expansion of relative frequencies of myeloid cells and a relative contraction of lymphoid subsets. (A) Splenomegaly is dose and TLR7 dependent. Splenomegaly was less pronounced in IFNAR−/− or IRF7−/− mice and absent in TLR7−/− mice upon 1 mg/kg per day of R848 treatment. Spleen weight was first normalized to total body weight of each individual mouse and, second, normalized to the spleen weight of mock-treated animals. Error bars indicate 95% confidence intervals. (B) The prevalence of CD11b+ macrophages, CD11c+ dendritic cells, and CD11b+/Gr-1+ neutrophils was increased, whereas that of lymphoid subpopulations was decreased as compared with mock-treated animals (C). Mice were treated with PBS or 1 mg/kg per day R848 for 7 days. Splenocytes were stained with indicated antibodies and relative numbers were assessed by flow cytometry. Error bars indicate standard error. N ≥ 3.

Splenomegaly is associated with an expansion of relative frequencies of myeloid cells and a relative contraction of lymphoid subsets. (A) Splenomegaly is dose and TLR7 dependent. Splenomegaly was less pronounced in IFNAR−/− or IRF7−/− mice and absent in TLR7−/− mice upon 1 mg/kg per day of R848 treatment. Spleen weight was first normalized to total body weight of each individual mouse and, second, normalized to the spleen weight of mock-treated animals. Error bars indicate 95% confidence intervals. (B) The prevalence of CD11b+ macrophages, CD11c+ dendritic cells, and CD11b+/Gr-1+ neutrophils was increased, whereas that of lymphoid subpopulations was decreased as compared with mock-treated animals (C). Mice were treated with PBS or 1 mg/kg per day R848 for 7 days. Splenocytes were stained with indicated antibodies and relative numbers were assessed by flow cytometry. Error bars indicate standard error. N ≥ 3.

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