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. 2013 Feb;81(2):585–597. doi: 10.1128/IAI.01249-12

Table 3.

Splenocyte subpopulations in mice infected with 104 CFU LVS i.d.a

Cell type and marker(s) % of cells with indicated marker(s) in mouse strain on:
Day 1
Day 6
WT IL-6 KO WT IL-6 KO
B cells
    CD19+ B220+ 33.3 ± 4.4 33.7 ± 2.5 48.5 ± 1.3 54.5 ± 4.7
T cells
    Total α/β TCR+ 52.3 ± 3.2 50.3 ± 6 31 ± 2.5 31.4 ± 3.3
    CD4+ 31.6 ± 3 28.1 ± 4 17.3 ± 4.3 14.7 ± 2.5
    CD8+ 23.6 ± 10.1 20.3 ± 1.9 13.5 ± 3.6 15.0 ± 3
    CD4 CD8 2 ± 0.8 2.4 ± 2 2.2 ± 0.3 1.5 ± 0.4
Macrophages
    CD11b+ CD11c Gr-1 2.9 ± 0.8 4 ± 0.6 3.4 ± 0.5 2.6 ± 1.1
Dendritic cells
    CD11c+ 0.7 ± 0.1 0.9 ± 1.9 2.7 ± 1.5 3.4 ± 2
Neutrophils
    Gr-1hi CD11bhi 6.0 ± 4.4 3.9 ± 2.4 4.6 ± 2.3 2.5 ± 1.5
NK cells
    NK1.1+ 3.6 ± 1.8 3.7 ± 1.4 3.4 ± 0.5 2.3 ± 0.5
a

Wild-type C57BL/6 and IL-6KO mice were infected i.d. with 104 CFU LVS. Groups of three mice from each group were sacrificed on days 1 and 6 after infection, spleens were harvested and pooled, and splenocytes were prepared for analyses by multiparameter flow cytometry. Cells were analyzed on an LSR II cytometer using appropriate single-color compensation and isotype controls; only live nonaggregated cells were included in the analyses. Data represent means ± standard deviations of data combined from three independent experiments.