Figure 2
Figure 2. HBZ-Tg mice show decreased immune response to primary and secondary infection with LM. Bacterial loads of spleens from mice challenged with LM in primary (A) and secondary (B) infection are shown. (C) Concentrations of IFN-γ, TNF-α, IL-2, IL-6, and IL-12 in serum and IL-10 in homogenized spleen supernatant from the secondarily infected mice. (D) Cytokine production by CD4 T cells from secondarily infected mice. Mice were immunized as shown in panel B. CD4 T cells were stimulated ex vivo with mAbs to CD3 and CD28 or with LM-infected WT-BMDMs. Bars represent the mean ± SD of all mice per genotype. Two independent experiments have been performed; representative results are shown. *P < .05 by Student t test. N.D. indicates not detected.

HBZ-Tg mice show decreased immune response to primary and secondary infection with LM. Bacterial loads of spleens from mice challenged with LM in primary (A) and secondary (B) infection are shown. (C) Concentrations of IFN-γ, TNF-α, IL-2, IL-6, and IL-12 in serum and IL-10 in homogenized spleen supernatant from the secondarily infected mice. (D) Cytokine production by CD4 T cells from secondarily infected mice. Mice were immunized as shown in panel B. CD4 T cells were stimulated ex vivo with mAbs to CD3 and CD28 or with LM-infected WT-BMDMs. Bars represent the mean ± SD of all mice per genotype. Two independent experiments have been performed; representative results are shown. *P < .05 by Student t test. N.D. indicates not detected.

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