Figure 6.
cLTα−/− mice exhibit altered lymphocyte profiles in the draining popliteal LN following M. leprae infection in the FP. cB6 (circles) and cLTα−/− (inverted triangles) FP were inoculated with 6 × 103 viable M. leprae. At 3, 6, and 9 months post-infection, popliteal LN from individual mice were harvested and single cell suspensions were prepared. For analysis by flow cytometry, the lymphocyte gate was determined based on forward- and side-scatter parameters. Cell numbers obtained from cB6 (7.18 × 106 ± 4.82 × 106, 1.38 × 107 ± 1.61 × 107, and 4.66 × 106 ± 2.34 × 106, at 3, 6, and 9 months, respectively) and cLTα−/− (2.36 × 106 ± 1.66 × 106, 7.17 × 105 ± 3.76 × 105, and 3.77 × 106 ± 4.15 × 106, at 3, 6, and 9 months, respectively) mice were similar, except at 6 months post-infection when fewer cells were recovered from the deficient mice (P = 0.0152). The percentage of (A) CD3+ and B220+ cells within the lymphocyte gate, (B) CD3+ cells that were CD4+ or CD8+, and (C) CD4+ and CD8+ cells expressing CD44loCD62Lhi (Naïve [Nv]; closed symbols) and CD44hiCD62Llo (Effector; open symbols) were determined. Each graph depicts group means ± SE of 4 to 5 mice per group and is representative of two independent experiments. *P ≤ 0.05; **P ≤ 0.01; ***P ≤ 0.001; ****P ≤ 0.0001. Below each graph, scatter plots demonstrate flow cytometry data and percentages of an individual representative mouse from each group.