(A) After overnight stimulation with CSA, the cells isolated from the lungs of infected C57BL/6 animals were surface stained with CD11b (APC/Cy7), CD11c (APC), CD80 (FITC) and MHC-II (PE) followed by flow cytometry analysis. Gating strategy employed and flow cytometry dot plots of CD11b+CD80+, CD11b+MHCII+, CD11c+CD80+, CD11c+MHCII+ cells in the lungs of infected mice (B–E) Percentage of (B) CD11b+CD80+, (C) CD11b+MHCII+, (D) CD11c+CD80+ and (E) CD11c+MHCII+ cells in the lungs. (F–I) Percentage of CD11b+CD80+, CD11b+MHCII+, CD11c+CD80+, CD11c+MHCII+ cells in the spleen of infected mice. Data is representative of two independent experiments with five mice per group. Each graph represents mean ± SD (n = 5). ***p<0.0005.
Figure 7—source data 1. AGK2 treatment enhances macrophage stimulation in the lungs and spleen of infected animals.