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. 2015 Feb 3;212(3):445–452. doi: 10.1093/infdis/jiv066

Figure 5.

Figure 5.

Lung myeloid cell subsets in naive and pneumococcal polysaccharide conjugate-vaccinated mice infected with pneumococcus alone or coinfected with influenza virus and pneumococcus. The mice were inoculated intranasally (i.n.) with phosphate-buffered saline (PBS) or 10 plaque-forming units of PR8 influenza and then 1 week later, challenged i.n. with 2 × 106 colony-forming units of A66.1 S. pneumoniae. Lung cell subsets were analyzed 48 hours later by flow cytometry as described in “Material and Methods” section. The cells were defined as follows: neutrophils, Ly6G+CD11b+F4/80; dendritic cells, CD11c+F4/80Ly6G; alveolar macrophages, F4/80+CD11c+CD11bLy6G; monocytes/tissue macrophages, CD11b+F4/80+Ly6G. Each group consisted of 5–7 mice. The data represent means ± SD. *P < .05, **P < .01, ***P < .001, ****P < .0001.