Fig. 5.
Lung tissue infiltrates induced by OVA and ODE exposures. Whole lung tissues from each treatment group were processed and analyzed by flow cytometry. Numbers of cells were calculated by multiplying the percentage of cells in respective gate (% of CD45 +cells as analyzed by FACS) multiplied by respective total cells for each mouse. Bar graphs depict means with standard error bars of neutrophils (CD11c−Ly6G+), eosinophils (CD11c−CD11b+Siglec−F+), alveolar macrophages (autoflourescence+CD11c+), conventional CD11chi DC, CD3+ T cells, CD19+ B cells, natural killer (NK) cells (CD3−NK1.1+), ILC2 (LIN−ICOS+ST2+), and ILC3 (LIN−NKp46+). N = 4–6 mice/group. Statistical significance denoted (* P < 0.05, ** P < 0.01, *** P < 0.001) vs. Sal-Sal. Statistical significance denoted (# P < 0.05, ## P < 0.01) as indicated