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. 2019 Mar 7;20:51. doi: 10.1186/s12931-019-1015-0

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© The Author(s). 2019

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 4 — Dendritic cell and lymphoid cell airway influx induced by OVA and ODE exposures. BAL fluid from each treatment group was 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 CD11c^hi DC, CD3⁺ T cells, CD19⁺ B cells, 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, ### P < 0.001) as indicated