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. 2019 May 9;9:7147. doi: 10.1038/s41598-019-43451-9

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© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Inflammatory cell recruitment into lung tissues after MP infection. The number of cells in BALF collected from mice pre-treated with CYP/saline and injected with 108 colony forming units of MP/saline for 96 h is shown. (A) Total number of cells in BALF. (B) PMNs in BALF. Data are presented as mean ± standard deviation (n = 5–7). MP, Mycoplasma pneumoniae; BALF, bronchoalveolar lavage fluid; CYP, cyclophosphamide; PMN, polymorphonuclear neutrophils; NS + NS, uninfected immunocompetent mice; CYP + NS, uninfected immunocompromised mice; NS + MP, infected immunocompetent mice; CYP + MP, infected immunocompromised mice. ***P < 0.001.