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. 2024 Sep 3;10:79. doi: 10.1038/s41522-024-00558-w

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

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Fig. 1 — A Percentage of pulmonary NK cells and (B) T-cells following NK1.1 depletion. C Representative gating strategy. D K. pneumoniae lung burden at 48 h. post-infection in binge-on-chronic alcohol-treated mice. E Circulating levels of surfactant protein D1 (SPD-1) in binge-on-chronic alcohol-treated mice 48 h. post infection. F Circulating levels of intestinal fatty acid binding protein (iFABP) in binge-on-chronic alcohol-treated mice 48 h. post-infection; p values are indicated in the figure by one‐way ANOVA with Sidak’s multiple comparison. N = 10–12 mice/group derived from 2 independent experiments. N = 4–6 mice/group for the alcohol-fed or pair-fed with NK depletion derived from 1 experiment.