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. 2019 Aug 29;23:290. doi: 10.1186/s13054-019-2574-7

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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. 6 — Administration with recombinant human IL-26 exaggerated the production of proinflammatory cytokines and chemokines in CLP-induced sepsis. Cytokine and chemokine concentrations in peritoneal lavage fluid (PLF) and blood from septic mice (n = 5) treated with or without recombinant human IL-26 (0.5 μg) were determined by ELISA at 24 h after CLP. Statistical difference was denoted by the horizontal bracket (Mann–Whitney U test)