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. 2019 Sep 5;20:350. doi: 10.1186/s12882-019-1548-y

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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. 5 — Effects of VIP on the proportion of Th17/Treg cells in lymphocytes in vitro. Mouse spleen lymphocytes were separated in a sterile environment, and the experiment was terminated after 72 h of VIP treatment. The fraction of Th17 and Treg cells in each group was detected by flow cytometry. The pseudo-coloured flow cytometry picture represents the cellular distribution of one typical sample from each group. **p < 0.01 compared with LN mice