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. 2021 Jul 22;17:74. doi: 10.1186/s13223-021-00577-8

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© The Author(s) 2021

Open AccessThis 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 licence, and indicate if changes were made. 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/4.0/. 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 in a credit line to the data.

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Fig. 6 — Alleviation of allergic inflammation by the adoptive transfer of CD8⁺CD25⁺fork-head box transcription factor (Foxp3)⁺ regulatory T cells (CD8⁺ Tregs) in a murine model of allergic rhinitis (AR). A Number of sneezing. B Number of nasal rubbing. C Number of eosinophils in the nasal lavage fluid (NLF). D eosinophil cation protein (ECP) in the NLF. E interleukin (IL)-4 in the NLF. F IL-5 in the NLF. G IL-13 in the NLF. H IL-10 in the NLF. I Transforming growth factor (TGF)-β in the NLF. Normal, normal group; AR, allergic rhinitis group; Normal CD8⁺ Tregs, treatment of AR mice with normal CD8⁺ Tregs; AR CD8⁺ Tregs, treatment of AR mice with AR CD8⁺ Tregs. The values shown are expressed as mean ± SEM. ****p < 0.0001