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. 2021 Apr 23;4:499. doi: 10.1038/s42003-021-02018-z

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© The Author(s) 2021

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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Fig. 3 — a Tregs were isolated and stimulated with indicated cytokines. FGL2 mRNA was examined by qRT-PCR after 24 h, the concentration of FGL2 in the supernatant was detected by ELISA. b Predicted binding sites of transcription factors STAT1, NF-κB, and C/EBPα on the FGL2 promoter region. c–e Differentially expressed NF-κB (c), STAT1 (d), and C/EBPα (e) genes in Tregs treated with indicated cytokines. Data represent the mean value ± SEM of five individual experiments (n = 5).