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. 2022 Jun 7;23:30. doi: 10.1186/s12865-022-00505-4

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© The Author(s) 2022

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 — Effects of long-term cryopreservation on functional T cells-Th1, Th2, Th17(n = 12)and Tfh, Tregs(n = 18).The proportions of IFN-γ⁺Th1,IL-4⁺Th2,IL-17⁺Th17 (A) and CXCR5⁺Tfh (B) in fresh isolated and cryopreserved (1, 3 and 6 mo, respectively) PBMCs. C The proportions of CD4⁺CD25⁺Tregs expressing CD127⁻ or Foxp3⁺. D The frequency of Tregs, actived Tregs, proliferated Tregs after long-term cryopreservation. E Suppressive experiment using the CFSE label PBMCs cocultured with cryopreserved Tregs. F CD45RO⁻Naïve Tregs,CD45RO⁺Tregs in total CD4⁺T cells or in Tregs in fresh isolated and cryopreserved (1, 3 and 6 mo, respectively) PBMCs. *P < 0.05, **P < 0.01,***P < 0.001