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. 2020 Jun 17;20:126. doi: 10.1186/s12905-020-00972-0

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© The Author(s) 2020

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. 1 — The immune cells related to stages, lymph node metastases, vasoinvasion, and operation. a Circulating Th1, Th2, Th17, and Treg cells in patients with stage I and II; b The levels of four cell types in lymph node metastasis-positive and -negative patients; c The levels of four cell types in vasoinvasion-positive and -negative patients; d UCC 1: Testing the cell in the UCC patients before the operation. UCC2: Testing again 1 month after the operation. UCC3: Testing 6 months after the operation; e CINa: Testing the cell before the operation. CINb: Testing 1 month after the operation. CINc: Testing 6 months after the operation. Compared to the control groups, *: 0.01<P<0.05, **: P ≤ 0.01