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. 2018 Nov 24;13:93. doi: 10.1186/s13000-018-0770-4

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© The Author(s). 2018

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. 3 — The comparison of CD8+ and Foxp3+ T cells in residual tumors between pCR and non-pCR patients. There were no significant differences of intratumoral and peritumoral CD8+ cells between pCR and non-pCR cases (a). However, the Foxp3+ T cells, in both intratumoral and peritumoral areas, were significantly lower in pCR patients than in non-pCR (b)