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. 2021 Dec 14;23:113. doi: 10.1186/s13058-021-01493-w

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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. 3 — Comparison of T-cells status and Regulatory T-Cell population in AA versus Non-AA TNBC. A Representative image of multiplex immunofluorescent staining for CD3, Ki67 and GzB markers B Comparison of Ki67 and GzB in T-cells of AA vs Non-AA TNBC tumors. C Schema of activation status of T cells. D Comparison of the activation status of T-Cell in AA vs Non-AA TNBC tumors. E Representative image of multiplex immunofluorescent staining for CD4 and FOXP3 markers. F Comparison of regulatory T-cell population in AA versus Non-AA TNBC tumors