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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. 2 — Comparison of myeloid and lymphoid subsets between AA and Non-AA TNBC tumors. A Representative images of multiplex immunofluorescent staining for two macrophage markers: CD68 and CD206, T cell markers: CD3, CD4 and CD8, and B-cell marker: CD20. B Comparison of the level of the above markers in AA versus Non-AA TNBC tumors