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. 2022 Sep 28;22:1021. doi: 10.1186/s12885-022-10114-4

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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. 3 — Immunohistochemical staining of CD68⁺, CD3⁺, CD4⁺ and CD8⁺ cell subsets. A subset of 10 cases was stained with CD3, CD4, CD8 and CD68 antibodies to specify the phenotypes of the infiltrating immune cells. In these selected cases, CD8⁺ T cells largely dominated the immune landscape of the TME and outnumbered CD68⁺ macrophages (Created with Biorender, No. FB24AJR43N)