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. 2022 Sep 8;26:44. doi: 10.1186/s40824-022-00290-6

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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. 4 — Activated immune response tests by TAT/CDT/ICB. (a-b) Representative flow cytometry plots showing T cells (a) and Treg cells (b) in the distant tumors from different groups 10 days post-treatment (CT26 tumor model). (c) Proportions of tumor-infiltrating CD8⁺ killer T cells among CD3⁺ cells (CT26 tumor model). Error bars represent mean ± s.d. (n = 3). (d) Proportions of Treg cells in tumor. Error bars represent mean ± s.d. (n = 3). (e) TNF-α level and interferon-γ (IFN-γ) level in mice sera post-various treatments (CT26 tumor model). Note, 1: Control, 2: Anti-PD-L1, 3: ²¹¹At-ATE-MnO₂-BSA, 4: ²¹¹At-ATE-MnO₂-BSA + Anti-PD-L1. P values were calculated by t-test (*P<0.05, **P < 0.01 and ***P < 0.001)