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. 2024 Jan 2;43:6. doi: 10.1186/s13046-023-02933-5

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© The Author(s) 2023

Open Access This 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. 16 — TME and spleen immune characterization of K and KL untreated mice: A, B TME immune profile of KRAS^G12D and KRAS^G12D/LKB1^del tumours injected intramuscularly; C, D spleen immune profile of immunocompetent mice bearing KRAS^G12D and KRAS^G12D/LKB1^del tumours; samples from the experiment in Fig. 12 were collected and processed for FACS analysis of lymphoid and myeloid infiltrating immune cells (see Fig. 2 for the gate strategy). One-way and two-way ANOVA were used for statistical analysis (**p < 0.01, ****p < 0.0001). Error bars indicate SD