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. 2023 Jul 5;26(2):360. doi: 10.3892/ol.2023.13946

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Copyright: © Wu et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 1. — Classification immune landscape of high- and low-immunity groups in colorectal cancer. (A) The distribution of colorectal patients in high- and low-immunity groups. (B) The Kaplan-Meier curves predict the overall survival in the high- and low-immunity groups. (C) The immune scores, stromal scores and ESTIMATE scores for the high- and low-immunity groups. (D) Distribution of 22 types of immune cells in the high- and low-immunity groups. (E) Heatmap of ESTIMATE scores and immune gene sets for high- and low-immunity groups. *P<0.05, **P<0.01 and ***P<0.001. tSNE, T-distributed stochastic neighbor embedding; TME, tumor microenvironment; H, high; L, low; CD, cluster of differentiation; NK, natural killer; aDCs, activated dendritic cell; pDCs, plasmacytoid dendritic cell; Th, helper T cells; Tfh, follicular helper T cells; iDCs, immature dendritic cells; APC, antigen-presenting cell; HLA, human leukocyte antigen; CCR, chemokine receptor; DCs, dendritic cell; TIL, tumor infiltrating lymphocyte.