4.6 Article

The Immune Landscape of Colorectal Cancer

期刊

CANCERS
卷 13, 期 21, 页码 -

出版社

MDPI
DOI: 10.3390/cancers13215545

关键词

colorectal cancer; multiplex; tumor immunology; immune landscape

类别

资金

  1. Swedish Cancer Society [CAN 2018/772, CAN 2019/0382, CAN 2018/816, CAN 2017/1066]
  2. Lions Cancer Foundation Uppsala
  3. Selanders foundation
  4. P.O. Zetterling Foundation
  5. Swedish Government (SRA CancerUU)
  6. Uppsala University
  7. Region Uppsala

向作者/读者索取更多资源

This study provides a detailed overview of the immune landscape of colorectal cancer by analyzing immune cell subsets in different tumor regions, revealing 'inflamed' and 'desert' groups among therapy-naive patients. Additionally, it identifies the impact of specific immune cell types on survival outcomes in different stages of colon cancer and highlights the repopulation of the immune infiltrate in rectal tumors post radiation.
Simple Summary: We sought to provide a detailed overview of the immune landscape of colorectal cancer in the largest study to date in terms of patient numbers and analyzed immune cell types. We applied a multiplex in situ staining method in combination with an advanced scanning and image analysis pipeline akin to flow cytometry, and analyzed 5968 individual multi-layer images of tissue defining in a total of 39,078,450 cells. We considered the location of immune cells with respect to the stroma, and tumor cell compartment and tumor regions in the central part or the invasive margin. To the best of our knowledge, this study is the first comprehensive spatial description of the immune landscape in colorectal cancer using a large population-based cohort and a multiplex immune cell identification. While the clinical importance of CD8+ and CD3+ cells in colorectal cancer (CRC) is well established, the impact of other immune cell subsets is less well described. We sought to provide a detailed overview of the immune landscape of CRC in the largest study to date in terms of patient numbers and in situ analyzed immune cell types. Tissue microarrays from 536 patients were stained using multiplexed immunofluorescence panels, and fifteen immune cell subclasses, representing adaptive and innate immunity, were analyzed. Overall, therapy-naive CRC patients clustered into an 'inflamed' and a 'desert' group. Most T cell subsets and M2 macrophages were enriched in the right colon (p-values 0.046-0.004), while pDC cells were in the rectum (p = 0.008). Elderly patients had higher infiltration of M2 macrophages (p = 0.024). CD8+ cells were linked to improved survival in colon cancer stages I-III (q = 0.014), while CD4+ cells had the strongest impact on overall survival in metastatic CRC (q = 0.031). Finally, we demonstrated repopulation of the immune infiltrate in rectal tumors post radiation, following an initial radiation-induced depletion. This study provides a detailed analysis of the in situ immune landscape of CRC paving the way for better diagnostics and providing hints to better target the immune microenvironment.

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