Journal Article DKFZ-2018-01473

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Topography of cancer-associated immune cells in human solid tumors.

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2018
eLife Sciences Publications Cambridge

eLife 7, e36967 () [10.7554/eLife.36967]
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Abstract: Lymphoid and myeloid cells are abundant in the tumor microenvironment, can be quantified by immunohistochemistry and shape the disease course of human solid tumors. Yet, there is no comprehensive understanding of spatial immune infiltration patterns (topography) across cancer entities and across various immune cell types. In this study, we systematically measure the topography of multiple immune cell types in 965 histological tissue slides from N = 177 patients in a pan-cancer cohort. We provide a definition of inflamed (hot), non-inflamed (cold) and immune excluded patterns and investigate how these patterns differ between immune cell types and between cancer types. In an independent cohort of N = 287 colorectal cancer patients, we show that hot, cold and excluded topographies for effector lymphocytes (CD8) and tumor-associated macrophages (CD163) alone are not prognostic, but that a bivariate classification system can stratify patients. Our study adds evidence to consider immune topographies as biomarkers for patients with solid tumors.

Classification:

Contributing Institute(s):
  1. D120 Angewandte Tumor-Immunität (D120)
  2. KKE Dermatoonkologie (G300)
  3. C020 Epidemiologie von Krebs (C020)
  4. C070 Klinische Epidemiologie und Alternf. (C070)
  5. Präventive Onkologie (G110)
  6. DKTK Heidelberg (L101)
Research Program(s):
  1. 314 - Tumor immunology (POF3-314) (POF3-314)

Appears in the scientific report 2018
Database coverage:
Medline ; Creative Commons Attribution CC BY (No Version) ; DOAJ ; BIOSIS Previews ; DOAJ Seal ; IF >= 5 ; JCR ; NCBI Molecular Biology Database ; SCOPUS ; Science Citation Index Expanded ; Thomson Reuters Master Journal List ; Web of Science Core Collection
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Document types > Articles > Journal Article
Institute Collections > D120
Institute Collections > C020
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 Record created 2018-09-20, last modified 2024-02-29


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