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Single-cell transcriptomic landscape reveals tumor specific innate lymphoid cells associated with colorectal cancer progression
Innate lymphoid cells (ILCs) are tissue-resident lymphocytes differing from conventional T lymphocytes in having no antigen-specific receptors. ILCs include natural killer (NK) cells, helper-like ILC1s, ILC2s, and ILC3s, and lymphoid tissue-inducer (LTi) cells. Tumor ILCs are frequently found in var...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8385246/ https://www.ncbi.nlm.nih.gov/pubmed/34467243 http://dx.doi.org/10.1016/j.xcrm.2021.100353 |
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author | Qi, Jingjing Crinier, Adeline Escalière, Bertrand Ye, Youqiong Wang, Zhengting Zhang, Tianyu Batista, Luciana Liu, Hongzhi Hong, Liwen Wu, Ningbo Zhang, Mingnan Chen, Lei Liu, Yingbin Shen, Lei Narni-Mancinelli, Emilie Vivier, Eric Su, Bing |
author_facet | Qi, Jingjing Crinier, Adeline Escalière, Bertrand Ye, Youqiong Wang, Zhengting Zhang, Tianyu Batista, Luciana Liu, Hongzhi Hong, Liwen Wu, Ningbo Zhang, Mingnan Chen, Lei Liu, Yingbin Shen, Lei Narni-Mancinelli, Emilie Vivier, Eric Su, Bing |
author_sort | Qi, Jingjing |
collection | PubMed |
description | Innate lymphoid cells (ILCs) are tissue-resident lymphocytes differing from conventional T lymphocytes in having no antigen-specific receptors. ILCs include natural killer (NK) cells, helper-like ILC1s, ILC2s, and ILC3s, and lymphoid tissue-inducer (LTi) cells. Tumor ILCs are frequently found in various cancers, but their roles in cancer immunity and immunotherapy remain largely unclear. We report here the single-cell characterization of blood and gut helper-like ILC subsets in healthy conditions and in colorectal cancer (CRC). The healthy gut contains ILC1s, ILC3s, and ILC3/NKs, but no ILC2s. Additional tumor-specific ILC1-like and ILC2 subsets were identified in CRC patients. Signaling lymphocytic activation molecule family member 1 (SLAMF1) was found to be selectively expressed on tumor-specific ILCs, and higher levels of SLAMF1(+) ILCs were observed in the blood of CRC patients. The SLAMF1-high group of CRC patients had a significantly higher survival rate than the SLAMF1-low group, suggesting that SLAMF1 is an anti-tumor biomarker in CRC. |
format | Online Article Text |
id | pubmed-8385246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-83852462021-08-30 Single-cell transcriptomic landscape reveals tumor specific innate lymphoid cells associated with colorectal cancer progression Qi, Jingjing Crinier, Adeline Escalière, Bertrand Ye, Youqiong Wang, Zhengting Zhang, Tianyu Batista, Luciana Liu, Hongzhi Hong, Liwen Wu, Ningbo Zhang, Mingnan Chen, Lei Liu, Yingbin Shen, Lei Narni-Mancinelli, Emilie Vivier, Eric Su, Bing Cell Rep Med Article Innate lymphoid cells (ILCs) are tissue-resident lymphocytes differing from conventional T lymphocytes in having no antigen-specific receptors. ILCs include natural killer (NK) cells, helper-like ILC1s, ILC2s, and ILC3s, and lymphoid tissue-inducer (LTi) cells. Tumor ILCs are frequently found in various cancers, but their roles in cancer immunity and immunotherapy remain largely unclear. We report here the single-cell characterization of blood and gut helper-like ILC subsets in healthy conditions and in colorectal cancer (CRC). The healthy gut contains ILC1s, ILC3s, and ILC3/NKs, but no ILC2s. Additional tumor-specific ILC1-like and ILC2 subsets were identified in CRC patients. Signaling lymphocytic activation molecule family member 1 (SLAMF1) was found to be selectively expressed on tumor-specific ILCs, and higher levels of SLAMF1(+) ILCs were observed in the blood of CRC patients. The SLAMF1-high group of CRC patients had a significantly higher survival rate than the SLAMF1-low group, suggesting that SLAMF1 is an anti-tumor biomarker in CRC. Elsevier 2021-07-27 /pmc/articles/PMC8385246/ /pubmed/34467243 http://dx.doi.org/10.1016/j.xcrm.2021.100353 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Qi, Jingjing Crinier, Adeline Escalière, Bertrand Ye, Youqiong Wang, Zhengting Zhang, Tianyu Batista, Luciana Liu, Hongzhi Hong, Liwen Wu, Ningbo Zhang, Mingnan Chen, Lei Liu, Yingbin Shen, Lei Narni-Mancinelli, Emilie Vivier, Eric Su, Bing Single-cell transcriptomic landscape reveals tumor specific innate lymphoid cells associated with colorectal cancer progression |
title | Single-cell transcriptomic landscape reveals tumor specific innate lymphoid cells associated with colorectal cancer progression |
title_full | Single-cell transcriptomic landscape reveals tumor specific innate lymphoid cells associated with colorectal cancer progression |
title_fullStr | Single-cell transcriptomic landscape reveals tumor specific innate lymphoid cells associated with colorectal cancer progression |
title_full_unstemmed | Single-cell transcriptomic landscape reveals tumor specific innate lymphoid cells associated with colorectal cancer progression |
title_short | Single-cell transcriptomic landscape reveals tumor specific innate lymphoid cells associated with colorectal cancer progression |
title_sort | single-cell transcriptomic landscape reveals tumor specific innate lymphoid cells associated with colorectal cancer progression |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8385246/ https://www.ncbi.nlm.nih.gov/pubmed/34467243 http://dx.doi.org/10.1016/j.xcrm.2021.100353 |
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