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Innate immunity in pancreatic cancer: Lineage tracing and function
Increasingly, patients with gastrointestinal tumors can benefit from immunotherapy, but not patients with pancreatic cancer. While this lack of benefit has been attributed to lower T-cell infiltration in pancreatic cancer, other studies have demonstrated the presence of numerous T cells in pancreati...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884680/ https://www.ncbi.nlm.nih.gov/pubmed/36726981 http://dx.doi.org/10.3389/fimmu.2022.1081919 |
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author | Ye, Longyun Shi, Saimeng Chen, Wei |
author_facet | Ye, Longyun Shi, Saimeng Chen, Wei |
author_sort | Ye, Longyun |
collection | PubMed |
description | Increasingly, patients with gastrointestinal tumors can benefit from immunotherapy, but not patients with pancreatic cancer. While this lack of benefit has been attributed to lower T-cell infiltration in pancreatic cancer, other studies have demonstrated the presence of numerous T cells in pancreatic cancer, suggesting another mechanism for the poor efficacy of immunotherapy. Single-cell RNA sequencing studies on the pancreatic cancer immune microenvironment have demonstrated the predominance of innate immune cells (e.g., macrophages, dendritic cells, mast cells, and innate immune lymphoid cells). Therefore, in-depth research on the source and function of innate immune lymphocytes in pancreatic cancer could guide pancreatic cancer immunotherapy. |
format | Online Article Text |
id | pubmed-9884680 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98846802023-01-31 Innate immunity in pancreatic cancer: Lineage tracing and function Ye, Longyun Shi, Saimeng Chen, Wei Front Immunol Immunology Increasingly, patients with gastrointestinal tumors can benefit from immunotherapy, but not patients with pancreatic cancer. While this lack of benefit has been attributed to lower T-cell infiltration in pancreatic cancer, other studies have demonstrated the presence of numerous T cells in pancreatic cancer, suggesting another mechanism for the poor efficacy of immunotherapy. Single-cell RNA sequencing studies on the pancreatic cancer immune microenvironment have demonstrated the predominance of innate immune cells (e.g., macrophages, dendritic cells, mast cells, and innate immune lymphoid cells). Therefore, in-depth research on the source and function of innate immune lymphocytes in pancreatic cancer could guide pancreatic cancer immunotherapy. Frontiers Media S.A. 2023-01-16 /pmc/articles/PMC9884680/ /pubmed/36726981 http://dx.doi.org/10.3389/fimmu.2022.1081919 Text en Copyright © 2023 Ye, Shi and Chen https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Ye, Longyun Shi, Saimeng Chen, Wei Innate immunity in pancreatic cancer: Lineage tracing and function |
title | Innate immunity in pancreatic cancer: Lineage tracing and function |
title_full | Innate immunity in pancreatic cancer: Lineage tracing and function |
title_fullStr | Innate immunity in pancreatic cancer: Lineage tracing and function |
title_full_unstemmed | Innate immunity in pancreatic cancer: Lineage tracing and function |
title_short | Innate immunity in pancreatic cancer: Lineage tracing and function |
title_sort | innate immunity in pancreatic cancer: lineage tracing and function |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884680/ https://www.ncbi.nlm.nih.gov/pubmed/36726981 http://dx.doi.org/10.3389/fimmu.2022.1081919 |
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